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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">A novel marker, <italic>ARM58</italic>, confers antimony resistance to <italic>Leishmania</italic> spp.<sup><xref ref-type="fn" rid="d32e504">☆</xref></sup></title><author><name sortKey="Nuhs, Andrea" sort="Nuhs, Andrea" uniqKey="Nuhs A" first="Andrea" last="Nühs">Andrea Nühs</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Sch Fer, Carola" sort="Sch Fer, Carola" uniqKey="Sch Fer C" first="Carola" last="Sch Fer">Carola Sch Fer</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Zander, Dorothea" sort="Zander, Dorothea" uniqKey="Zander D" first="Dorothea" last="Zander">Dorothea Zander</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Trube, Leona" sort="Trube, Leona" uniqKey="Trube L" first="Leona" last="Trübe">Leona Trübe</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Tejera Nevado, Paloma" sort="Tejera Nevado, Paloma" uniqKey="Tejera Nevado P" first="Paloma" last="Tejera Nevado">Paloma Tejera Nevado</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Schmidt, Sonja" sort="Schmidt, Sonja" uniqKey="Schmidt S" first="Sonja" last="Schmidt">Sonja Schmidt</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Arevalo, Jorge" sort="Arevalo, Jorge" uniqKey="Arevalo J" first="Jorge" last="Arevalo">Jorge Arevalo</name><affiliation><nlm:aff id="af010">Instituto de Medicina Tropical Alexander von Humboldt, Universidad Peruana Cayetano Heredia, Lima, Peru</nlm:aff></affiliation></author><author><name sortKey="Adaui, Vanessa" sort="Adaui, Vanessa" uniqKey="Adaui V" first="Vanessa" last="Adaui">Vanessa Adaui</name><affiliation><nlm:aff id="af010">Instituto de Medicina Tropical Alexander von Humboldt, Universidad Peruana Cayetano Heredia, Lima, Peru</nlm:aff></affiliation></author><author><name sortKey="Maes, Louis" sort="Maes, Louis" uniqKey="Maes L" first="Louis" last="Maes">Louis Maes</name><affiliation><nlm:aff id="af020">Department of Biomedical Sciences, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium</nlm:aff></affiliation></author><author><name sortKey="Dujardin, Jean Claude" sort="Dujardin, Jean Claude" uniqKey="Dujardin J" first="Jean-Claude" last="Dujardin">Jean-Claude Dujardin</name><affiliation><nlm:aff id="af015">Instituut voor Tropische Geneeskunde, Antwerp, Belgium</nlm:aff></affiliation><affiliation><nlm:aff id="af020">Department of Biomedical Sciences, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium</nlm:aff></affiliation></author><author><name sortKey="Clos, Joachim" sort="Clos, Joachim" uniqKey="Clos J" first="Joachim" last="Clos">Joachim Clos</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">24596667</idno><idno type="pmc">3940081</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3940081</idno><idno type="RBID">PMC:3940081</idno><idno type="doi">10.1016/j.ijpddr.2013.11.004</idno><date when="2013">2013</date><idno type="wicri:Area/Pmc/Corpus">000380</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">A novel marker, <italic>ARM58</italic>, confers antimony resistance to <italic>Leishmania</italic> spp.<sup><xref ref-type="fn" rid="d32e504">☆</xref></sup></title><author><name sortKey="Nuhs, Andrea" sort="Nuhs, Andrea" uniqKey="Nuhs A" first="Andrea" last="Nühs">Andrea Nühs</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Sch Fer, Carola" sort="Sch Fer, Carola" uniqKey="Sch Fer C" first="Carola" last="Sch Fer">Carola Sch Fer</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Zander, Dorothea" sort="Zander, Dorothea" uniqKey="Zander D" first="Dorothea" last="Zander">Dorothea Zander</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Trube, Leona" sort="Trube, Leona" uniqKey="Trube L" first="Leona" last="Trübe">Leona Trübe</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Tejera Nevado, Paloma" sort="Tejera Nevado, Paloma" uniqKey="Tejera Nevado P" first="Paloma" last="Tejera Nevado">Paloma Tejera Nevado</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Schmidt, Sonja" sort="Schmidt, Sonja" uniqKey="Schmidt S" first="Sonja" last="Schmidt">Sonja Schmidt</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author><author><name sortKey="Arevalo, Jorge" sort="Arevalo, Jorge" uniqKey="Arevalo J" first="Jorge" last="Arevalo">Jorge Arevalo</name><affiliation><nlm:aff id="af010">Instituto de Medicina Tropical Alexander von Humboldt, Universidad Peruana Cayetano Heredia, Lima, Peru</nlm:aff></affiliation></author><author><name sortKey="Adaui, Vanessa" sort="Adaui, Vanessa" uniqKey="Adaui V" first="Vanessa" last="Adaui">Vanessa Adaui</name><affiliation><nlm:aff id="af010">Instituto de Medicina Tropical Alexander von Humboldt, Universidad Peruana Cayetano Heredia, Lima, Peru</nlm:aff></affiliation></author><author><name sortKey="Maes, Louis" sort="Maes, Louis" uniqKey="Maes L" first="Louis" last="Maes">Louis Maes</name><affiliation><nlm:aff id="af020">Department of Biomedical Sciences, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium</nlm:aff></affiliation></author><author><name sortKey="Dujardin, Jean Claude" sort="Dujardin, Jean Claude" uniqKey="Dujardin J" first="Jean-Claude" last="Dujardin">Jean-Claude Dujardin</name><affiliation><nlm:aff id="af015">Instituut voor Tropische Geneeskunde, Antwerp, Belgium</nlm:aff></affiliation><affiliation><nlm:aff id="af020">Department of Biomedical Sciences, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium</nlm:aff></affiliation></author><author><name sortKey="Clos, Joachim" sort="Clos, Joachim" uniqKey="Clos J" first="Joachim" last="Clos">Joachim Clos</name><affiliation><nlm:aff id="af005">Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</nlm:aff></affiliation></author></analytic><series><title level="j">International Journal for Parasitology: Drugs and Drug Resistance</title><idno type="eISSN">2211-3207</idno><imprint><date when="2013">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><title>Graphical abstract</title><fig id="f0025" position="anchor"><graphic xlink:href="fx1"></graphic></fig></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Adaui, V" uniqKey="Adaui V">V. Adaui</name></author><author><name sortKey="Castillo, D" uniqKey="Castillo D">D. Castillo</name></author><author><name sortKey="Zimic, M" uniqKey="Zimic M">M. Zimic</name></author><author><name sortKey="Gutierrez, A" uniqKey="Gutierrez A">A. Gutierrez</name></author><author><name sortKey="Decuypere, S" uniqKey="Decuypere S">S. Decuypere</name></author><author><name sortKey="Vanaerschot, M" uniqKey="Vanaerschot M">M. Vanaerschot</name></author><author><name sortKey="De Doncker, S" uniqKey="De Doncker S">S. De Doncker</name></author><author><name sortKey="Schnorbusch, K" uniqKey="Schnorbusch K">K. Schnorbusch</name></author><author><name sortKey="Maes, I" uniqKey="Maes I">I. Maes</name></author><author><name sortKey="Van Der Auwera, G" uniqKey="Van Der Auwera G">G. Van der Auwera</name></author><author><name sortKey="Maes, L" uniqKey="Maes L">L. Maes</name></author><author><name sortKey="Llanos Cuentas, A" uniqKey="Llanos Cuentas A">A. Llanos-Cuentas</name></author><author><name sortKey="Arevalo, J" uniqKey="Arevalo J">J. Arevalo</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Adaui, V" uniqKey="Adaui V">V. Adaui</name></author><author><name sortKey="Maes, I" uniqKey="Maes I">I. Maes</name></author><author><name sortKey="Huyse, T" uniqKey="Huyse T">T. Huyse</name></author><author><name sortKey="Van Den Broeck, F" uniqKey="Van Den Broeck F">F. Van den Broeck</name></author><author><name sortKey="Talledo, M" uniqKey="Talledo M">M. Talledo</name></author><author><name sortKey="Kuhls, K" uniqKey="Kuhls K">K. Kuhls</name></author><author><name sortKey="De Doncker, S" uniqKey="De Doncker S">S. De Doncker</name></author><author><name sortKey="Maes, L" uniqKey="Maes L">L. Maes</name></author><author><name sortKey="Llanos Cuentas, A" uniqKey="Llanos Cuentas A">A. Llanos-Cuentas</name></author><author><name sortKey="Schonian, G" uniqKey="Schonian G">G. Schonian</name></author><author><name sortKey="Arevalo, J" uniqKey="Arevalo J">J. Arevalo</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Adaui, V" uniqKey="Adaui V">V. Adaui</name></author><author><name sortKey="Schnorbusch, K" uniqKey="Schnorbusch K">K. Schnorbusch</name></author><author><name sortKey="Zimic, M" uniqKey="Zimic M">M. Zimic</name></author><author><name sortKey="Gutierrez, A" uniqKey="Gutierrez A">A. Gutierrez</name></author><author><name sortKey="Decuypere, S" uniqKey="Decuypere S">S. Decuypere</name></author><author><name sortKey="Vanaerschot, M" uniqKey="Vanaerschot M">M. Vanaerschot</name></author><author><name sortKey="De Doncker, S" uniqKey="De Doncker S">S. DE Doncker</name></author><author><name sortKey="Maes, I" uniqKey="Maes I">I. Maes</name></author><author><name sortKey="Llanos Cuentas, A" uniqKey="Llanos Cuentas A">A. Llanos-Cuentas</name></author><author><name sortKey="Chappuis, F" uniqKey="Chappuis F">F. Chappuis</name></author><author><name sortKey="Arevalo, J" uniqKey="Arevalo J">J. Arevalo</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Alvar, J" uniqKey="Alvar J">J. Alvar</name></author><author><name sortKey="Velez, I D" uniqKey="Velez I">I.D. Velez</name></author><author><name sortKey="Bern, C" uniqKey="Bern C">C. Bern</name></author><author><name sortKey="Herrero, M" uniqKey="Herrero M">M. Herrero</name></author><author><name sortKey="Desjeux, P" uniqKey="Desjeux P">P. Desjeux</name></author><author><name sortKey="Cano, J" uniqKey="Cano J">J. Cano</name></author><author><name sortKey="Jannin, J" uniqKey="Jannin J">J. Jannin</name></author><author><name sortKey="Den Boer, M" uniqKey="Den Boer M">M. den Boer</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Arevalo, J" uniqKey="Arevalo J">J. Arevalo</name></author><author><name sortKey="Ramirez, L" uniqKey="Ramirez L">L. Ramirez</name></author><author><name sortKey="Adaui, V" uniqKey="Adaui V">V. Adaui</name></author><author><name sortKey="Zimic, M" uniqKey="Zimic M">M. Zimic</name></author><author><name sortKey="Tulliano, G" uniqKey="Tulliano G">G. Tulliano</name></author><author><name sortKey="Miranda Verastegui, C" uniqKey="Miranda Verastegui C">C. Miranda-Verastegui</name></author><author><name sortKey="Lazo, M" uniqKey="Lazo M">M. Lazo</name></author><author><name sortKey="Loayza Muro, R" uniqKey="Loayza Muro R">R. Loayza-Muro</name></author><author><name sortKey="De Doncker, S" uniqKey="De Doncker S">S. De Doncker</name></author><author><name sortKey="Maurer, A" uniqKey="Maurer A">A. Maurer</name></author><author><name sortKey="Chappuis, F" uniqKey="Chappuis F">F. Chappuis</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author><author><name sortKey="Llanos Cuentas, A" uniqKey="Llanos Cuentas A">A. Llanos-Cuentas</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Azeredo Coutinho, R B" uniqKey="Azeredo Coutinho R">R.B. Azeredo-Coutinho</name></author><author><name sortKey="Mendonca, S C" uniqKey="Mendonca S">S.C. Mendonca</name></author><author><name sortKey="Callahan, H" uniqKey="Callahan H">H. Callahan</name></author><author><name sortKey="Portal, A C" uniqKey="Portal A">A.C. Portal</name></author><author><name sortKey="Max, G" uniqKey="Max G">G. Max</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Beverley, S M" uniqKey="Beverley S">S.M. Beverley</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Brochu, C" uniqKey="Brochu C">C. Brochu</name></author><author><name sortKey="Wang, J" uniqKey="Wang J">J. Wang</name></author><author><name sortKey="Roy, G" uniqKey="Roy G">G. Roy</name></author><author><name sortKey="Messier, N" uniqKey="Messier N">N. Messier</name></author><author><name sortKey="Wang, X Y" uniqKey="Wang X">X.Y. Wang</name></author><author><name sortKey="Saravia, N G" uniqKey="Saravia N">N.G. Saravia</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Brochu, C" uniqKey="Brochu C">C. Brochu</name></author><author><name sortKey="Haimeur, A" uniqKey="Haimeur A">A. Haimeur</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Choudhury, K" uniqKey="Choudhury K">K. Choudhury</name></author><author><name sortKey="Zander, D" uniqKey="Zander D">D. Zander</name></author><author><name sortKey="Kube, M" uniqKey="Kube M">M. Kube</name></author><author><name sortKey="Reinhardt, R" uniqKey="Reinhardt R">R. Reinhardt</name></author><author><name sortKey="Clos, J" uniqKey="Clos J">J. Clos</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Clayton, C E" uniqKey="Clayton C">C.E. Clayton</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Clayton, C E" uniqKey="Clayton C">C.E. Clayton</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Clos, J" uniqKey="Clos J">J. Clos</name></author><author><name sortKey="Choudhury, K" uniqKey="Choudhury K">K. Choudhury</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Croft, S L" uniqKey="Croft S">S.L. Croft</name></author><author><name sortKey="Sundar, S" uniqKey="Sundar S">S. Sundar</name></author><author><name sortKey="Fairlamb, A H" uniqKey="Fairlamb A">A.H. Fairlamb</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Garin, Y J" uniqKey="Garin Y">Y.J. Garin</name></author><author><name sortKey="Sulahian, A" uniqKey="Sulahian A">A. Sulahian</name></author><author><name sortKey="Pratlong, F" uniqKey="Pratlong F">F. Pratlong</name></author><author><name sortKey="Meneceur, P" uniqKey="Meneceur P">P. Meneceur</name></author><author><name sortKey="Gangneux, J P" uniqKey="Gangneux J">J.P. Gangneux</name></author><author><name sortKey="Prina, E" uniqKey="Prina E">E. Prina</name></author><author><name sortKey="Dedet, J P" uniqKey="Dedet J">J.P. Dedet</name></author><author><name sortKey="Derouin, F" uniqKey="Derouin F">F. Derouin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Gooley, P R" uniqKey="Gooley P">P.R. Gooley</name></author><author><name sortKey="Mertens, H D" uniqKey="Mertens H">H.D. Mertens</name></author><author><name sortKey="Tull, D" uniqKey="Tull D">D. Tull</name></author><author><name sortKey="Mcconville, M J" uniqKey="Mcconville M">M.J. McConville</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Gourbal, B" uniqKey="Gourbal B">B. Gourbal</name></author><author><name sortKey="Sonuc, N" uniqKey="Sonuc N">N. Sonuc</name></author><author><name sortKey="Bhattacharjee, H" uniqKey="Bhattacharjee H">H. Bhattacharjee</name></author><author><name sortKey="Legare, D" uniqKey="Legare D">D. Legare</name></author><author><name sortKey="Sundar, S" uniqKey="Sundar S">S. Sundar</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author><author><name sortKey="Rosen, B P" uniqKey="Rosen B">B.P. Rosen</name></author><author><name sortKey="Mukhopadhyay, R" uniqKey="Mukhopadhyay R">R. Mukhopadhyay</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Grondin, K" uniqKey="Grondin K">K. Grondin</name></author><author><name sortKey="Haimeur, A" uniqKey="Haimeur A">A. Haimeur</name></author><author><name sortKey="Mukhopadhyay, R" uniqKey="Mukhopadhyay R">R. Mukhopadhyay</name></author><author><name sortKey="Rosen, B P" uniqKey="Rosen B">B.P. Rosen</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Haimeur, A" uniqKey="Haimeur A">A. Haimeur</name></author><author><name sortKey="Guimond, C" uniqKey="Guimond C">C. Guimond</name></author><author><name sortKey="Pilote, S" uniqKey="Pilote S">S. Pilote</name></author><author><name sortKey="Mukhopadhyay, R" uniqKey="Mukhopadhyay R">R. Mukhopadhyay</name></author><author><name sortKey="Rosen, B P" uniqKey="Rosen B">B.P. Rosen</name></author><author><name sortKey="Poulin, R" uniqKey="Poulin R">R. Poulin</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Haimeur, A" uniqKey="Haimeur A">A. Haimeur</name></author><author><name sortKey="Brochu, C" uniqKey="Brochu C">C. Brochu</name></author><author><name sortKey="Genest, P" uniqKey="Genest P">P. Genest</name></author><author><name sortKey="Papadopoulou, B" uniqKey="Papadopoulou B">B. Papadopoulou</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Hofmann, K" uniqKey="Hofmann K">K. Hofmann</name></author><author><name sortKey="Stoffel, W" uniqKey="Stoffel W">W. Stoffel</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Hoyer, C" uniqKey="Hoyer C">C. Hoyer</name></author><author><name sortKey="Mellenthin, K" uniqKey="Mellenthin K">K. Mellenthin</name></author><author><name sortKey="Schilhabel, M" uniqKey="Schilhabel M">M. Schilhabel</name></author><author><name sortKey="Platzer, M" uniqKey="Platzer M">M. Platzer</name></author><author><name sortKey="Clos, J" uniqKey="Clos J">J. Clos</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kapler, G M" uniqKey="Kapler G">G.M. Kapler</name></author><author><name sortKey="Coburn, C M" uniqKey="Coburn C">C.M. Coburn</name></author><author><name sortKey="Beverley, S M" uniqKey="Beverley S">S.M. Beverley</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kelly, J M" uniqKey="Kelly J">J.M. Kelly</name></author><author><name sortKey="Das, P" uniqKey="Das P">P. Das</name></author><author><name sortKey="Tomas, A M" uniqKey="Tomas A">A.M. Tomás</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Krobitsch, S" uniqKey="Krobitsch S">S. Krobitsch</name></author><author><name sortKey="Brandau, S" uniqKey="Brandau S">S. Brandau</name></author><author><name sortKey="Hoyer, C" uniqKey="Hoyer C">C. Hoyer</name></author><author><name sortKey="Schmetz, C" uniqKey="Schmetz C">C. Schmetz</name></author><author><name sortKey="Hubel, A" uniqKey="Hubel A">A. Hübel</name></author><author><name sortKey="Clos, J" uniqKey="Clos J">J. Clos</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Laban, A" uniqKey="Laban A">A. Laban</name></author><author><name sortKey="Wirth, D F" uniqKey="Wirth D">D.F. Wirth</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Legare, D" uniqKey="Legare D">D. Legare</name></author><author><name sortKey="Cayer, S" uniqKey="Cayer S">S. Cayer</name></author><author><name sortKey="Singh, A K" uniqKey="Singh A">A.K. Singh</name></author><author><name sortKey="Richard, D" uniqKey="Richard D">D. Richard</name></author><author><name sortKey="Papadopoulou, B" uniqKey="Papadopoulou B">B. Papadopoulou</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Leprohon, P" uniqKey="Leprohon P">P. Leprohon</name></author><author><name sortKey="Legare, D" uniqKey="Legare D">D. Legare</name></author><author><name sortKey="Raymond, F" uniqKey="Raymond F">F. Raymond</name></author><author><name sortKey="Madore, E" uniqKey="Madore E">E. Madore</name></author><author><name sortKey="Hardiman, G" uniqKey="Hardiman G">G. Hardiman</name></author><author><name sortKey="Corbeil, J" uniqKey="Corbeil J">J. Corbeil</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Llanos Cuentas, A" uniqKey="Llanos Cuentas A">A. Llanos-Cuentas</name></author><author><name sortKey="Tulliano, G" uniqKey="Tulliano G">G. Tulliano</name></author><author><name sortKey="Araujo Castillo, R" uniqKey="Araujo Castillo R">R. Araujo-Castillo</name></author><author><name sortKey="Miranda Verastegui, C" uniqKey="Miranda Verastegui C">C. Miranda-Verastegui</name></author><author><name sortKey="Santamaria Castrellon, G" uniqKey="Santamaria Castrellon G">G. Santamaria-Castrellon</name></author><author><name sortKey="Ramirez, L" uniqKey="Ramirez L">L. Ramirez</name></author><author><name sortKey="Lazo, M" uniqKey="Lazo M">M. Lazo</name></author><author><name sortKey="De Doncker, S" uniqKey="De Doncker S">S. De Doncker</name></author><author><name sortKey="Boelaert, M" uniqKey="Boelaert M">M. Boelaert</name></author><author><name sortKey="Robays, J" uniqKey="Robays J">J. Robays</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author><author><name sortKey="Arevalo, J" uniqKey="Arevalo J">J. Arevalo</name></author><author><name sortKey="Chappuis, F" uniqKey="Chappuis F">F. Chappuis</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Lye, L F" uniqKey="Lye L">L.F. Lye</name></author><author><name sortKey="Owens, K" uniqKey="Owens K">K. Owens</name></author><author><name sortKey="Shi, H" uniqKey="Shi H">H. Shi</name></author><author><name sortKey="Murta, S M" uniqKey="Murta S">S.M. Murta</name></author><author><name sortKey="Vieira, A C" uniqKey="Vieira A">A.C. Vieira</name></author><author><name sortKey="Turco, S J" uniqKey="Turco S">S.J. Turco</name></author><author><name sortKey="Tschudi, C" uniqKey="Tschudi C">C. Tschudi</name></author><author><name sortKey="Ullu, E" uniqKey="Ullu E">E. Ullu</name></author><author><name sortKey="Beverley, S M" uniqKey="Beverley S">S.M. Beverley</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Mann, H B" uniqKey="Mann H">H.B. Mann</name></author><author><name sortKey="Whitney, D R" uniqKey="Whitney D">D.R. Whitney</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Mannaert, A" uniqKey="Mannaert A">A. Mannaert</name></author><author><name sortKey="Downing, T" uniqKey="Downing T">T. Downing</name></author><author><name sortKey="Imamura, H" uniqKey="Imamura H">H. Imamura</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Mookerjee Basu, J" uniqKey="Mookerjee Basu J">J. Mookerjee Basu</name></author><author><name sortKey="Mookerjee, A" uniqKey="Mookerjee A">A. Mookerjee</name></author><author><name sortKey="Banerjee, R" uniqKey="Banerjee R">R. Banerjee</name></author><author><name sortKey="Saha, M" uniqKey="Saha M">M. Saha</name></author><author><name sortKey="Singh, S" uniqKey="Singh S">S. Singh</name></author><author><name sortKey="Naskar, K" uniqKey="Naskar K">K. Naskar</name></author><author><name sortKey="Tripathy, G" uniqKey="Tripathy G">G. Tripathy</name></author><author><name sortKey="Sinha, P K" uniqKey="Sinha P">P.K. Sinha</name></author><author><name sortKey="Pandey, K" uniqKey="Pandey K">K. Pandey</name></author><author><name sortKey="Sundar, S" uniqKey="Sundar S">S. Sundar</name></author><author><name sortKey="Bimal, S" uniqKey="Bimal S">S. Bimal</name></author><author><name sortKey="Das, P K" uniqKey="Das P">P.K. Das</name></author><author><name sortKey="Choudhuri, S K" uniqKey="Choudhuri S">S.K. Choudhuri</name></author><author><name sortKey="Roy, S" uniqKey="Roy S">S. Roy</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Mukherjee, B" uniqKey="Mukherjee B">B. Mukherjee</name></author><author><name sortKey="Mukhopadhyay, R" uniqKey="Mukhopadhyay R">R. Mukhopadhyay</name></author><author><name sortKey="Bannerjee, B" uniqKey="Bannerjee B">B. Bannerjee</name></author><author><name sortKey="Chowdhury, S" uniqKey="Chowdhury S">S. Chowdhury</name></author><author><name sortKey="Mukherjee, S" uniqKey="Mukherjee S">S. Mukherjee</name></author><author><name sortKey="Naskar, K" uniqKey="Naskar K">K. Naskar</name></author><author><name sortKey="Allam, U S" uniqKey="Allam U">U.S. Allam</name></author><author><name sortKey="Chakravortty, D" uniqKey="Chakravortty D">D. Chakravortty</name></author><author><name sortKey="Sundar, S" uniqKey="Sundar S">S. Sundar</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author><author><name sortKey="Roy, S" uniqKey="Roy S">S. Roy</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author><author><name sortKey="Haimeur, A" uniqKey="Haimeur A">A. Haimeur</name></author><author><name sortKey="Grondin, K" uniqKey="Grondin K">K. Grondin</name></author><author><name sortKey="Legare, D" uniqKey="Legare D">D. Legare</name></author><author><name sortKey="Papadopoulou, B" uniqKey="Papadopoulou B">B. Papadopoulou</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author><author><name sortKey="Legare, D" uniqKey="Legare D">D. Legare</name></author><author><name sortKey="Papadopoulou, B" uniqKey="Papadopoulou B">B. Papadopoulou</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Peacock, C S" uniqKey="Peacock C">C.S. Peacock</name></author><author><name sortKey="Seeger, K" uniqKey="Seeger K">K. Seeger</name></author><author><name sortKey="Harris, D" uniqKey="Harris D">D. Harris</name></author><author><name sortKey="Murphy, L" uniqKey="Murphy L">L. Murphy</name></author><author><name sortKey="Ruiz, J C" uniqKey="Ruiz J">J.C. Ruiz</name></author><author><name sortKey="Quail, M A" uniqKey="Quail M">M.A. Quail</name></author><author><name sortKey="Peters, N" uniqKey="Peters N">N. Peters</name></author><author><name sortKey="Adlem, E" uniqKey="Adlem E">E. Adlem</name></author><author><name sortKey="Tivey, A" uniqKey="Tivey A">A. Tivey</name></author><author><name sortKey="Aslett, M" uniqKey="Aslett M">M. Aslett</name></author><author><name sortKey="Kerhornou, A" uniqKey="Kerhornou A">A. Kerhornou</name></author><author><name sortKey="Ivens, A" uniqKey="Ivens A">A. Ivens</name></author><author><name sortKey="Fraser, A" uniqKey="Fraser A">A. Fraser</name></author><author><name sortKey="Rajandream, M A" uniqKey="Rajandream M">M.A. Rajandream</name></author><author><name sortKey="Carver, T" uniqKey="Carver T">T. Carver</name></author><author><name sortKey="Norbertczak, H" uniqKey="Norbertczak H">H. Norbertczak</name></author><author><name sortKey="Chillingworth, T" uniqKey="Chillingworth T">T. Chillingworth</name></author><author><name sortKey="Hance, Z" uniqKey="Hance Z">Z. Hance</name></author><author><name sortKey="Jagels, K" uniqKey="Jagels K">K. Jagels</name></author><author><name sortKey="Moule, S" uniqKey="Moule S">S. Moule</name></author><author><name sortKey="Ormond, D" uniqKey="Ormond D">D. Ormond</name></author><author><name sortKey="Rutter, S" uniqKey="Rutter S">S. Rutter</name></author><author><name sortKey="Squares, R" uniqKey="Squares R">R. Squares</name></author><author><name sortKey="Whitehead, S" uniqKey="Whitehead S">S. Whitehead</name></author><author><name sortKey="Rabbinowitsch, E" uniqKey="Rabbinowitsch E">E. Rabbinowitsch</name></author><author><name sortKey="Arrowsmith, C" uniqKey="Arrowsmith C">C. Arrowsmith</name></author><author><name sortKey="White, B" uniqKey="White B">B. White</name></author><author><name sortKey="Thurston, S" uniqKey="Thurston S">S. Thurston</name></author><author><name sortKey="Bringaud, F" uniqKey="Bringaud F">F. Bringaud</name></author><author><name sortKey="Baldauf, S L" uniqKey="Baldauf S">S.L. Baldauf</name></author><author><name sortKey="Faulconbridge, A" uniqKey="Faulconbridge A">A. Faulconbridge</name></author><author><name sortKey="Jeffares, D" uniqKey="Jeffares D">D. Jeffares</name></author><author><name sortKey="Depledge, D P" uniqKey="Depledge D">D.P. Depledge</name></author><author><name sortKey="Oyola, S O" uniqKey="Oyola S">S.O. Oyola</name></author><author><name sortKey="Hilley, J D" uniqKey="Hilley J">J.D. Hilley</name></author><author><name sortKey="Brito, L O" uniqKey="Brito L">L.O. Brito</name></author><author><name sortKey="Tosi, L R" uniqKey="Tosi L">L.R. Tosi</name></author><author><name sortKey="Barrell, B" uniqKey="Barrell B">B. Barrell</name></author><author><name sortKey="Cruz, A K" uniqKey="Cruz A">A.K. Cruz</name></author><author><name sortKey="Mottram, J C" uniqKey="Mottram J">J.C. Mottram</name></author><author><name sortKey="Smith, D F" uniqKey="Smith D">D.F. Smith</name></author><author><name sortKey="Berriman, M" uniqKey="Berriman M">M. Berriman</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Racoosin, E L" uniqKey="Racoosin E">E.L. Racoosin</name></author><author><name sortKey="Swanson, J A" uniqKey="Swanson J">J.A. Swanson</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Racoosin, E L" uniqKey="Racoosin E">E.L. Racoosin</name></author><author><name sortKey="Beverley, S M" uniqKey="Beverley S">S.M. Beverley</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Reiling, L" uniqKey="Reiling L">L. Reiling</name></author><author><name sortKey="Chrobak, M" uniqKey="Chrobak M">M. Chrobak</name></author><author><name sortKey="Schmetz, C" uniqKey="Schmetz C">C. Schmetz</name></author><author><name sortKey="Clos, J" uniqKey="Clos J">J. Clos</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Rijal, S" uniqKey="Rijal S">S. Rijal</name></author><author><name sortKey="Yardley, V" uniqKey="Yardley V">V. Yardley</name></author><author><name sortKey="Chappuis, F" uniqKey="Chappuis F">F. Chappuis</name></author><author><name sortKey="Decuypere, S" uniqKey="Decuypere S">S. Decuypere</name></author><author><name sortKey="Khanal, B" uniqKey="Khanal B">B. Khanal</name></author><author><name sortKey="Singh, R" uniqKey="Singh R">R. Singh</name></author><author><name sortKey="Boelaert, M" uniqKey="Boelaert M">M. Boelaert</name></author><author><name sortKey="De Doncker, S" uniqKey="De Doncker S">S. De Doncker</name></author><author><name sortKey="Croft, S" uniqKey="Croft S">S. Croft</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Roberts, W L" uniqKey="Roberts W">W.L. Roberts</name></author><author><name sortKey="Berman, J D" uniqKey="Berman J">J.D. Berman</name></author><author><name sortKey="Rainey, P M" uniqKey="Rainey P">P.M. Rainey</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Rogers, M B" uniqKey="Rogers M">M.B. Rogers</name></author><author><name sortKey="Hilley, J D" uniqKey="Hilley J">J.D. Hilley</name></author><author><name sortKey="Dickens, N J" uniqKey="Dickens N">N.J. Dickens</name></author><author><name sortKey="Wilkes, J" uniqKey="Wilkes J">J. Wilkes</name></author><author><name sortKey="Bates, P A" uniqKey="Bates P">P.A. Bates</name></author><author><name sortKey="Depledge, D P" uniqKey="Depledge D">D.P. Depledge</name></author><author><name sortKey="Harris, D" uniqKey="Harris D">D. Harris</name></author><author><name sortKey="Her, Y" uniqKey="Her Y">Y. Her</name></author><author><name sortKey="Herzyk, P" uniqKey="Herzyk P">P. Herzyk</name></author><author><name sortKey="Imamura, H" uniqKey="Imamura H">H. Imamura</name></author><author><name sortKey="Otto, T D" uniqKey="Otto T">T.D. Otto</name></author><author><name sortKey="Sanders, M" uniqKey="Sanders M">M. Sanders</name></author><author><name sortKey="Seeger, K" uniqKey="Seeger K">K. Seeger</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author><author><name sortKey="Berriman, M" uniqKey="Berriman M">M. Berriman</name></author><author><name sortKey="Smith, D F" uniqKey="Smith D">D.F. Smith</name></author><author><name sortKey="Hertz Fowler, C" uniqKey="Hertz Fowler C">C. Hertz-Fowler</name></author><author><name sortKey="Mottram, J C" uniqKey="Mottram J">J.C. Mottram</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Sambrook, J" uniqKey="Sambrook J">J. Sambrook</name></author><author><name sortKey="Russell, D W" uniqKey="Russell D">D.W. Russell</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Sch Fer, C" uniqKey="Sch Fer C">C. Schäfer</name></author><author><name sortKey="Tejera Nevado, P" uniqKey="Tejera Nevado P">P. Tejera Nevado</name></author><author><name sortKey="Zander, D" uniqKey="Zander D">D. Zander</name></author><author><name sortKey="Clos, J" uniqKey="Clos J">J. Clos</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Shaked Mishan, P" uniqKey="Shaked Mishan P">P. Shaked-Mishan</name></author><author><name sortKey="Ulrich, N" uniqKey="Ulrich N">N. Ulrich</name></author><author><name sortKey="Ephros, M" uniqKey="Ephros M">M. Ephros</name></author><author><name sortKey="Zilberstein, D" uniqKey="Zilberstein D">D. Zilberstein</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Soto, J" uniqKey="Soto J">J. Soto</name></author><author><name sortKey="Toledo, J" uniqKey="Toledo J">J. Toledo</name></author><author><name sortKey="Vega, J" uniqKey="Vega J">J. Vega</name></author><author><name sortKey="Berman, J" uniqKey="Berman J">J. Berman</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Sundar, S" uniqKey="Sundar S">S. Sundar</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Tull, D" uniqKey="Tull D">D. Tull</name></author><author><name sortKey="Vince, J E" uniqKey="Vince J">J.E. Vince</name></author><author><name sortKey="Callaghan, J M" uniqKey="Callaghan J">J.M. Callaghan</name></author><author><name sortKey="Naderer, T" uniqKey="Naderer T">T. Naderer</name></author><author><name sortKey="Spurck, T" uniqKey="Spurck T">T. Spurck</name></author><author><name sortKey="Mcfadden, G I" uniqKey="Mcfadden G">G.I. McFadden</name></author><author><name sortKey="Currie, G" uniqKey="Currie G">G. Currie</name></author><author><name sortKey="Ferguson, K" uniqKey="Ferguson K">K. Ferguson</name></author><author><name sortKey="Bacic, A" uniqKey="Bacic A">A. Bacic</name></author><author><name sortKey="Mcconville, M J" uniqKey="Mcconville M">M.J. McConville</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Tull, D" uniqKey="Tull D">D. Tull</name></author><author><name sortKey="Naderer, T" uniqKey="Naderer T">T. Naderer</name></author><author><name sortKey="Spurck, T" uniqKey="Spurck T">T. Spurck</name></author><author><name sortKey="Mertens, H D" uniqKey="Mertens H">H.D. Mertens</name></author><author><name sortKey="Heng, J" uniqKey="Heng J">J. Heng</name></author><author><name sortKey="Mcfadden, G I" uniqKey="Mcfadden G">G.I. McFadden</name></author><author><name sortKey="Gooley, P R" uniqKey="Gooley P">P.R. Gooley</name></author><author><name sortKey="Mcconville, M J" uniqKey="Mcconville M">M.J. McConville</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Tull, D" uniqKey="Tull D">D. Tull</name></author><author><name sortKey="Heng, J" uniqKey="Heng J">J. Heng</name></author><author><name sortKey="Gooley, P R" uniqKey="Gooley P">P.R. Gooley</name></author><author><name sortKey="Naderer, T" uniqKey="Naderer T">T. Naderer</name></author><author><name sortKey="Mcconville, M J" uniqKey="Mcconville M">M.J. McConville</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ubeda, J M" uniqKey="Ubeda J">J.M. Ubeda</name></author><author><name sortKey="Legare, D" uniqKey="Legare D">D. Legare</name></author><author><name sortKey="Raymond, F" uniqKey="Raymond F">F. Raymond</name></author><author><name sortKey="Ouameur, A A" uniqKey="Ouameur A">A.A. Ouameur</name></author><author><name sortKey="Boisvert, S" uniqKey="Boisvert S">S. Boisvert</name></author><author><name sortKey="Rigault, P" uniqKey="Rigault P">P. Rigault</name></author><author><name sortKey="Corbeil, J" uniqKey="Corbeil J">J. Corbeil</name></author><author><name sortKey="Tremblay, M J" uniqKey="Tremblay M">M.J. Tremblay</name></author><author><name sortKey="Olivier, M" uniqKey="Olivier M">M. Olivier</name></author><author><name sortKey="Papadopoulou, B" uniqKey="Papadopoulou B">B. Papadopoulou</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ullu, E" uniqKey="Ullu E">E. Ullu</name></author><author><name sortKey="Tschudi, C" uniqKey="Tschudi C">C. Tschudi</name></author><author><name sortKey="Chakraborty, T" uniqKey="Chakraborty T">T. Chakraborty</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Vergnes, B" uniqKey="Vergnes B">B. Vergnes</name></author><author><name sortKey="Gourbal, B" uniqKey="Gourbal B">B. Gourbal</name></author><author><name sortKey="Girard, I" uniqKey="Girard I">I. Girard</name></author><author><name sortKey="Sundar, S" uniqKey="Sundar S">S. Sundar</name></author><author><name sortKey="Drummelsmith, J" uniqKey="Drummelsmith J">J. Drummelsmith</name></author><author><name sortKey="Ouellette, M" uniqKey="Ouellette M">M. Ouellette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Yardley, V" uniqKey="Yardley V">V. Yardley</name></author><author><name sortKey="Ortuno, N" uniqKey="Ortuno N">N. Ortuno</name></author><author><name sortKey="Llanos Cuentas, A" uniqKey="Llanos Cuentas A">A. Llanos-Cuentas</name></author><author><name sortKey="Chappuis, F" uniqKey="Chappuis F">F. Chappuis</name></author><author><name sortKey="Doncker, S D" uniqKey="Doncker S">S.D. Doncker</name></author><author><name sortKey="Ramirez, L" uniqKey="Ramirez L">L. Ramirez</name></author><author><name sortKey="Croft, S" uniqKey="Croft S">S. Croft</name></author><author><name sortKey="Arevalo, J" uniqKey="Arevalo J">J. Arevalo</name></author><author><name sortKey="Adaui, V" uniqKey="Adaui V">V. Adaui</name></author><author><name sortKey="Bermudez, H" uniqKey="Bermudez H">H. Bermudez</name></author><author><name sortKey="Decuypere, S" uniqKey="Decuypere S">S. Decuypere</name></author><author><name sortKey="Dujardin, J C" uniqKey="Dujardin J">J.C. Dujardin</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Int J Parasitol Drugs Drug Resist</journal-id><journal-id journal-id-type="iso-abbrev">Int J Parasitol Drugs Drug Resist</journal-id><journal-title-group><journal-title>International Journal for Parasitology: Drugs and Drug Resistance</journal-title></journal-title-group><issn pub-type="epub">2211-3207</issn><publisher><publisher-name>Elsevier</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">24596667</article-id><article-id pub-id-type="pmc">3940081</article-id><article-id pub-id-type="publisher-id">S2211-3207(13)00020-1</article-id><article-id pub-id-type="doi">10.1016/j.ijpddr.2013.11.004</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>A novel marker, <italic>ARM58</italic>, confers antimony resistance to <italic>Leishmania</italic> spp.<sup><xref ref-type="fn" rid="d32e504">☆</xref></sup></article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Nühs</surname><given-names>Andrea</given-names></name><xref rid="af005" ref-type="aff">a</xref><xref rid="fn1" ref-type="fn">1</xref></contrib><contrib contrib-type="author"><name><surname>Schäfer</surname><given-names>Carola</given-names></name><xref rid="af005" ref-type="aff">a</xref><xref rid="fn2" ref-type="fn">2</xref></contrib><contrib contrib-type="author"><name><surname>Zander</surname><given-names>Dorothea</given-names></name><xref rid="af005" ref-type="aff">a</xref></contrib><contrib contrib-type="author"><name><surname>Trübe</surname><given-names>Leona</given-names></name><xref rid="af005" ref-type="aff">a</xref><xref rid="fn3" ref-type="fn">3</xref></contrib><contrib contrib-type="author"><name><surname>Tejera Nevado</surname><given-names>Paloma</given-names></name><xref rid="af005" ref-type="aff">a</xref></contrib><contrib contrib-type="author"><name><surname>Schmidt</surname><given-names>Sonja</given-names></name><xref rid="af005" ref-type="aff">a</xref><xref rid="fn4" ref-type="fn">4</xref></contrib><contrib contrib-type="author"><name><surname>Arevalo</surname><given-names>Jorge</given-names></name><xref rid="af010" ref-type="aff">b</xref></contrib><contrib contrib-type="author"><name><surname>Adaui</surname><given-names>Vanessa</given-names></name><xref rid="af010" ref-type="aff">b</xref></contrib><contrib contrib-type="author"><name><surname>Maes</surname><given-names>Louis</given-names></name><xref rid="af020" ref-type="aff">d</xref></contrib><contrib contrib-type="author"><name><surname>Dujardin</surname><given-names>Jean-Claude</given-names></name><xref rid="af015" ref-type="aff">c</xref><xref rid="af020" ref-type="aff">d</xref></contrib><contrib contrib-type="author"><name><surname>Clos</surname><given-names>Joachim</given-names></name><email>clos@bnitm.de</email><xref rid="af005" ref-type="aff">a</xref><xref rid="cor1" ref-type="corresp">⁎</xref></contrib></contrib-group><aff id="af005"><label>a</label>Bernhard Nocht Institute for Tropical Medicine, D20359 Hamburg, Germany</aff><aff id="af010"><label>b</label>Instituto de Medicina Tropical Alexander von Humboldt, Universidad Peruana Cayetano Heredia, Lima, Peru</aff><aff id="af015"><label>c</label>Instituut voor Tropische Geneeskunde, Antwerp, Belgium</aff><aff id="af020"><label>d</label>Department of Biomedical Sciences, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium</aff><author-notes><corresp id="cor1"><label>⁎</label>Corresponding author. Address: Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht St. 74, D20359 Hamburg, Germany. Tel.: +49 40 42818 481; fax: +49 42818 512. <email>clos@bnitm.de</email></corresp><fn id="fn1"><label>1</label><p>Present address: Drug Discovery Unit, Division of Biological Chemistry and Drug Discovery, University of Dundee, Dundee, UK.</p></fn><fn id="fn2"><label>2</label><p>Present address: Heinrich Pette Institute for Experimental Virology, Hamburg, Germany.</p></fn><fn id="fn3"><label>3</label><p>Present address: Institute for Medical Microbiology, Virology and Hygiene, Hamburg, Germany.</p></fn><fn id="fn4"><label>4</label><p>Present address: Euroimmun AG, Division Medical Scientific Information, Lübeck, Germany.</p></fn></author-notes><pub-date pub-type="pmc-release"><day>6</day><month>12</month><year>2013</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was
based on .</pmc-comment>
<pub-date pub-type="epub"><day>6</day><month>12</month><year>2013</year></pub-date><pub-date pub-type="collection"><month>4</month><year>2014</year></pub-date><volume>4</volume><issue>1</issue><fpage>37</fpage><lpage>47</lpage><history><date date-type="received"><day>24</day><month>8</month><year>2013</year></date><date date-type="rev-recd"><day>22</day><month>11</month><year>2013</year></date><date date-type="accepted"><day>25</day><month>11</month><year>2013</year></date></history><permissions><copyright-statement>© 2013 The Authors</copyright-statement><copyright-year>2013</copyright-year><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-nd/3.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p></license></permissions><abstract abstract-type="graphical"><title>Graphical abstract</title><fig id="f0025" position="anchor"><graphic xlink:href="fx1"></graphic></fig></abstract><abstract abstract-type="author-highlights"><title>Highlights</title><p><list list-type="simple"><list-item id="o0005"><label>•</label><p>Functional cloning identifies a <italic>Leishmania</italic>-specific 58 kD antimony resistance marker, ARM58.</p></list-item><list-item id="o0010"><label>•</label><p>ARM58 overexpression confers antimony resistance.</p></list-item><list-item id="o0015"><label>•</label><p>A neighbouring, structurally related gene lacks antimony resistance function.</p></list-item><list-item id="o0020"><label>•</label><p>ARM58 comprises 4 related domains of unknown function, classified as DUF1935.</p></list-item><list-item id="o0025"><label>•</label><p>Cosmid-based functional cloning is feasible in <italic>L. braziliensis</italic> in spite of RNAi.</p></list-item></list></p></abstract><abstract><p>Protozoa of the <italic>Leishmania</italic> genus cause a variety of disease forms that rank at the top of the list of neglected tropical diseases. Anti-leishmanial drugs based on pentavalent antimony have been the mainstay of therapy for over 60 years and resistance against them is increasingly encountered in the field. The biochemical basis for this is poorly understood and likely diverse. No stringent correlation between genetic markers and antimony resistance has so far been shown, prompting us to use a functional cloning approach to identify markers of resistance. Using gene libraries derived from drug-resistant and drug-sensitive <italic>Leishmania braziliensis</italic> clinical isolates in a functional cloning strategy, we repeatedly selected one gene locus located on chromosome 20 whose amplification confers increased antimony (III) resistance <italic>in vitro</italic> to an otherwise sensitive <italic>L. braziliensis</italic> clone. The gene responsible for the effect encodes a previously hypothetical protein that we dubbed LbrARM58. It comprises four repeats of a domain of unknown function, DUF1935, one of them harbouring a potential trans-membrane domain. The gene is so far unique to the <italic>Leishmania</italic> genus, while a structurally related gene without antimony resistance functionality is also found in <italic>Trypanosoma</italic> spp. Overexpression of LbrARM58 also confers antimony resistance to promastigotes and intracellular amastigotes of the related species <italic>Leishmania infantum</italic>, indicating a conserved function in Old World and New World <italic>Leishmania</italic> species. Our results also show that in spite of their RNAi system, <italic>L. braziliensis</italic> promastigotes can serve as acceptor cells for episomally propagated cosmid libraries, at least for the initial stages of functional cloning efforts.</p></abstract><kwd-group><title>Keywords</title><kwd><italic>Leishmania braziliensis</italic></kwd><kwd>Antimony</kwd><kwd>Resistance</kwd></kwd-group></article-meta></front><body><sec sec-type="introduction" id="s0005"><label>1</label><title>Introduction</title><p>Leishmaniasis is a parasitic disease caused by protozoa of the genus <italic>Leishmania</italic> and found on four continents with an estimated annual incidence of between 900,000 and 1.8 million cases (<xref rid="b0020" ref-type="bibr">Alvar et al., 2012</xref>). Leishmaniasis is a poverty related disease with many endemic countries lacking the infrastructure and funds for effective treatment and control measures. The clinical manifestations range from the generalised visceral leishmaniasis (VL) or Kala-Azar, to cutaneous leishmaniasis (CL) and mucocutaneous infections (MCL) and are mostly determined by the infecting <italic>Leishmania</italic> species.</p><p>Therapy against leishmaniasis still relies heavily on two formulations of pentavalent antimony (Sb<sup>V</sup>), meglumine antimoniate (Glucantime®) and sodium stibogluconate (Pentostam®). Developed in the first half of the twentieth century, these compounds are still the mainstay of therapy in most endemic regions. Resistance against Sb<sup>V</sup> has been on the rise since the 1970s. For Indian Kala-azar, the high rate of antimonial treatment failure (>60%) has all but eliminated those cost-effective drugs from the arsenal of clinicians (<xref rid="b0235 b0070" ref-type="bibr">Sundar, 2001; Croft et al., 2006</xref>).</p><p>Pentavalent antimony, Sb<sup>V</sup>, is assumed to be a pro-drug, requiring reduction to Sb<sup>III</sup> either by the parasite or by the host cell. Sb<sup>V</sup> has very little toxicity for promastigotes of <italic>Leishmania donovani</italic>, apparently due to their inability to reduce Sb<sup>V</sup>, whilst amastigotes are susceptible to varying degrees depending on their reducing capacity (<xref rid="b0210 b0225" ref-type="bibr">Roberts et al., 1995; Shaked-Mishan et al., 2001</xref>). In <italic>L. tarentolae</italic>, a non-human pathogenic species, increased levels of trypanothion were found to aid in the detoxification of Sb<sup>III</sup> (<xref rid="b0095" ref-type="bibr">Haimeur et al., 1999</xref>), as did increased levels of P-glycoproteins that act as extrusion pumps for Sb<sup>III</sup> (<xref rid="b0090 b0175" ref-type="bibr">Grondin et al., 1997; Ouellette et al., 1998</xref>). Conversely, the reduction of aquaglyceroporin 1 levels is linked to reduced uptake of Sb<sup>III</sup> and increased resistance in <italic>L. major</italic> (<xref rid="b0085" ref-type="bibr">Gourbal et al., 2004</xref>).</p><p>The diversity of pathways linked to antimony resistance is further compounded by a recent finding that some <italic>L. donovani</italic> isolates from treatment failure cases can induce expression of host cell multi-drug resistance genes (<xref rid="b0165 b0170" ref-type="bibr">Mookerjee Basu et al., 2008; Mukherjee et al., 2013</xref>), thus relying on host cell functions for resistance to therapy.</p><p>Compared with Northern India, treatment failure of antimony-based drugs is less prevalent in South America. One of the chief disease agents in Brazil, <italic>L.</italic> (<italic>Viannia</italic>) <italic>braziliensis</italic>, is known to be sensitive to Sb<sup>V</sup> treatment <italic>in vitro</italic> and responsive in the clinical practice (<xref rid="b0070 b0030" ref-type="bibr">Croft et al., 2006; Azeredo-Coutinho et al., 2007</xref>). Nevertheless, primary antimony therapy has a failure rate of ∼20–25%, depending on the endemic region (<xref rid="b0230 b0025 b0145" ref-type="bibr">Soto et al., 2005; Arevalo et al., 2007; Llanos-Cuentas et al., 2008</xref>), and sensitivity varies between patient isolates, even before the start of the treatment (<xref rid="b0270 b0030" ref-type="bibr">Yardley et al., 2006; Azeredo-Coutinho et al., 2007</xref>). Infection with <italic>L. braziliensis</italic> was associated with the highest antimonial treatment failure rate (30.4%) among Peruvian patients with cutaneous leishmaniasis (<xref rid="b0025" ref-type="bibr">Arevalo et al., 2007</xref>). The correlation of <italic>in vitro</italic> drug susceptibility with therapeutic success is still debated as the evaluation of antimony susceptibility by <italic>in vitro</italic> macrophage-amastigote assays does not necessarily reflect the <italic>in vivo</italic> situation.</p><p>In <italic>L. braziliensis</italic>, natural antimony resistance does not appear to be linked to phylogenetic markers, but emerges independently in different lineages of this species (<xref rid="b0010" ref-type="bibr">Adaui et al., 2011b</xref>). Additional analyses show that expression of known and suspected marker genes for Sb<sup>III</sup>/Sb<sup>V</sup> resistance display isolate-specific fluctuations, possibly representing a great clonal variety (<xref rid="b0005" ref-type="bibr">Adaui et al., 2011a</xref>). Differential gene expression analysis of 13 genes in 21 <italic>L. braziliensis</italic> isolates showed a significant correlation between drug resistance and elevated expression of ornithine carboxylase and trypanothion reductase, but not stringent correlations (<xref rid="b0015" ref-type="bibr">Adaui et al., 2011c</xref>). Therefore, as in <italic>L. donovani</italic>, antimony resistance in <italic>L. braziliensis</italic> is a multi-gene trait resulting from a variety of molecular mechanisms.</p><p>However, there may be more marker genes that are yet unidentified and whose nature may shed light on the pathways leading to drug resistance. A successful strategy employed previously involved the <italic>in vitro</italic> selection for Sb<sup>III</sup> or Sb<sup>V</sup> tolerant parasite populations that were subsequently subjected to an expression analysis for candidate genes. Unanticipated resistance genes cannot be detected in this approach. Likewise, genetic linkage analyses cannot detect random variations of gene expression within populations and isolates. Other, non-hypothesis-driven strategies need to be implemented, such as quantitative genomics and functional cloning.</p><p><italic>Leishmania</italic> parasites are unicellular protozoa of the order Kinetoplastida. Typical of this order is the lack of gene-specific transcription regulation (<xref rid="b0060" ref-type="bibr">Clayton, 2002</xref>), a unique feature among the <italic>Eukaryota</italic>. Most <italic>Leishmania</italic> genes are transcribed as multi-cistronic pre-mRNAs that are subject to subsequent processing through trans-splicing and polyadenylation. Generally, protein coding genes are not interrupted by introns. This fact makes gDNA cosmid libraries the tool of choice for functional cloning in Old World <italic>Leishmania</italic> (<xref rid="b0065" ref-type="bibr">Clos and Choudhury, 2006</xref>). By contrast, the use of selectable episomes is not feasible in the related <italic>Trypanosoma brucei</italic> (<xref rid="b0055" ref-type="bibr">Clayton, 1999</xref>), possibly due to the existence of an RNA silencing system (<xref rid="b0260" ref-type="bibr">Ullu et al., 2004</xref>). Recent evidence indicates that <italic>L.</italic> (<italic>Viannia</italic>) <italic>braziliensis</italic> also possesses the genes encoding key proteins of RNA silencing (<xref rid="b0185" ref-type="bibr">Peacock et al., 2007</xref>), and is susceptible to RNA interference (<xref rid="b0150" ref-type="bibr">Lye et al., 2010</xref>). This was unknown at the onset of our study.</p><p>We have recently used a functional cloning strategy (<xref rid="b0065" ref-type="bibr">Clos and Choudhury, 2006</xref>) to search for genetic markers of drug resistance in <italic>Leishmania infantum</italic>. Promastigotes were transfected with a shuttle cosmid library of <italic>L. infantum</italic> genomic DNA and challenged with the antileishmanial drug, Miltefosine. The two cosmids selected overlapped in a single gene which was shown subsequently to confer increased Miltefosine and Sb<sup>III</sup> resistance upon overexpression (<xref rid="b0050" ref-type="bibr">Choudhury et al., 2008</xref>).</p><p>Expanding on the same strategy, we attempted to identify genes that may differ between antimony resistant and antimony sensitive <italic>Leishmania</italic> clinical isolates. Antimony resistance might arise in a stepwise manner, first to Sb<sup>V</sup> and then to Sb<sup>III</sup> (<xref rid="b0270 b0205" ref-type="bibr">Yardley et al., 2006; Rijal et al., 2007</xref>). This is supported by our observation of three combinations of <italic>in vitro</italic> antimony susceptibility phenotypes among field isolates: (i) parasites sensitive or (ii) tolerant to both Sb<sup>V</sup> and Sb<sup>III</sup>, and (iii) parasites tolerant to Sb<sup>V</sup> only (the majority) (<xref rid="b0270 b0205" ref-type="bibr">Yardley et al., 2006; Rijal et al., 2007</xref>). In this study, we used the Sb<sup>III</sup>- and Sb<sup>V</sup>-resistant isolate MHOM/PE/02/PER104 of <italic>L. braziliensis</italic> (<xref rid="b0270 b0005" ref-type="bibr">Yardley et al., 2006; Adaui et al., 2011a</xref>) as donor for a genomic DNA cosmid library, to transfect Sb<sup>III</sup> s/Sb<sup>V</sup> r clones of isolate MHOM/PE/01/PER002 and to challenge the recombinant population with antimonyl tartrate (Sb<sup>III</sup>). Five independent screens using two libraries from resistant and sensitive isolates, combined with two <italic>L. braziliensis</italic> clones and one <italic>L. peruviana</italic> acceptor strain, yielded three cosmids that overlapped in the same region of the <italic>L. braziliensis</italic> chromosome 20. The region harbours a gene, LbrM20.0210, which upon overexpression in <italic>L. infantum</italic> increases the IC<sub>50</sub> for Sb<sup>III</sup> up to threefold and increases parasite survival inside macrophages under Sb<sup>V</sup> pressure.</p></sec><sec sec-type="materials|methods" id="s0010"><label>2</label><title>Materials and methods</title><sec id="s0015"><label>2.1</label><title>Parasite strains and isolates</title><p><italic>L. braziliensis</italic> isolates MHOM/PE/2002/PER104 (PER104) and MHOM/PE/2001/PER002 (PER002) have been described (<xref rid="b0230 b0145" ref-type="bibr">Soto et al., 2005; Llanos-Cuentas et al., 2008</xref>). Of the latter, two clones were isolated with confirmed Sb<sup>III</sup> s/Sb<sup>V</sup> r phenotype. <italic>L. peruviana</italic> strain MHOM/PE/??/ LC2434, clone 5, was a gift from Lenea Campino, Lisbon. <italic>L. infantum</italic> strain MHOM/FR/91/LEM2259 was described (<xref rid="b0075 b0050" ref-type="bibr">Garin et al., 2001; Choudhury et al., 2008</xref>).</p></sec><sec id="s0020"><label>2.2</label><title>Parasite cultivation and selection procedures</title><p>Promastigotes were cultivated at 25 °C, pH 7.0 in Locke’s Solution (0.8% NaCl; 0.02% KCl; 0.03% KH<sub>2</sub>PO<sub>4</sub>; 0.01% MgSO<sub>4</sub> × 7H<sub>2</sub>O; 0.1% NaHCO<sub>3</sub>; 0.25% glucose; all w/v) over Tobie’s blood agar (20% rabbit blood, defibrinated; 1.5% agar; 1.5% Bacto-Tryptose; 0.4% NaCl; 0.04% KCl; 0.5% Na<sub>3</sub>PO<sub>4</sub> × 12H<sub>2</sub>O) and with 1% <sc>l</sc>-glutamine/Penicillin/Streptomycin (Sigma–Aldrich #D3462). G418 (Geneticin sulfate, Carl Roth) was added to 12 μg ml<sup>−1</sup> for recombinant cell populations. Cell density was determined using Neubauer chambers with 0.025 mm width.</p><p>Alternatively, <italic>L. braziliensis</italic> and <italic>L. peruviana</italic> were cultivated at 25 °C, pH 7.0 in Schneider’s Insect Medium supplemented with 10% (v/v) heat-inactivated fetal calf serum, 2% (v/v) sterile filtered human urine, 0.04% (w/v) NaHCO<sub>3</sub>, 0.079% (w/v) CaCl<sub>2</sub> × 2H<sub>2</sub>O, and 25 μg ml<sup>-1</sup> gentamycin. <italic>L. infantum</italic> was cultivated in supplemented Medium 199 (<xref rid="b0125" ref-type="bibr">Krobitsch et al., 1998</xref>). G418 was added to 50 μg ml<sup>−1</sup> for recombinant cell populations. Cell density was monitored using a Schaerfe System CASY® cell counter. For growth experiments, promastigotes were seeded at 5 × 10<sup>5</sup> cells ml<sup>−1</sup> in modified M199 without G418 and cell density was monitored for 3 days.</p></sec><sec id="s0025"><label>2.3</label><title><italic>In vitro</italic> infection</title><p><italic>In vitro</italic> infections were performed as described (<xref rid="b0200" ref-type="bibr">Reiling et al., 2010</xref>). Bone marrow-derived macrophages (BMMs) were isolated from femurs of C57BL/6 mice and incubated in Iscove‘s Modified Dulbecco‘s Medium (IMDM) supplemented with 10% heat inactivated FCS, 5% horse serum, and 30% L929 cell supernatant containing macrophage colony-stimulating factor (MCSF), modified after (<xref rid="b0195" ref-type="bibr">Racoosin and Swanson, 1989</xref>). After differentiation, BMMs were harvested, washed, and seeded into 8-well chamber slides (Nunc) at a density of 4 × 10<sup>5</sup> cells/well. Macrophages were incubated for 48 h at 37 °C and 9% CO<sub>2</sub> to permit adhesion. BMMs were then infected using stationary phase promastigotes (<xref rid="b0190" ref-type="bibr">Racoosin and Beverley, 1997</xref>) at 10 parasites per macrophage. After 4 h of incubation at 37 °C in modified Medium 199 (<xref rid="b0125" ref-type="bibr">Krobitsch et al., 1998</xref>), free parasites were washed off with PBS. Incubation was continued for another 72 h in IMDM without or with 160 μg ml<sup>-1</sup> of Pentostam® at 37 °C and 9% CO<sub>2</sub>. The medium was removed. The cells were washed twice in PBS and subsequently fixed in ice-cold methanol. Infection rates were assessed by nuclear staining with DAPI (1.25 μg ml<sup>−1</sup>, Sigma) and fluorescence microscopy. Pentostam® (formulated for clinical use, GlaxoSmithKline) was a gift from the Bundeswehr Krankenhaus Hamburg, Tropical Medicine Unit.</p></sec><sec id="s0030"><label>2.4</label><title>Genomic DNA preparation and cosmid library construction</title><p>Construction of a <italic>Leishmania</italic> genomic DNA cosmid library in the vector pcosTL (<xref rid="b0120" ref-type="bibr">Kelly et al., 1994</xref>) has been described (<xref rid="b0110" ref-type="bibr">Hoyer et al., 2001</xref>). Briefly, cosmid libraries of <italic>L. braziliensis</italic> strains PER104 and PER002 (<xref rid="b0270 b0010" ref-type="bibr">Yardley et al., 2006; Adaui et al., 2011b</xref>) were prepared by cleavage of the shuttle cosmid vector pcosTL with <italic>Sma</italic>I and <italic>Bam</italic>HI and ligation with size-selected <italic>Sau</italic>3AI partial digest products of genomic DNA prepared by glass rod spooling from an ethanol precipitation (<xref rid="b0220" ref-type="bibr">Sambrook and Russell, 2001</xref>). After packaging using the Gigapack Gold II kit (Stratagene), the complexities of the libraries were tested, after which the libraries were amplified and stored at −70 °C.</p></sec><sec id="s0035"><label>2.5</label><title>Electroporation, selection, and recovery of cosmid DNA</title><p>Electrotransfection of <italic>Leishmania</italic> promastigotes was carried out as described (<xref rid="b0125" ref-type="bibr">Krobitsch et al., 1998</xref>). Promastigotes were harvested during late log phase of growth, washed twice in ice–cold PBS, once in pre-chilled electroporation buffer and suspended at a density of 1 × 10<sup>8</sup> ml<sup>−1</sup> in electroporation buffer (<xref rid="b0130 b0115" ref-type="bibr">Laban and Wirth, 1989; Kapler et al., 1990</xref>). 50 μg of circular DNA in an electroporation cuvette was mixed on ice with 0.4 ml of the cell suspension. The mixture was immediately subjected to electroporation using a Bio-Rad Gene Pulser apparatus. Electrotransfection of DNA was carried out by three pulses at 2.750 V/cm and 25 μF in a 4 mm electroporation cuvette. Mock transfection was performed in identical fashion, however without plasmid or cosmid DNA, to obtain negative control strains for antibiotic selection. Following electroporation, cells were kept on ice for 10 min before they were transferred to 10 ml drug-free medium. G418 (12–50 μg ml<sup>−1</sup>) was added after 24 h for selection of recombinant cells.</p><p>Dose-inhibition curves for antimonyl tartrate (Sigma–Aldrich #383376) were established by seeding the promastigotes at 5 × 10<sup>5</sup> ml<sup>−1</sup> in medium containing various concentrations of a drug, but lacking the selection antibiotic G418. For primary screens, the selection was performed in the presence of G418, to select against spontaneous drug resistance.</p><p>Recombinant populations of promastigotes transfected either with cosmid library DNA or with the unmodified vector, pcosTL, were seeded in G418-containing medium with Sb<sup>III</sup> at a concentration that inhibits >95% of the growth. This was determined empirically for each batch of antimonyl tartrate and parasite strain. When a cell density of 1 × 10<sup>7</sup> cells ml<sup>−1</sup> was reached, the cells were suspended in fresh medium containing the drug. Cultivation was continued for several days. Conditions were deemed stringent if the control population transfected with the vector pcosTL did not show growth. Surviving parasites were harvested for cosmid isolation.</p><p>Cosmid DNA was prepared from <italic>Leishmania</italic> promastigotes by alkaline lysis, following the protocol for plasmid DNA mini-preparation (<xref rid="b0220" ref-type="bibr">Sambrook and Russell, 2001</xref>). After phenol/chloroform/isoamylalcohol (25:24:1) extraction, cosmid DNA was precipitated by adding 0.7 vol. 2-propanol, washed once with 70% ethanol and dissolved in Tris/EDTA (pH 8.0) buffer.</p></sec><sec id="s0040"><label>2.6</label><title>Cosmid characterisation</title><p>Approximately 100 ng of cosmid DNA was mixed on ice with Library Efficiency DH5α Competent Cells (Invitrogen). Transfection was performed following the manufacturer’s protocol, and recombinant bacteria were plated on LB agar under ampicillin selection.</p><p>Cosmid DNA mini-preparations were performed from ⩾50 individual colonies, and the isolated cosmid DNA was subjected to analytical digest with the restriction enzymes <italic>Eco</italic>RV and <italic>Xba</italic>I. The pattern of restriction fragments was analysed by field inversion gel electrophoresis (<xref rid="b0200" ref-type="bibr">Reiling et al., 2010</xref>).</p></sec><sec id="s0045"><label>2.7</label><title>Construction of cosmid derivates</title><p>The cosmid pcosC1.6 was cut with <italic>Afl</italic>II and re-ligated to create derivative (a). Digest with <italic>Bam</italic>HI and subsequent re-ligation yielded construct (b). A combined digest with <italic>Nde</italic>I and <italic>Bam</italic>HI followed by Klenow enzyme fill-in reaction and ligation yielded construct (c). Excising the <italic>Xba</italic>I fragment and fusing it into the <italic>Xba</italic>I site of pcosTL resulted in construct (d). To produce construct (e), pcosC1.6 was digested with <italic>Xba</italic>I and <italic>Spe</italic>I, and the resulting 5200 bp fragment was ligated into <italic>Xba</italic>I-opened pcosTL vector. Using <italic>Bcl</italic>I instead of <italic>Spe</italic>I in the second step produced construct (210), while cutting construct (e) with <italic>Xba</italic>I and <italic>Bcl</italic>I followed by Klenow enzyme treatment and ligation resulted in construct (220). Schematic representations can be found in <xref rid="f0005" ref-type="fig">Fig. 1</xref>C and in <xref rid="s0140" ref-type="sec">Supplementary data 2.</xref></p></sec><sec id="s0050"><label>2.8</label><title>cDNA synthesis and qPCR</title><p>Real-time qPCR was performed essentially as described (<xref rid="b0050" ref-type="bibr">Choudhury et al., 2008</xref>). Gene-specific primers were 20.0210.F2 (5′-TGATGATGAAGGTGACCGTGACG-3′) and 20.0210.B3 (5′-AAGGAGGGTGTAGACGACGCTCTC-3′). LbrM20.0210 mRNA abundance was calculated relative to the actin signal.</p></sec><sec id="s0055"><label>2.9</label><title><italic>In silico</italic> DNA analysis and data handling</title><p>Significance was assessed by the Mann–Whitney <italic>U</italic>-test (<xref rid="b0155" ref-type="bibr">Mann and Whitney, 1947</xref>). All statistical analyses were performed using the Prism Software (GraphPad). Sequencing was performed by a commercial provider (AGOWA, Berlin). We used the MacVector™ suite software (Versions 10.5–12.7) for <italic>in silico</italic> sequence analysis. BLAST searches were performed at standard settings, using the TriTryp web site (<ext-link ext-link-type="uri" xlink:href="http://tritrypdb.org/tritrypdb//" id="ir0005">http://tritrypdb.org/tritrypdb//</ext-link>). Open reading frames were identified both by onsite analysis, using MacVector™, and by mining of the TriTryp Genome Databases. Sequence alignments were done in ClustalW using the MUSCLE algorithm included with the MacVector® software package. Transmembrane domain predictions were performed at the TMpred website (<ext-link ext-link-type="uri" xlink:href="http://www.ch.embnet.org/software/TMPRED_form.html" id="ir0010">http://www.ch.embnet.org/software/TMPRED_form.html</ext-link>) (<xref rid="b0105" ref-type="bibr">Hofmann and Stoffel, 1993</xref>). Figures were compiled using the Intaglio® vector graphics software.</p></sec><sec id="s0060"><label>2.10</label><title>Animal ethics</title><p>The isolation of bone marrow-derived macrophages from sacrificed mice was done in accordance with the German animal protection laws and regulations.</p></sec></sec><sec sec-type="results" id="s0065"><label>3</label><title>Results</title><sec id="s0070"><label>3.1</label><title>Library construction and transfection</title><p>The genomic DNA from two <italic>L. braziliensis</italic> isolates, the Sb<sup>III</sup> resistant MHOM/PE/02/PER104 (PER104) and the Sb<sup>III</sup> sensitive MHOM/PE/01/PER002 (PER002), were used for construction of two cosmid libraries, pcos104 and pcos002 respectively. The cosmid library DNAs were then used for stable transfection of <italic>L. braziliensis</italic> PER002, clone 7, promastigotes. In addition, the cosmid library pcos104 was electro-transfected into <italic>L. peruviana</italic> promastigotes, to test whether the outcome of the screen was influenced by the acceptor species. The number of recombinant parasites per electroporation reaction was determined by limiting dilution analysis (not shown). Results varied between 960 and 1900 clones per reaction. We therefore pooled 6 electroporation reactions for each library to ensure the necessary number of >4200 clones, that is needed to cover the <italic>L. braziliensis</italic> genome with a confidence of >99%.</p></sec><sec id="s0075"><label>3.2</label><title>First selection (S1) of PER002cl7 parasites bearing the pcos104 library</title><p>First, we established the sensitivity of PER002 promastigotes against Sb<sup>III</sup> in biphasic medium. Dose-inhibition curves suggested that growth of a control strain bearing the empty cosmid vector, PER002 [pcosTL], was reduced by >95% at 90 μM antimonyl tartrate (data not shown). We decided to perform selections at two concentrations, 25 and 90 μM.</p><p>We next selected the cosmid library from the Sb<sup>III</sup> resistant isolate PER104 in the Sb<sup>III</sup> sensitive PER002 background. PER002cl7[pcos104] promastigotes were seeded <italic>in vitro</italic> at 1 × 10<sup>7</sup> cells ml<sup>−1</sup> in biphasic medium and challenged with antimonyl tartrate. PER002cl7[pcosTL] controls were cultivated in parallel. The challenge was maintained for up to 33 days, or until the library-transfected populations showed significant growth. In total, three selections (S1.1–S1.3) were performed, one (S1.1) at 25 μM and two (S1.2 and S1.3) at 90 μM Sb<sup>III</sup>.</p><p>The cosmid DNA from the surviving parasite populations was isolated and then used for transformation of competent <italic>Escherichia coli</italic> DH5α cells. The cosmid DNA from ⩾50 resulting <italic>E. coli</italic> clones was isolated and subjected to restriction fragment length analysis (RFLA) (<xref rid="s0140" ref-type="sec">Supplementary data 1</xref>). One cosmid, designated pcosC1.6, was dominant in all three selections (<xref rid="t0005" ref-type="table">Table 1</xref>). In selection S1 under low antimony pressure (25 μM Sb<sup>III</sup>), pcosC1.6 was identified in 66% of the bacterial clones. In selections S1.2 and S1.3 (both at 90 μM Sb<sup>III</sup>), the same cosmid was recovered from 90% to 98% respectively of the analysed clones. Another cosmid that appeared frequently turned out to be a plasmid contamination, likely contracted during <italic>E. coli</italic> transformation (<xref rid="s0140" ref-type="sec">Supplementary data 1</xref>). The fact that only one cosmid species was recovered after 90 μM Sb<sup>III</sup> selection experiments implicates a strong selective pressure towards a/the gene/s harboured in cosmid pcosC1.6.</p><p>Partial 5′- and 3′ sequence analysis of the genomic DNA insert of pcosC1.6 was performed and used for an alignment with the <italic>L. braziliensis</italic> genome project. The region bracketed by the partial sequences contained two large gaps. Using a primer walking strategy, we filled those sequence gaps to obtain a complete sequence of the pcosC1.6 insert (<xref rid="s0140" ref-type="sec">Supplementary data 3</xref>). Alignment of the complete insert sequence with the <italic>L. braziliensis</italic> chromosome 20 (CHR20) sequence (as of Sep 20, 2013) results in a split alignment (<xref rid="f0005" ref-type="fig">Fig. 1</xref>A). The 5′ ∼15 kb align in reverse complimentary direction to the telomere end of CHR20 (positions ∼50–14,000) whilst the 3′ 24 kb of the cosmid insert align in colinear fashion to CHR20 sequences between positions 56,000 and 80,000. This can be either due to a ligation artefact during library construction joining two smaller DNA fragments or to a faulty contig building for CHR20. The cosmid insert thus comprises 39 kb of genomic DNA and includes eleven complete and one partial open reading frames (<xref rid="f0005" ref-type="fig">Fig. 1</xref>B, <xref rid="s0140" ref-type="sec">Supplementary data 2</xref>).</p></sec><sec id="s0080"><label>3.3</label><title>Quantification of the effect by pcosC1.6</title><p>To quantify the effect of the pcosC1.6 episomes, we performed a dose-inhibition experiment. The Sb<sup>III</sup> susceptibilities of acceptor and library donor parasites, PER002cl7 and PER104, are different. We found PER104 (<xref rid="f0010" ref-type="fig">Fig. 2</xref>A, full circles) to have a >2-fold higher IC<sub>50</sub> (50%-inhibitory concentration) than PER002cl7 (<xref rid="f0010" ref-type="fig">Fig. 2</xref>A, open circles). The vector control strain PER002cl7[pcosTL] showed an IC<sub>50</sub> of 7 μM antimonyl tartrate, whilst the PER002cl7[pcosC1.6] parasites displayed an IC<sub>50</sub> of 16 μM. This 2.3-fold difference caused by the pcosC1.6 transgene is therefore measurable, reproducible (<italic>n</italic> = 5, <italic>p</italic> = 0.002) and in the range of the donor strain PER104.</p></sec><sec id="s0085"><label>3.4</label><title>Second selection (S2) of PER002cl7 parasites bearing the pcos002 library</title><p>The Sb<sup>III</sup> resistance conferred by pcosC1.6 may be caused by a sequence variation in the responsible gene or by the overexpression from an episome. To distinguish between these possibilities, we also performed a selection using the recombinant population PER002cl7[pcos002]. This was designed to identify gene(s) that induce Sb<sup>III</sup> resistance by gene over-expression only, as donor and acceptor strain gDNAs are identical. The parasites were seeded in supplemented Schneider‘s insect medium at 5 × 10<sup>5</sup> cells ml<sup>−1</sup> and challenged with 75 μM Sb<sup>III</sup>, the empirically determined IC<sub>95</sub> (95%-inhibitory concentration) for that batch of antimonyl tartrate. After 17 days of selection, cosmid DNA was isolated from the surviving, recombinant parasites. Competent <italic>E. coli</italic> XL1-blue cells were transformed with the recovered cosmid DNA. RFLA was performed for 100 bacterial clones (data not shown). Five cosmid species (pcosA1-5) were detected after the initial screen (S2.1). Parasites bearing the cosmids pcosA1-5 at equal ratios were then subjected to a second screen (S2.2) under the same conditions. After the secondary selection, 96% of the recovered cosmids corresponded to pcosA3.</p><p>Cosmid pcosA3, like pcosC1.6, contains genomic DNA derived from chromosome 20 and overlaps the genomic DNA insert of pcosC1.6 (<xref rid="f0005" ref-type="fig">Fig. 1</xref>B). This indicates that a quantitative effect is underlying the increased Sb<sup>III</sup> tolerance, meaning that both pcosA3 and pcosC1.6 act through an increase of the relevant gene copy number(s).</p></sec><sec id="s0090"><label>3.5</label><title>Third selection (S3) of <italic>L. peruviana</italic> parasites bearing the pcos104 library</title><p>To test whether the closely related <italic>L. peruviana</italic> yields a similar selection result, a recombinant population of <italic>L. peruviana</italic> [pcos104] was cultivated <italic>in vitro</italic> in supplemented Schneider‘s insect medium and then seeded at 1 × 10<sup>5</sup> cells ml<sup>−1</sup> under a challenge of 15 μM Sb<sup>III</sup>, due to that species’s much lower tolerance for antimonyl tartrate. After 30 days of <italic>in vitro</italic> cultivation, cosmid DNA was isolated from the selected population and transformed into competent <italic>E. coli</italic> XL1-blue cells. RFLA of 50 bacterial clones was performed (data not shown), and a dominant cosmid, pcosB1 was recovered from 40% of the bacterial clones.</p><p>Again, the selected cosmid, pcosB1, corresponds to sequences on chromosome 20 and overlaps the inserts of both pcosC1.6 and pcosA3 (<xref rid="t0005" ref-type="table">Table 1</xref>, <xref rid="f0005" ref-type="fig">Fig. 1</xref>B). Thus, five independent <italic>in vitro</italic> selections under antimonyl tartrate implicate the same genomic region on chromosome 20. The gene(s) responsible for the selective advantage must therefore code for (a) dominant, dose-dependent resistance marker(s) located there.</p><p>Furthermore, the isolation of 3 different cosmids with synthenic gene arrays covering essentially the same region on CHR20 argues against ligation artefacts as the basis for the split sequence alignment between cosmid inserts and the current CHR20 sequence.</p></sec><sec id="s0095"><label>3.6</label><title>Functional deletion analysis of pcosC1.6</title><p>To identify the candidate gene(s) responsible for Sb<sup>III</sup>-resistance, the cosmid pcosC1.6 was truncated by digestion with different restriction enzymes and subsequent re-ligation, resulting in seven constructs that represent different regions of pcosC1.6 (<xref rid="f0005" ref-type="fig">Fig. 1</xref>C). These constructs were then transfected into <italic>L. braziliensis</italic> PER002 clone 7. The recombinant strains were then mixed and selected under Sb<sup>III</sup>. We could not observe the selection of specific truncated pcosC1.6 derivates in those selections, and dose-inhibition experiments for selected transgenic parasite strains were also inconclusive (data not shown).</p><p>At that time, studies of the <italic>L. braziliensis</italic> genome revealed that the components of RNA interference (RNAi) pathways exist in the subgenus <italic>Viannia</italic> (<xref rid="b0185" ref-type="bibr">Peacock et al., 2007</xref>) and that gene regulation due to homologous dsRNA may occur. This was since confirmed (<xref rid="b0150" ref-type="bibr">Lye et al., 2010</xref>). This led us to suspect that dsRNA may interfere with the overexpression from the truncated cosmid episomes. Our constructs and experimental set-up did not allow for an analysis of dsRNA-mediated RNA breakdown by qPCR. Nevertheless, we decided to test the constructs in another species known for the absence of RNAi (<xref rid="b0035" ref-type="bibr">Beverley, 2003</xref>).</p></sec><sec id="s0100"><label>3.7</label><title>Selection for the resistance-mediating gene using <italic>L. infantum</italic> as acceptor species</title><p>We decided to use the Old World <italic>Leishmania</italic> species, <italic>L. infantum</italic>, which lacks genes for key components of the RNAi machinery, such as Argonaute and Dicer, and for which we had experience regarding experimental Sb<sup>III</sup> resistance (<xref rid="b0050" ref-type="bibr">Choudhury et al., 2008</xref>). First, we confirmed that the <italic>L. braziliensis</italic>-derived cosmid pcosC1.6 conferred elevated IC<sub>50</sub> for Sb<sup>III</sup> to <italic>L. infantum</italic>. We performed dose-inhibition growth experiments with <italic>L. infantum</italic> bearing either the empty vector, pcosTL, or the selected cosmid pcosC1.6. Indeed, the IC<sub>50</sub> of <italic>L. infantum</italic> [pcosC1.6] was approximately twice that of <italic>L. infantum</italic> [pcosTL] (<xref rid="f0010" ref-type="fig">Fig. 2</xref>B).</p><p>We next performed two independent Sb<sup>III</sup> screens with <italic>L. infantum</italic> strains bearing the cosmid pcosC1.6 and its truncated derivatives (<xref rid="f0005" ref-type="fig">Fig. 1</xref>C) and mixed at equal ratios (culture C<sub>0</sub>). We seeded two cultures each at 4 × 10<sup>4</sup> cells ml<sup>−1</sup> and selected them either for 12 days at 500 μM Sb<sup>III</sup> (S<sub>12</sub>) or for 21 days at 400 μM Sb<sup>III</sup> (S<sub>21</sub>) μM Sb<sup>III</sup>. Two groups (C<sub>12</sub> and C<sub>21</sub>) were also cultivated for 12 and 21 days respectively, but without antimony pressure. After 12 days (C<sub>12</sub> and S<sub>12</sub>) or 21 days (C<sub>21</sub> and S<sub>21</sub>) of <italic>in vitro</italic> cultivation, cosmid DNA was isolated from the resulting populations. <italic>E. coli</italic> XL1-blue cells were transformed with the re-isolated cosmids. The cosmids from 50 bacterial clones for each selection or control culture were prepared, and RFLA was performed on them to determine the prevalence of truncated derivatives of pcosC1.6.</p><p>Cosmid pcos-210, harbouring only the gene LbrM20.0210, was the most dominant of the recovered transgenes and recovered from 82% (S<sub>12</sub>) to 57% (S<sub>21</sub>) respectively of the bacterial clones (<xref rid="f0005" ref-type="fig">Fig. 1</xref>D). Constructs (a and e), both also harbouring LbrM20.0210, were recovered at lesser rates. This means that 92% (S<sub>12</sub>) and 86% (S<sub>21</sub>) of the re-isolated constructs carry the LbrM20.0210 gene. Since the recovery rates for these cosmids from the non-selected populations were ⩽10%, the cause for LbrM20.0210 selection must be an <italic>in vitro</italic> Sb<sup>III</sup> resistance mediated by this gene.</p></sec><sec id="s0105"><label>3.8</label><title>Analysis of the <italic>L. braziliensis</italic> resistance gene in <italic>L. infantum</italic></title><p>The effect of LbrM20.0210 was further verified and quantified by performing individual Sb<sup>III</sup> dose-inhibition experiments for <italic>L. infantum</italic> carrying the constructs pcosTL (vector control), pcos210 (suspected resistance gene), and pcos-220 (negative control). While Lin[pcosTL] and Lin[pcos-220] show indistinguishable dose-inhibition curves (<xref rid="f0010" ref-type="fig">Fig. 2</xref>C), Lin[pcos-210] increases the IC<sub>50</sub> for Sb<sup>III</sup> 2.3-fold.</p><p>We also confirmed the expression of LbrM20.0210 in <italic>L. infantum</italic> transfected with pcosC1.6 and with pcos-210, using real-time qPCR (<xref rid="f0010" ref-type="fig">Fig. 2</xref>D). Expression was ∼3-fold higher from the pcos-210 construct compared to the original cosmid, pcosC1.6. As expected, <italic>L. infantum</italic> controls did not express the <italic>L. braziliensis</italic> gene. This result explains the preferential selection of pcos-210 over pcosC1.6 as shown in <xref rid="f0005" ref-type="fig">Fig. 1</xref>D. To determine the general level of overexpression from pcosC1.6 over the <italic>L. braziliensis</italic> wild type PER002cl7, we performed another qPCR with cDNA derived from PER002[pcosTL] and PER002[pcosC1.6]. <xref rid="f0010" ref-type="fig">Fig. 2</xref>E shows the result. The pcosC1.6 transgene gives rise to a 5.5-fold elevated LbrM20.0210 RNA level. Although not directly applicable to the <italic>L. infantum</italic> system, this indicates a sizeable overexpression of LbrM20.0210 in the recombinant parasites.</p></sec><sec id="s0110"><label>3.9</label><title>Overexpression of LbrM20.0210 protects intracellular amastigotes against antimony (V)</title><p>Antimony (V) is reduced to antimony (III) in <italic>Leishmania</italic> amastigotes and in macrophages, with the trivalent form being the cytotoxic principle. Sb<sup>III</sup> resistant strains are usually Sb<sup>V</sup>-resistant, but not necessarily vice versa. Therefore, we next tested whether overexpression of <italic>LbrM20.0210</italic> also protects the relevant life cycle stage, intracellular amastigotes, against an Sb<sup>V</sup>-based drug formulation, namely Pentostam®.</p><p><italic>L. infantum</italic> promastigotes transfected either with the vector pcosTL or with pcos210 were grown to stationary phase <italic>in vitro</italic> and used to infect bone marrow-derived murine macrophages <italic>in vitro</italic>. After 4 h, the free parasites were removed and the infected cells were overlayered with medium without or with 160 μg ml<sup>−1</sup> Sb<sup>V</sup>. <xref rid="f0015" ref-type="fig">Fig. 3</xref>A shows the accumulated results from 4 separate infection experiments. In the absence of Sb<sup>V</sup>, the infection rates of <italic>L. infantum</italic> [pcosTL] and <italic>L. infantum</italic> [pcos-210] show only insignificant variation. Under Sb<sup>V</sup> treatment of infected macrophages we observe significant (<italic>p</italic> = 0.029) differences. While <italic>L. infantum</italic> [pcosTL] infection rates drop by 90%, the effect on the <italic>L. infantum</italic> [pcos-210] parasites is less severe. This indicates that LbrM20.0210 can partially protect intracellular amastigotes of <italic>L. infantum</italic> against the effect of an Sb<sup>V</sup>-containing drug. We therefore assigned the moniker <italic>ARM58</italic> (antimony resistance marker of 58 kDa) to <italic>LbrM20.0210</italic> and its product.</p></sec><sec id="s0115"><label>3.10</label><title><italic>ARM58</italic> in Sb resistant and sensitive isolates</title><p>To assess whether ARM58 gene copy number and/or RNA abundance vary between strains, we performed a comparative qPCR analysis to quantify ARM58 RNA in <italic>L. braziliensis</italic> strains PER002 (Sb<sup>III</sup>-sensitive acceptor strain in this study) and PER104 (natural Sb<sup>III</sup>-resistant donor strain for gDNA library). At least based on the qPCR results (<xref rid="f0015" ref-type="fig">Fig. 3</xref>B), we cannot detect variations in ARM58 mRNA levels in the two isolates. Since the strains show different Sb<sup>III</sup> sensitivities <italic>in vitro</italic>, we can exclude variant mRNA levels as cause.</p><p>We also assessed the stability of ARM58 overexpression under different conditions. <italic>L. brasiliensis</italic> PER002[pcos-210] were kept without selection, under G418 (50 μg ml<sup>−1</sup>), or under Sb<sup>III</sup> (3 or 10 μM) for 4 weeks, with twice weekly medium changes. Following these <italic>in vitro</italic> passages, we collected the selected parasites, isolated RNAs from each population, and performed cDNA synthesis and qPCR on them. <xref rid="f0015" ref-type="fig">Fig. 3</xref>C shows the results, with wild type <italic>L. braziliensis</italic> PER002cl7 as control. We observe no difference between the unselected population bearing the transgene and the population selected under G418, indicating that the transgene is stable for >4 weeks without selection. The mRNA levels are 3-fold elevated compared with the wild type control population. Under Sb<sup>III</sup> selection, however, ARM58 mRNA levels increase significantly to 800% of wild type expression. This is good indication that the <italic>ARM58</italic> gene is indeed selected under Sb<sup>III</sup> pressure. Lacking an ARM58-specific antibody, we can only assume that those changes translate into higher protein levels.</p><p>Lastly, we analysed whether there may be sequence polymorphisms in <italic>ARM58</italic> causing different functionality in isolates PER002 and PER104. We amplified the <italic>ARM58</italic> open reading frame DNA from genomic DNA of either isolate and subcloned the products into plasmid pBluescript II KS+. Three plasmid clones each were subjected to sequence analysis. Indeed, both sequences differed in one base pair from the sequence published in the TriTryp database, resulting in a S235A amino acid exchange (data not shown). We also observed two base pair changes between isolates PER002 and PER104 (data not shown). However, both polymorphisms are silent as neither base pair change translates into an amino acid exchange. From these data, we conclude that ARM58 exerts its role as resistance marker in a solely quantitative manner.</p></sec><sec id="s0120"><label>3.11</label><title><italic>ARM58</italic> is unique to the Leishmaniae</title><p>The chromosomal region harbouring <italic>ARM58</italic> is syntenic for at least 5 <italic>Leishmania</italic> species (<xref rid="f0020" ref-type="fig">Fig. 4</xref>A), although usually found on larger chromosomes, i.e. CHR33 in the New World species <italic>L. mexicana</italic> and CHR34 in the Old World Leishmaniae <italic>L. infantum</italic>, <italic>L. major,</italic> and <italic>L. tarentolae</italic>. Upstream of <italic>ARM58,</italic> a structurally related gene, LbrM20.0200, is found that does not confer antimony resistance (<xref rid="f0005" ref-type="fig">Fig. 1</xref>D, construct (d)). We dubbed this gene <italic>ARM58rel</italic> (ARM58-related). While <italic>ARM58</italic> is notably absent from the corresponding <italic>T. brucei</italic> region, <italic>ARM58rel</italic> is present. Thus, <italic>ARM58</italic> is unique to <italic>Leishmania</italic> spp.</p><p><italic>ARM58</italic> and <italic>ARM58rel</italic> form distinct lineages (<xref rid="f0020" ref-type="fig">Fig. 4</xref>B) and show considerable sequence divergence. The gene products, ARM58 and ARM58rel, consist of four similar domains of unknown function, DUF1935. This type of domain is also found singly in various calpain-like cysteine peptidases, also described as SMPs (<xref rid="b0240" ref-type="bibr">Tull et al., 2004</xref>). However, an arrangement of four DUF1935 is exclusive to ARM58 and ARM58rel. Comparing the two putative amino acid sequences domain by domain, there is no obvious candidate domain for the drug resistance functionality. The degree of amino acid conservation in the DUF1935 varies between 56% and 64%, with the fourth DUF1935 being the least conserved (<xref rid="f0020" ref-type="fig">Fig. 4</xref>C). Also, an insertion between DUF1935-III and DUF1935-IV is unique to ARM58. Moreover, a search for possible transmembrane domains (<xref rid="b0105" ref-type="bibr">Hofmann and Stoffel, 1993</xref>) identified a candidate TMD within DUF1935-III (<xref rid="f0020" ref-type="fig">Fig. 4</xref>D).</p></sec></sec><sec sec-type="discussion" id="s0125"><label>4</label><title>Discussion</title><p>Resistance against antimony-based antileishmanial drugs was first noted in Northern India in the 1970s and has since reached alarming numbers. In high-endemicity areas the percentage of non-responders can exceed 60% rendering this mainstay treatment unusable (<xref rid="b0070" ref-type="bibr">Croft et al., 2006</xref>).</p><p>Several molecules have been reported as effectors of antimony tolerance. The multi-drug resistance (MDR) loci that encode membrane-associated P-glycoproteins were shown to play a role in laboratory induced resistance (<xref rid="b0135 b0180" ref-type="bibr">Legare et al., 2001; Ouellette et al., 2001</xref>). Gene copy number and the resulting increased expression of P-glycoproteins rendered promastigotes more resistant against Sb<sup>V</sup>. Abundance of aquaglyceroporins is inversely correlated with antimony resistance (<xref rid="b0085" ref-type="bibr">Gourbal et al., 2004</xref>). Also, expression levels of the cytosolic chaperones Hsp70 and Hsp90 were reported to correlate with antimony tolerance (<xref rid="b0045 b0265" ref-type="bibr">Brochu et al., 2004; Vergnes et al., 2007</xref>) suggesting that the protective effects of chaperones may ameliorate toxicity. A very large protein, P299, confers Sb<sup>III</sup> and Miltefosine resistance when overexpressed in <italic>L. infantum</italic> (<xref rid="b0050" ref-type="bibr">Choudhury et al., 2008</xref>). Yet another resistance mechanism seems to involve the parasite-mediated activation of host P-glycoproteins that will extrude Sb<sup>V</sup> before it can be reduced to the toxic form, Sb<sup>III</sup> (<xref rid="b0165" ref-type="bibr">Mookerjee Basu et al., 2008</xref>).</p><p>Our <italic>in vitro</italic> selection screens using two cosmid libraries of genomic DNA from resistant or sensitive <italic>L. braziliensis</italic> isolates identified a single genomic region from chromosome 20 of <italic>L. braziliensis</italic>. Episomal transgenes derived from this region confer Sb<sup>III</sup> resistance not only to <italic>L. braziliensis</italic>, but also to other species such as <italic>L.</italic> (<italic>Viannia</italic>) <italic>peruviana</italic> and a European isolate of <italic>L. infantum</italic>.</p><p>It is most interesting that in five selection screens using three host parasite strains and two libraries, only LbrM20.0210-containing cosmids dominated the surviving populations. We have no evidence that any of the established or suspected antimony resistance markers was selected in our screens. Given the rather stringent selection protocol using Sb<sup>III</sup> at 90 μM (>95% growth inhibition), our screen may not reflect the typical protocol for raising spontaneous drug resistant strains by gradually increasing the drug concentration (<xref rid="b0100 b0040" ref-type="bibr">Haimeur et al., 2000; Brochu et al., 2003</xref>). It is possible that some of the known markers were not well represented in the library, but it would be unlikely that none of them were present in the cosmid libraries since the calculated representation of genes exceeded 99% in the recombinant populations. Therefore, <italic>ARM58</italic> appears to be a dominant marker of Sb<sup>III</sup> resistance conferring unparalleled protection under stringent selection.</p><p>The product of <italic>ARM58</italic> confers increased tolerance to both Sb<sup>III</sup> and Sb<sup>V</sup>, regardless of whether the gene originated in strain PER104 or PER002. This was in keeping with the results of a sequence comparison between the <italic>ARM58</italic> homologues from PER104 and PER002 which yielded identical putative amino acid sequences and ruled out <italic>ARM58</italic> sequence polymorphisms as cause for varying resistance phenotypes.</p><p>On the other hand, we did not see any variation of ARM58 expression, at least at the RNA level. Nevertheless, selection of the <italic>ARM58</italic> transgenic parasites under Sb<sup>III</sup> resulted in an increased expression, presumably by selection for higher transgene copy numbers (<xref rid="f0015" ref-type="fig">Fig. 3</xref>C). In the field, gene copy numbers can also vary, even within isolates, based on a highly variable chromosome ploidy in <italic>Leishmania</italic> spp. (<xref rid="b0255 b0140 b0215 b0160" ref-type="bibr">Ubeda et al., 2008; Leprohon et al., 2009; Rogers et al., 2011; Mannaert et al., 2012</xref>). Therefore, our results do not rule out a natural amplification of chromosome 20 or parts thereof under antimony challenge.</p><p>ARM58 functionality is not restricted to Sb<sup>III</sup>-sensitive <italic>L. braziliensis</italic> acceptor strains either. It could also confer Sb<sup>III</sup> and Sb<sup>V</sup> resistance to <italic>L. infantum</italic>. While there is a high degree of synteny in this genomic region between <italic>Leishmania</italic> species (<xref rid="f0020" ref-type="fig">Fig. 4</xref>A), the amino acid sequence identity between the <italic>L. braziliensis</italic> and <italic>L. infantum</italic> orthologs is only 81%, with 7% similar amino acids (data not shown), underscoring the evolutionary distance between <italic>sensu stricto</italic> Leishmaniae and the <italic>Viannia</italic> subgenus.</p><p>We have tried to obtain information regarding the subcellular localisation of ARM58. We produced polyclonal antibodies against the protein after expression in <italic>E. coli</italic>. The antibodies recognise the recombinantly expressed protein with good specificity and sensitivity. However, no signals were obtained in Western blots of <italic>Leishmania</italic> cell lysates (Schäfer, unpublished data), suggesting post-translational modification of ARM58 in <italic>Leishmania</italic>. Another <italic>Leishmania</italic> protein sharing a single DUF1935, SMP-1 (Small Myristoylated Protein), forms a β-sandwich structure (<xref rid="b0080 b0245" ref-type="bibr">Gooley et al., 2006; Tull et al., 2010</xref>), bears post-translational modifications such as myristoylation (<xref rid="b0240" ref-type="bibr">Tull et al., 2004</xref>) and associates with the flagellar membrane (<xref rid="b0245 b0250" ref-type="bibr">Tull et al., 2010, 2012</xref>). It is conceivable that ARM58 with its four DUF1935 might also be membrane associated. Indeed, a ARM58::mCHERRY fusion protein localises close to the flagellar pocket in <italic>L. infantum</italic> (<xref rid="b9000" ref-type="bibr">Schäfer et al., 2013</xref>).</p><p>A dedicated deletion mutational analysis is required to find out whether one or more of the DUF1935 in ARM58 is mediating antimony resistance and whether the insertion sequence between DUF1935-III and DUF1935-IV plays any role. Given the discouraging experience with <italic>L. braziliensis</italic> as acceptor organisms for short episomal transgenes, such analyses will be carried out in a better suited model, i.e. <italic>L. infantum</italic>. Indeed, the <italic>L. infantum</italic> ortholog of <italic>ARM58, LinJ34.0220</italic>, is also capable of conferring antimony resistance and has been subject to deletion mutagenesis as well as cell biological analysis (<xref rid="b9000" ref-type="bibr">Schäfer et al., 2013</xref>).</p><p>A remaining question is whether expression rates and/or gene copy numbers for <italic>ARM58</italic> or its orthologs in other Leishmaniae varies between natural drug sensitive and drug resistant isolates. This should be investigated by using isolates from hot spots of drug resistance, such as Northern India (<xref rid="b0070" ref-type="bibr">Croft et al., 2006</xref>), and using <italic>L. donovani</italic>.</p><p>Our experience shows that the <italic>Viannia</italic> subgenus (i.e. <italic>L. braziliensis</italic> complex) is less accommodating for functional cloning than Old World <italic>Leishmania</italic> or <italic>L. mexicana</italic> complex members. While the selection of full-length cosmids appeared to work reliably – 5 independent screens identified the same genomic region – we encountered problems with decreasing length gDNA inserts. This problem persisted even when different vectors were used (not shown) and irrespective of the number of <italic>in vitro</italic> passages to which the recombinant strains were subjected. It is possible that shorter gDNA sections are more likely to give rise to antisense RNA production which would then interfere with the stability of sense transcripts (<xref rid="b0185 b0150" ref-type="bibr">Peacock et al., 2007; Lye et al., 2010</xref>). Considering our limited experience we propose to restrict functional cloning in <italic>L. braziliensis</italic> to the primary screens with full length cosmids. For subsequent steps, Old World <italic>Leishmania</italic> spp. can be used as acceptor cells. Alternatively, gene integration strategies may be employed similar to the situation with <italic>T. brucei</italic> (<xref rid="b0055" ref-type="bibr">Clayton, 1999</xref>).</p></sec><sec sec-type="conclusions" id="s0130"><label>5</label><title>Conclusion</title><p>In spite of a strategy aimed at identifying structurally distinct drug resistance markers from resistant versus sensitive <italic>L. braziliensis</italic> isolates, the screen yielded a marker gene that acts in a gene dose-dependent manner. The gene codes for a hypothetical protein of 58 kD comprising four structurally related DUF1935 domains, with one possible trans-membrane domain. The gene and its product are functionally conserved in Old World and New World <italic>Leishmania</italic> spp., but not beyond. <italic>ARM58</italic> overexpression protects both free living promastigotes and intracellular amastigotes against the effects of Sb<sup>III</sup> and Sb<sup>V</sup> respectively. More must be learned about the impact of ARM58 <italic>in vivo,</italic> its possible role in clinical antimony treatment failure, its function in antimony tolerance and the significance of its tetra-partite domain structure.</p></sec></body><back><ref-list><title>References</title><ref id="b0005"><element-citation publication-type="journal" id="h0005"><person-group person-group-type="author"><name><surname>Adaui</surname><given-names>V.</given-names></name><name><surname>Castillo</surname><given-names>D.</given-names></name><name><surname>Zimic</surname><given-names>M.</given-names></name><name><surname>Gutierrez</surname><given-names>A.</given-names></name><name><surname>Decuypere</surname><given-names>S.</given-names></name><name><surname>Vanaerschot</surname><given-names>M.</given-names></name><name><surname>De Doncker</surname><given-names>S.</given-names></name><name><surname>Schnorbusch</surname><given-names>K.</given-names></name><name><surname>Maes</surname><given-names>I.</given-names></name><name><surname>Van der Auwera</surname><given-names>G.</given-names></name><name><surname>Maes</surname><given-names>L.</given-names></name><name><surname>Llanos-Cuentas</surname><given-names>A.</given-names></name><name><surname>Arevalo</surname><given-names>J.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name></person-group><article-title>Comparative gene expression analysis throughout the life cycle of <italic>Leishmania braziliensis</italic>: diversity of expression profiles among clinical isolates</article-title><source>PLoS Negl. Trop. Dis.</source><volume>5</volume><year>2011</year><fpage>e1021</fpage><pub-id pub-id-type="pmid">21572980</pub-id></element-citation></ref><ref id="b0010"><element-citation publication-type="journal" id="h0010"><person-group person-group-type="author"><name><surname>Adaui</surname><given-names>V.</given-names></name><name><surname>Maes</surname><given-names>I.</given-names></name><name><surname>Huyse</surname><given-names>T.</given-names></name><name><surname>Van den Broeck</surname><given-names>F.</given-names></name><name><surname>Talledo</surname><given-names>M.</given-names></name><name><surname>Kuhls</surname><given-names>K.</given-names></name><name><surname>De Doncker</surname><given-names>S.</given-names></name><name><surname>Maes</surname><given-names>L.</given-names></name><name><surname>Llanos-Cuentas</surname><given-names>A.</given-names></name><name><surname>Schonian</surname><given-names>G.</given-names></name><name><surname>Arevalo</surname><given-names>J.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name></person-group><article-title>Multilocus genotyping reveals a polyphyletic pattern among naturally antimony-resistant <italic>Leishmania braziliensis</italic> isolates from Peru</article-title><source>Infect. Genet. Evol.</source><volume>11</volume><year>2011</year><fpage>1873</fpage><lpage>1880</lpage><pub-id pub-id-type="pmid">21871584</pub-id></element-citation></ref><ref id="b0015"><element-citation publication-type="journal" id="h0015"><person-group person-group-type="author"><name><surname>Adaui</surname><given-names>V.</given-names></name><name><surname>Schnorbusch</surname><given-names>K.</given-names></name><name><surname>Zimic</surname><given-names>M.</given-names></name><name><surname>Gutierrez</surname><given-names>A.</given-names></name><name><surname>Decuypere</surname><given-names>S.</given-names></name><name><surname>Vanaerschot</surname><given-names>M.</given-names></name><name><surname>DE Doncker</surname><given-names>S.</given-names></name><name><surname>Maes</surname><given-names>I.</given-names></name><name><surname>Llanos-Cuentas</surname><given-names>A.</given-names></name><name><surname>Chappuis</surname><given-names>F.</given-names></name><name><surname>Arevalo</surname><given-names>J.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name></person-group><article-title>Comparison of gene expression patterns among <italic>Leishmania braziliensis</italic> clinical isolates showing a different in vitro susceptibility to pentavalent antimony</article-title><source>Parasitology</source><volume>138</volume><year>2011</year><fpage>183</fpage><lpage>193</lpage><pub-id pub-id-type="pmid">20678296</pub-id></element-citation></ref><ref id="b0020"><element-citation publication-type="journal" id="h0020"><person-group person-group-type="author"><name><surname>Alvar</surname><given-names>J.</given-names></name><name><surname>Velez</surname><given-names>I.D.</given-names></name><name><surname>Bern</surname><given-names>C.</given-names></name><name><surname>Herrero</surname><given-names>M.</given-names></name><name><surname>Desjeux</surname><given-names>P.</given-names></name><name><surname>Cano</surname><given-names>J.</given-names></name><name><surname>Jannin</surname><given-names>J.</given-names></name><name><surname>den Boer</surname><given-names>M.</given-names></name></person-group><article-title>Leishmaniasis worldwide and global estimates of its incidence</article-title><source>PLoS ONE</source><volume>7</volume><year>2012</year><fpage>e35671</fpage><pub-id pub-id-type="pmid">22693548</pub-id></element-citation></ref><ref id="b0025"><element-citation publication-type="journal" id="h0025"><person-group person-group-type="author"><name><surname>Arevalo</surname><given-names>J.</given-names></name><name><surname>Ramirez</surname><given-names>L.</given-names></name><name><surname>Adaui</surname><given-names>V.</given-names></name><name><surname>Zimic</surname><given-names>M.</given-names></name><name><surname>Tulliano</surname><given-names>G.</given-names></name><name><surname>Miranda-Verastegui</surname><given-names>C.</given-names></name><name><surname>Lazo</surname><given-names>M.</given-names></name><name><surname>Loayza-Muro</surname><given-names>R.</given-names></name><name><surname>De Doncker</surname><given-names>S.</given-names></name><name><surname>Maurer</surname><given-names>A.</given-names></name><name><surname>Chappuis</surname><given-names>F.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name><name><surname>Llanos-Cuentas</surname><given-names>A.</given-names></name></person-group><article-title>Influence of <italic>Leishmania</italic> (Viannia) species on the response to antimonial treatment in patients with American tegumentary leishmaniasis</article-title><source>J. Infect. Dis.</source><volume>195</volume><year>2007</year><fpage>1846</fpage><lpage>1851</lpage><pub-id pub-id-type="pmid">17492601</pub-id></element-citation></ref><ref id="b0030"><element-citation publication-type="journal" id="h0030"><person-group person-group-type="author"><name><surname>Azeredo-Coutinho</surname><given-names>R.B.</given-names></name><name><surname>Mendonca</surname><given-names>S.C.</given-names></name><name><surname>Callahan</surname><given-names>H.</given-names></name><name><surname>Portal</surname><given-names>A.C.</given-names></name><name><surname>Max</surname><given-names>G.</given-names></name></person-group><article-title>Sensitivity of <italic>Leishmania braziliensis</italic> promastigotes to meglumine antimoniate (glucantime) is higher than that of other <italic>Leishmania</italic> species and correlates with response to therapy in American tegumentary leishmaniasis</article-title><source>J. Parasitol.</source><volume>93</volume><year>2007</year><fpage>688</fpage><lpage>693</lpage><pub-id pub-id-type="pmid">17626365</pub-id></element-citation></ref><ref id="b0035"><element-citation publication-type="journal" id="h0035"><person-group person-group-type="author"><name><surname>Beverley</surname><given-names>S.M.</given-names></name></person-group><article-title>Protozomics: trypanosomatid parasite genetics comes of age</article-title><source>Nat. Rev. Genet.</source><volume>4</volume><year>2003</year><fpage>11</fpage><lpage>19</lpage><pub-id pub-id-type="pmid">12509749</pub-id></element-citation></ref><ref id="b0040"><element-citation publication-type="journal" id="h0040"><person-group person-group-type="author"><name><surname>Brochu</surname><given-names>C.</given-names></name><name><surname>Wang</surname><given-names>J.</given-names></name><name><surname>Roy</surname><given-names>G.</given-names></name><name><surname>Messier</surname><given-names>N.</given-names></name><name><surname>Wang</surname><given-names>X.Y.</given-names></name><name><surname>Saravia</surname><given-names>N.G.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name></person-group><article-title>Antimony uptake systems in the protozoan parasite <italic>Leishmania</italic> and accumulation differences in antimony-resistant parasites</article-title><source>Antimicrob. Agents Chemother.</source><volume>47</volume><year>2003</year><fpage>3073</fpage><lpage>3079</lpage><pub-id pub-id-type="pmid">14506011</pub-id></element-citation></ref><ref id="b0045"><element-citation publication-type="journal" id="h0045"><person-group person-group-type="author"><name><surname>Brochu</surname><given-names>C.</given-names></name><name><surname>Haimeur</surname><given-names>A.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name></person-group><article-title>The heat shock protein HSP70 and heat shock cognate protein HSC70 contribute to antimony tolerance in the protozoan parasite leishmania</article-title><source>Cell Stress Chaperones</source><volume>9</volume><year>2004</year><fpage>294</fpage><lpage>303</lpage><pub-id pub-id-type="pmid">15544167</pub-id></element-citation></ref><ref id="b0050"><element-citation publication-type="journal" id="h0050"><person-group person-group-type="author"><name><surname>Choudhury</surname><given-names>K.</given-names></name><name><surname>Zander</surname><given-names>D.</given-names></name><name><surname>Kube</surname><given-names>M.</given-names></name><name><surname>Reinhardt</surname><given-names>R.</given-names></name><name><surname>Clos</surname><given-names>J.</given-names></name></person-group><article-title>Identification of a <italic>Leishmania infantum</italic> gene mediating resistance to miltefosine and SbIII</article-title><source>Int. J. Parasitol.</source><volume>38</volume><year>2008</year><fpage>1411</fpage><lpage>1423</lpage><pub-id pub-id-type="pmid">18457839</pub-id></element-citation></ref><ref id="b0055"><element-citation publication-type="journal" id="h0055"><person-group person-group-type="author"><name><surname>Clayton</surname><given-names>C.E.</given-names></name></person-group><article-title>Genetic manipulation of kinetoplastida</article-title><source>Parasitol. Today</source><volume>15</volume><year>1999</year><fpage>372</fpage><lpage>378</lpage><pub-id pub-id-type="pmid">10461166</pub-id></element-citation></ref><ref id="b0060"><element-citation publication-type="journal" id="h0060"><person-group person-group-type="author"><name><surname>Clayton</surname><given-names>C.E.</given-names></name></person-group><article-title>Life without transcriptional control? From fly to man and back again</article-title><source>EMBO J.</source><volume>21</volume><year>2002</year><fpage>1881</fpage><lpage>1888</lpage><pub-id pub-id-type="pmid">11953307</pub-id></element-citation></ref><ref id="b0065"><element-citation publication-type="journal" id="h0065"><person-group person-group-type="author"><name><surname>Clos</surname><given-names>J.</given-names></name><name><surname>Choudhury</surname><given-names>K.</given-names></name></person-group><article-title>Functional cloning as a means to identify <italic>Leishmania</italic> genes involved in drug resistance</article-title><source>Mini Rev. Med. Chem.</source><volume>6</volume><year>2006</year><fpage>123</fpage><lpage>129</lpage><pub-id pub-id-type="pmid">16472181</pub-id></element-citation></ref><ref id="b0070"><element-citation publication-type="journal" id="h0070"><person-group person-group-type="author"><name><surname>Croft</surname><given-names>S.L.</given-names></name><name><surname>Sundar</surname><given-names>S.</given-names></name><name><surname>Fairlamb</surname><given-names>A.H.</given-names></name></person-group><article-title>Drug resistance in leishmaniasis</article-title><source>Clin. Microbiol. Rev.</source><volume>19</volume><year>2006</year><fpage>111</fpage><lpage>126</lpage><pub-id pub-id-type="pmid">16418526</pub-id></element-citation></ref><ref id="b0075"><element-citation publication-type="journal" id="h0075"><person-group person-group-type="author"><name><surname>Garin</surname><given-names>Y.J.</given-names></name><name><surname>Sulahian</surname><given-names>A.</given-names></name><name><surname>Pratlong</surname><given-names>F.</given-names></name><name><surname>Meneceur</surname><given-names>P.</given-names></name><name><surname>Gangneux</surname><given-names>J.P.</given-names></name><name><surname>Prina</surname><given-names>E.</given-names></name><name><surname>Dedet</surname><given-names>J.P.</given-names></name><name><surname>Derouin</surname><given-names>F.</given-names></name></person-group><article-title>Virulence of <italic>Leishmania infantum</italic> is expressed as a clonal and dominant phenotype in experimental infections</article-title><source>Infect. Immun.</source><volume>69</volume><year>2001</year><fpage>7365</fpage><lpage>7373</lpage><pub-id pub-id-type="pmid">11705909</pub-id></element-citation></ref><ref id="b0080"><element-citation publication-type="journal" id="h0080"><person-group person-group-type="author"><name><surname>Gooley</surname><given-names>P.R.</given-names></name><name><surname>Mertens</surname><given-names>H.D.</given-names></name><name><surname>Tull</surname><given-names>D.</given-names></name><name><surname>McConville</surname><given-names>M.J.</given-names></name></person-group><article-title><sup>1</sup>H, <sup>13</sup>C and <sup>15</sup>N resonance assignments of SMP-1: a small myristoylated protein from Leishmania major</article-title><source>J. Biomol. NMR</source><volume>36</volume><issue>Suppl. 1</issue><year>2006</year><fpage>26</fpage><pub-id pub-id-type="pmid">16601858</pub-id></element-citation></ref><ref id="b0085"><element-citation publication-type="journal" id="h0085"><person-group person-group-type="author"><name><surname>Gourbal</surname><given-names>B.</given-names></name><name><surname>Sonuc</surname><given-names>N.</given-names></name><name><surname>Bhattacharjee</surname><given-names>H.</given-names></name><name><surname>Legare</surname><given-names>D.</given-names></name><name><surname>Sundar</surname><given-names>S.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name><name><surname>Rosen</surname><given-names>B.P.</given-names></name><name><surname>Mukhopadhyay</surname><given-names>R.</given-names></name></person-group><article-title>Drug uptake and modulation of drug resistance in <italic>Leishmania</italic> by an aquaglyceroporin</article-title><source>J. Biol. Chem.</source><volume>279</volume><year>2004</year><fpage>31010</fpage><lpage>31017</lpage><pub-id pub-id-type="pmid">15138256</pub-id></element-citation></ref><ref id="b0090"><element-citation publication-type="journal" id="h0090"><person-group person-group-type="author"><name><surname>Grondin</surname><given-names>K.</given-names></name><name><surname>Haimeur</surname><given-names>A.</given-names></name><name><surname>Mukhopadhyay</surname><given-names>R.</given-names></name><name><surname>Rosen</surname><given-names>B.P.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name></person-group><article-title>Co-amplification of the gamma-glutamylcysteine synthetase gene gsh1 and of the ABC transporter gene pgpA in arsenite-resistant <italic>Leishmania tarentolae</italic></article-title><source>EMBO J.</source><volume>16</volume><year>1997</year><fpage>3057</fpage><lpage>3065</lpage><pub-id pub-id-type="pmid">9214623</pub-id></element-citation></ref><ref id="b0095"><element-citation publication-type="journal" id="h0095"><person-group person-group-type="author"><name><surname>Haimeur</surname><given-names>A.</given-names></name><name><surname>Guimond</surname><given-names>C.</given-names></name><name><surname>Pilote</surname><given-names>S.</given-names></name><name><surname>Mukhopadhyay</surname><given-names>R.</given-names></name><name><surname>Rosen</surname><given-names>B.P.</given-names></name><name><surname>Poulin</surname><given-names>R.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name></person-group><article-title>Elevated levels of polyamines and trypanothione resulting from overexpression of the ornithine decarboxylase gene in arsenite-resistant <italic>Leishmania</italic></article-title><source>Mol. Microbiol.</source><volume>34</volume><year>1999</year><fpage>726</fpage><lpage>735</lpage><pub-id pub-id-type="pmid">10564512</pub-id></element-citation></ref><ref id="b0100"><element-citation publication-type="journal" id="h0100"><person-group person-group-type="author"><name><surname>Haimeur</surname><given-names>A.</given-names></name><name><surname>Brochu</surname><given-names>C.</given-names></name><name><surname>Genest</surname><given-names>P.</given-names></name><name><surname>Papadopoulou</surname><given-names>B.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name></person-group><article-title>Amplification of the ABC transporter gene PGPA and increased trypanothione levels in potassium antimonyl tartrate (SbIII) resistant <italic>Leishmania tarentolae</italic></article-title><source>Mol. Biochem. Parasitol.</source><volume>108</volume><year>2000</year><fpage>131</fpage><lpage>135</lpage><pub-id pub-id-type="pmid">10802326</pub-id></element-citation></ref><ref id="b0105"><element-citation publication-type="journal" id="h0105"><person-group person-group-type="author"><name><surname>Hofmann</surname><given-names>K.</given-names></name><name><surname>Stoffel</surname><given-names>W.</given-names></name></person-group><article-title>TMBASE – a database of membrane spanning protein segments</article-title><source>Biol. Chem. Hoppe-Seyler</source><volume>374</volume><year>1993</year><fpage>166</fpage></element-citation></ref><ref id="b0110"><element-citation publication-type="journal" id="h0110"><person-group person-group-type="author"><name><surname>Hoyer</surname><given-names>C.</given-names></name><name><surname>Mellenthin</surname><given-names>K.</given-names></name><name><surname>Schilhabel</surname><given-names>M.</given-names></name><name><surname>Platzer</surname><given-names>M.</given-names></name><name><surname>Clos</surname><given-names>J.</given-names></name></person-group><article-title><italic>Leishmania</italic> and the Leishmaniases: Use of genetic complementation to identify gene(s) which specify species-specific organ tropism of <italic>Leishmania</italic></article-title><source>Med. Microbiol. Immunol.</source><volume>190</volume><year>2001</year><fpage>53</fpage><lpage>56</lpage></element-citation></ref><ref id="b0115"><element-citation publication-type="journal" id="h0115"><person-group person-group-type="author"><name><surname>Kapler</surname><given-names>G.M.</given-names></name><name><surname>Coburn</surname><given-names>C.M.</given-names></name><name><surname>Beverley</surname><given-names>S.M.</given-names></name></person-group><article-title>Stable transfection of the human parasite <italic>Leishmania major</italic> delineates a 30-kilobase region sufficient for extrachromosomal replication and expression</article-title><source>Mol. Cell. Biol.</source><volume>10</volume><year>1990</year><fpage>1084</fpage><lpage>1094</lpage><pub-id pub-id-type="pmid">2304458</pub-id></element-citation></ref><ref id="b0120"><element-citation publication-type="journal" id="h0120"><person-group person-group-type="author"><name><surname>Kelly</surname><given-names>J.M.</given-names></name><name><surname>Das</surname><given-names>P.</given-names></name><name><surname>Tomás</surname><given-names>A.M.</given-names></name></person-group><article-title>An approach to functional complementation by introduction of large DNA fragments into <italic>Trypanosoma cruzi</italic> and <italic>Leishmania donovani</italic> using a cosmid shuttle vector</article-title><source>Mol. Biochem. Parasitol.</source><volume>65</volume><year>1994</year><fpage>51</fpage><lpage>62</lpage><pub-id pub-id-type="pmid">7935628</pub-id></element-citation></ref><ref id="b0125"><element-citation publication-type="journal" id="h0125"><person-group person-group-type="author"><name><surname>Krobitsch</surname><given-names>S.</given-names></name><name><surname>Brandau</surname><given-names>S.</given-names></name><name><surname>Hoyer</surname><given-names>C.</given-names></name><name><surname>Schmetz</surname><given-names>C.</given-names></name><name><surname>Hübel</surname><given-names>A.</given-names></name><name><surname>Clos</surname><given-names>J.</given-names></name></person-group><article-title><italic>Leishmania donovani</italic> heat shock protein 100: characterization and function in amastigote stage differentiation</article-title><source>J. Biol. Chem.</source><volume>273</volume><year>1998</year><fpage>6488</fpage><lpage>6494</lpage><pub-id pub-id-type="pmid">9497383</pub-id></element-citation></ref><ref id="b0130"><element-citation publication-type="journal" id="h0130"><person-group person-group-type="author"><name><surname>Laban</surname><given-names>A.</given-names></name><name><surname>Wirth</surname><given-names>D.F.</given-names></name></person-group><article-title>Transfection of <italic>Leishmania enriettii</italic> and expression of chloramphenicol acetyltransferase gene</article-title><source>Proc. Natl. Acad. Sci. USA</source><volume>86</volume><year>1989</year><fpage>9119</fpage><lpage>9123</lpage><pub-id pub-id-type="pmid">2594753</pub-id></element-citation></ref><ref id="b0135"><element-citation publication-type="journal" id="h0135"><person-group person-group-type="author"><name><surname>Legare</surname><given-names>D.</given-names></name><name><surname>Cayer</surname><given-names>S.</given-names></name><name><surname>Singh</surname><given-names>A.K.</given-names></name><name><surname>Richard</surname><given-names>D.</given-names></name><name><surname>Papadopoulou</surname><given-names>B.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name></person-group><article-title>ABC proteins of Leishmania</article-title><source>J. Bioenergy Biomembr.</source><volume>33</volume><year>2001</year><fpage>469</fpage><lpage>474</lpage></element-citation></ref><ref id="b0140"><element-citation publication-type="journal" id="h0140"><person-group person-group-type="author"><name><surname>Leprohon</surname><given-names>P.</given-names></name><name><surname>Legare</surname><given-names>D.</given-names></name><name><surname>Raymond</surname><given-names>F.</given-names></name><name><surname>Madore</surname><given-names>E.</given-names></name><name><surname>Hardiman</surname><given-names>G.</given-names></name><name><surname>Corbeil</surname><given-names>J.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name></person-group><article-title>Gene expression modulation is associated with gene amplification, supernumerary chromosomes and chromosome loss in antimony-resistant <italic>Leishmania infantum</italic></article-title><source>Nucl. Acids Res.</source><volume>37</volume><year>2009</year><fpage>1387</fpage><lpage>1399</lpage><pub-id pub-id-type="pmid">19129236</pub-id></element-citation></ref><ref id="b0145"><element-citation publication-type="journal" id="h0145"><person-group person-group-type="author"><name><surname>Llanos-Cuentas</surname><given-names>A.</given-names></name><name><surname>Tulliano</surname><given-names>G.</given-names></name><name><surname>Araujo-Castillo</surname><given-names>R.</given-names></name><name><surname>Miranda-Verastegui</surname><given-names>C.</given-names></name><name><surname>Santamaria-Castrellon</surname><given-names>G.</given-names></name><name><surname>Ramirez</surname><given-names>L.</given-names></name><name><surname>Lazo</surname><given-names>M.</given-names></name><name><surname>De Doncker</surname><given-names>S.</given-names></name><name><surname>Boelaert</surname><given-names>M.</given-names></name><name><surname>Robays</surname><given-names>J.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name><name><surname>Arevalo</surname><given-names>J.</given-names></name><name><surname>Chappuis</surname><given-names>F.</given-names></name></person-group><article-title>Clinical and parasite species risk factors for pentavalent antimonial treatment failure in cutaneous leishmaniasis in Peru</article-title><source>Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America</source><volume>46</volume><year>2008</year><fpage>223</fpage><lpage>231</lpage><pub-id pub-id-type="pmid">18171254</pub-id></element-citation></ref><ref id="b0150"><element-citation publication-type="journal" id="h0150"><person-group person-group-type="author"><name><surname>Lye</surname><given-names>L.F.</given-names></name><name><surname>Owens</surname><given-names>K.</given-names></name><name><surname>Shi</surname><given-names>H.</given-names></name><name><surname>Murta</surname><given-names>S.M.</given-names></name><name><surname>Vieira</surname><given-names>A.C.</given-names></name><name><surname>Turco</surname><given-names>S.J.</given-names></name><name><surname>Tschudi</surname><given-names>C.</given-names></name><name><surname>Ullu</surname><given-names>E.</given-names></name><name><surname>Beverley</surname><given-names>S.M.</given-names></name></person-group><article-title>Retention and loss of RNA interference pathways in trypanosomatid protozoans</article-title><source>PLoS Pathogens</source><volume>6</volume><year>2010</year><fpage>e1001161</fpage><pub-id pub-id-type="pmid">21060810</pub-id></element-citation></ref><ref id="b0155"><element-citation publication-type="journal" id="h0155"><person-group person-group-type="author"><name><surname>Mann</surname><given-names>H.B.</given-names></name><name><surname>Whitney</surname><given-names>D.R.</given-names></name></person-group><article-title>On a test of whether one of two random variables is stochastically larger than the other</article-title><source>Ann. Math. Stat.</source><volume>18</volume><year>1947</year><fpage>50</fpage><lpage>60</lpage></element-citation></ref><ref id="b0160"><element-citation publication-type="journal" id="h0160"><person-group person-group-type="author"><name><surname>Mannaert</surname><given-names>A.</given-names></name><name><surname>Downing</surname><given-names>T.</given-names></name><name><surname>Imamura</surname><given-names>H.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name></person-group><article-title>Adaptive mechanisms in pathogens: universal aneuploidy in <italic>Leishmania</italic></article-title><source>Trends Parasitol.</source><volume>28</volume><year>2012</year><fpage>370</fpage><lpage>376</lpage><pub-id pub-id-type="pmid">22789456</pub-id></element-citation></ref><ref id="b0165"><element-citation publication-type="journal" id="h0165"><person-group person-group-type="author"><name><surname>Mookerjee Basu</surname><given-names>J.</given-names></name><name><surname>Mookerjee</surname><given-names>A.</given-names></name><name><surname>Banerjee</surname><given-names>R.</given-names></name><name><surname>Saha</surname><given-names>M.</given-names></name><name><surname>Singh</surname><given-names>S.</given-names></name><name><surname>Naskar</surname><given-names>K.</given-names></name><name><surname>Tripathy</surname><given-names>G.</given-names></name><name><surname>Sinha</surname><given-names>P.K.</given-names></name><name><surname>Pandey</surname><given-names>K.</given-names></name><name><surname>Sundar</surname><given-names>S.</given-names></name><name><surname>Bimal</surname><given-names>S.</given-names></name><name><surname>Das</surname><given-names>P.K.</given-names></name><name><surname>Choudhuri</surname><given-names>S.K.</given-names></name><name><surname>Roy</surname><given-names>S.</given-names></name></person-group><article-title>Inhibition of ABC transporters abolishes antimony resistance in Leishmania infection</article-title><source>Antimicrob. Agents Chemother.</source><volume>52</volume><year>2008</year><fpage>1080</fpage><lpage>1093</lpage><pub-id pub-id-type="pmid">18056276</pub-id></element-citation></ref><ref id="b0170"><element-citation publication-type="journal" id="h0170"><person-group person-group-type="author"><name><surname>Mukherjee</surname><given-names>B.</given-names></name><name><surname>Mukhopadhyay</surname><given-names>R.</given-names></name><name><surname>Bannerjee</surname><given-names>B.</given-names></name><name><surname>Chowdhury</surname><given-names>S.</given-names></name><name><surname>Mukherjee</surname><given-names>S.</given-names></name><name><surname>Naskar</surname><given-names>K.</given-names></name><name><surname>Allam</surname><given-names>U.S.</given-names></name><name><surname>Chakravortty</surname><given-names>D.</given-names></name><name><surname>Sundar</surname><given-names>S.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name><name><surname>Roy</surname><given-names>S.</given-names></name></person-group><article-title>Antimony-resistant but not antimony-sensitive <italic>Leishmania donovani</italic> up-regulates host IL-10 to overexpress multidrug-resistant protein 1</article-title><source>Proc. Natl. Acad. Sci. USA</source><volume>110</volume><year>2013</year><fpage>E575</fpage><lpage>E582</lpage><pub-id pub-id-type="pmid">23341611</pub-id></element-citation></ref><ref id="b0175"><element-citation publication-type="journal" id="h0175"><person-group person-group-type="author"><name><surname>Ouellette</surname><given-names>M.</given-names></name><name><surname>Haimeur</surname><given-names>A.</given-names></name><name><surname>Grondin</surname><given-names>K.</given-names></name><name><surname>Legare</surname><given-names>D.</given-names></name><name><surname>Papadopoulou</surname><given-names>B.</given-names></name></person-group><article-title>Amplification of ABC transporter gene pgpA and of other heavy metal resistance genes in <italic>Leishmania tarentolae</italic> and their study by gene transfection and gene disruption</article-title><source>Methods Enzymol.</source><volume>292</volume><year>1998</year><fpage>182</fpage><lpage>193</lpage><pub-id pub-id-type="pmid">9711554</pub-id></element-citation></ref><ref id="b0180"><element-citation publication-type="journal" id="h0180"><person-group person-group-type="author"><name><surname>Ouellette</surname><given-names>M.</given-names></name><name><surname>Legare</surname><given-names>D.</given-names></name><name><surname>Papadopoulou</surname><given-names>B.</given-names></name></person-group><article-title>Multidrug resistance and ABC transporters in parasitic protozoa</article-title><source>J. Mol. Microbiol. Biotechnol.</source><volume>3</volume><year>2001</year><fpage>201</fpage><lpage>206</lpage><pub-id pub-id-type="pmid">11321574</pub-id></element-citation></ref><ref id="b0185"><element-citation publication-type="journal" id="h0185"><person-group person-group-type="author"><name><surname>Peacock</surname><given-names>C.S.</given-names></name><name><surname>Seeger</surname><given-names>K.</given-names></name><name><surname>Harris</surname><given-names>D.</given-names></name><name><surname>Murphy</surname><given-names>L.</given-names></name><name><surname>Ruiz</surname><given-names>J.C.</given-names></name><name><surname>Quail</surname><given-names>M.A.</given-names></name><name><surname>Peters</surname><given-names>N.</given-names></name><name><surname>Adlem</surname><given-names>E.</given-names></name><name><surname>Tivey</surname><given-names>A.</given-names></name><name><surname>Aslett</surname><given-names>M.</given-names></name><name><surname>Kerhornou</surname><given-names>A.</given-names></name><name><surname>Ivens</surname><given-names>A.</given-names></name><name><surname>Fraser</surname><given-names>A.</given-names></name><name><surname>Rajandream</surname><given-names>M.A.</given-names></name><name><surname>Carver</surname><given-names>T.</given-names></name><name><surname>Norbertczak</surname><given-names>H.</given-names></name><name><surname>Chillingworth</surname><given-names>T.</given-names></name><name><surname>Hance</surname><given-names>Z.</given-names></name><name><surname>Jagels</surname><given-names>K.</given-names></name><name><surname>Moule</surname><given-names>S.</given-names></name><name><surname>Ormond</surname><given-names>D.</given-names></name><name><surname>Rutter</surname><given-names>S.</given-names></name><name><surname>Squares</surname><given-names>R.</given-names></name><name><surname>Whitehead</surname><given-names>S.</given-names></name><name><surname>Rabbinowitsch</surname><given-names>E.</given-names></name><name><surname>Arrowsmith</surname><given-names>C.</given-names></name><name><surname>White</surname><given-names>B.</given-names></name><name><surname>Thurston</surname><given-names>S.</given-names></name><name><surname>Bringaud</surname><given-names>F.</given-names></name><name><surname>Baldauf</surname><given-names>S.L.</given-names></name><name><surname>Faulconbridge</surname><given-names>A.</given-names></name><name><surname>Jeffares</surname><given-names>D.</given-names></name><name><surname>Depledge</surname><given-names>D.P.</given-names></name><name><surname>Oyola</surname><given-names>S.O.</given-names></name><name><surname>Hilley</surname><given-names>J.D.</given-names></name><name><surname>Brito</surname><given-names>L.O.</given-names></name><name><surname>Tosi</surname><given-names>L.R.</given-names></name><name><surname>Barrell</surname><given-names>B.</given-names></name><name><surname>Cruz</surname><given-names>A.K.</given-names></name><name><surname>Mottram</surname><given-names>J.C.</given-names></name><name><surname>Smith</surname><given-names>D.F.</given-names></name><name><surname>Berriman</surname><given-names>M.</given-names></name></person-group><article-title>Comparative genomic analysis of three <italic>Leishmania</italic> species that cause diverse human disease</article-title><source>Nat. Genet.</source><volume>39</volume><year>2007</year><fpage>839</fpage><lpage>847</lpage><pub-id pub-id-type="pmid">17572675</pub-id></element-citation></ref><ref id="b0195"><element-citation publication-type="journal" id="h0195"><person-group person-group-type="author"><name><surname>Racoosin</surname><given-names>E.L.</given-names></name><name><surname>Swanson</surname><given-names>J.A.</given-names></name></person-group><article-title>Macrophage colony-stimulating factor (rM-CSF) stimulates pinocytosis in bone marrow-derived macrophages</article-title><source>J. Exp. Med.</source><volume>170</volume><year>1989</year><fpage>1635</fpage><lpage>1648</lpage><pub-id pub-id-type="pmid">2681516</pub-id></element-citation></ref><ref id="b0190"><element-citation publication-type="journal" id="h0190"><person-group person-group-type="author"><name><surname>Racoosin</surname><given-names>E.L.</given-names></name><name><surname>Beverley</surname><given-names>S.M.</given-names></name></person-group><article-title>Leishmania major: promastigotes induce expression of a subset of chemokine genes in murine macrophages</article-title><source>Exp. Parasitol.</source><volume>85</volume><year>1997</year><fpage>283</fpage><lpage>295</lpage><pub-id pub-id-type="pmid">9085925</pub-id></element-citation></ref><ref id="b0200"><element-citation publication-type="journal" id="h0200"><person-group person-group-type="author"><name><surname>Reiling</surname><given-names>L.</given-names></name><name><surname>Chrobak</surname><given-names>M.</given-names></name><name><surname>Schmetz</surname><given-names>C.</given-names></name><name><surname>Clos</surname><given-names>J.</given-names></name></person-group><article-title>Overexpression of a single <italic>Leishmania major</italic> gene is sufficient to enhance parasite infectivity in vivo and in vitro</article-title><source>Mol. Microbiol.</source><volume>76</volume><year>2010</year><fpage>1175</fpage><lpage>1190</lpage><pub-id pub-id-type="pmid">20345655</pub-id></element-citation></ref><ref id="b0205"><element-citation publication-type="journal" id="h0205"><person-group person-group-type="author"><name><surname>Rijal</surname><given-names>S.</given-names></name><name><surname>Yardley</surname><given-names>V.</given-names></name><name><surname>Chappuis</surname><given-names>F.</given-names></name><name><surname>Decuypere</surname><given-names>S.</given-names></name><name><surname>Khanal</surname><given-names>B.</given-names></name><name><surname>Singh</surname><given-names>R.</given-names></name><name><surname>Boelaert</surname><given-names>M.</given-names></name><name><surname>De Doncker</surname><given-names>S.</given-names></name><name><surname>Croft</surname><given-names>S.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name></person-group><article-title>Antimonial treatment of visceral leishmaniasis: are current in vitro susceptibility assays adequate for prognosis of in vivo therapy outcome?</article-title><source>Microbes Infect.</source><volume>9</volume><year>2007</year><fpage>529</fpage><lpage>535</lpage><pub-id pub-id-type="pmid">17350306</pub-id></element-citation></ref><ref id="b0210"><element-citation publication-type="journal" id="h0210"><person-group person-group-type="author"><name><surname>Roberts</surname><given-names>W.L.</given-names></name><name><surname>Berman</surname><given-names>J.D.</given-names></name><name><surname>Rainey</surname><given-names>P.M.</given-names></name></person-group><article-title>In vitro antileishmanial properties of tri- and pentavalent antimonial preparations</article-title><source>Antimicrob. Agents Chemother.</source><volume>39</volume><year>1995</year><fpage>1234</fpage><lpage>1239</lpage><pub-id pub-id-type="pmid">7574507</pub-id></element-citation></ref><ref id="b0215"><element-citation publication-type="journal" id="h0215"><person-group person-group-type="author"><name><surname>Rogers</surname><given-names>M.B.</given-names></name><name><surname>Hilley</surname><given-names>J.D.</given-names></name><name><surname>Dickens</surname><given-names>N.J.</given-names></name><name><surname>Wilkes</surname><given-names>J.</given-names></name><name><surname>Bates</surname><given-names>P.A.</given-names></name><name><surname>Depledge</surname><given-names>D.P.</given-names></name><name><surname>Harris</surname><given-names>D.</given-names></name><name><surname>Her</surname><given-names>Y.</given-names></name><name><surname>Herzyk</surname><given-names>P.</given-names></name><name><surname>Imamura</surname><given-names>H.</given-names></name><name><surname>Otto</surname><given-names>T.D.</given-names></name><name><surname>Sanders</surname><given-names>M.</given-names></name><name><surname>Seeger</surname><given-names>K.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name><name><surname>Berriman</surname><given-names>M.</given-names></name><name><surname>Smith</surname><given-names>D.F.</given-names></name><name><surname>Hertz-Fowler</surname><given-names>C.</given-names></name><name><surname>Mottram</surname><given-names>J.C.</given-names></name></person-group><article-title>Chromosome and gene copy number variation allow major structural change between species and strains of <italic>Leishmania</italic></article-title><source>Genome Res.</source><volume>21</volume><year>2011</year><fpage>2129</fpage><lpage>2142</lpage><pub-id pub-id-type="pmid">22038252</pub-id></element-citation></ref><ref id="b0220"><element-citation publication-type="book" id="h0220"><person-group person-group-type="author"><name><surname>Sambrook</surname><given-names>J.</given-names></name><name><surname>Russell</surname><given-names>D.W.</given-names></name></person-group><chapter-title>Molecular Cloning</chapter-title><edition>third ed.</edition><year>2001</year><publisher-name>Cold Spring Harbor Laboratory Press</publisher-name><publisher-loc>Cold Spring Harbor, NY</publisher-loc></element-citation></ref><ref id="b9000"><element-citation publication-type="journal" id="h9000"><person-group person-group-type="author"><name><surname>Schäfer</surname><given-names>C.</given-names></name><name><surname>Tejera Nevado</surname><given-names>P.</given-names></name><name><surname>Zander</surname><given-names>D.</given-names></name><name><surname>Clos</surname><given-names>J.</given-names></name></person-group><article-title>ARM58 Overexpression Reduces Intracellular Antimony Concentration in Leishmania infantum</article-title><source>Antimicrob Agents Chemother</source><year>2013</year><comment>submitted for publication</comment></element-citation></ref><ref id="b0225"><element-citation publication-type="journal" id="h0225"><person-group person-group-type="author"><name><surname>Shaked-Mishan</surname><given-names>P.</given-names></name><name><surname>Ulrich</surname><given-names>N.</given-names></name><name><surname>Ephros</surname><given-names>M.</given-names></name><name><surname>Zilberstein</surname><given-names>D.</given-names></name></person-group><article-title>Novel Intracellular SbV reducing activity correlates with antimony susceptibility in <italic>Leishmania donovani</italic></article-title><source>J. Biol. Chem.</source><volume>276</volume><year>2001</year><fpage>3971</fpage><lpage>3976</lpage><pub-id pub-id-type="pmid">11110784</pub-id></element-citation></ref><ref id="b0230"><element-citation publication-type="journal" id="h0230"><person-group person-group-type="author"><name><surname>Soto</surname><given-names>J.</given-names></name><name><surname>Toledo</surname><given-names>J.</given-names></name><name><surname>Vega</surname><given-names>J.</given-names></name><name><surname>Berman</surname><given-names>J.</given-names></name></person-group><article-title>Short report: efficacy of pentavalent antimony for treatment of Colombian cutaneous leishmaniasis</article-title><source>Am. J. Trop. Med. Hyg.</source><volume>72</volume><year>2005</year><fpage>421</fpage><lpage>422</lpage><pub-id pub-id-type="pmid">15827279</pub-id></element-citation></ref><ref id="b0235"><element-citation publication-type="journal" id="h0235"><person-group person-group-type="author"><name><surname>Sundar</surname><given-names>S.</given-names></name></person-group><article-title>Treatment of visceral leishmaniasis</article-title><source>Med. Microbiol. Immunol. (Berl)</source><volume>190</volume><year>2001</year><fpage>89</fpage><lpage>92</lpage><pub-id pub-id-type="pmid">11770119</pub-id></element-citation></ref><ref id="b0240"><element-citation publication-type="journal" id="h0240"><person-group person-group-type="author"><name><surname>Tull</surname><given-names>D.</given-names></name><name><surname>Vince</surname><given-names>J.E.</given-names></name><name><surname>Callaghan</surname><given-names>J.M.</given-names></name><name><surname>Naderer</surname><given-names>T.</given-names></name><name><surname>Spurck</surname><given-names>T.</given-names></name><name><surname>McFadden</surname><given-names>G.I.</given-names></name><name><surname>Currie</surname><given-names>G.</given-names></name><name><surname>Ferguson</surname><given-names>K.</given-names></name><name><surname>Bacic</surname><given-names>A.</given-names></name><name><surname>McConville</surname><given-names>M.J.</given-names></name></person-group><article-title>SMP-1, a member of a new family of small myristoylated proteins in kinetoplastid parasites, is targeted to the flagellum membrane in <italic>Leishmania</italic></article-title><source>Mol. Biol. Cell</source><volume>15</volume><year>2004</year><fpage>4775</fpage><lpage>4786</lpage><pub-id pub-id-type="pmid">15342784</pub-id></element-citation></ref><ref id="b0245"><element-citation publication-type="journal" id="h0245"><person-group person-group-type="author"><name><surname>Tull</surname><given-names>D.</given-names></name><name><surname>Naderer</surname><given-names>T.</given-names></name><name><surname>Spurck</surname><given-names>T.</given-names></name><name><surname>Mertens</surname><given-names>H.D.</given-names></name><name><surname>Heng</surname><given-names>J.</given-names></name><name><surname>McFadden</surname><given-names>G.I.</given-names></name><name><surname>Gooley</surname><given-names>P.R.</given-names></name><name><surname>McConville</surname><given-names>M.J.</given-names></name></person-group><article-title>Membrane protein SMP-1 is required for normal flagellum function in <italic>Leishmania</italic></article-title><source>J. Cell Sci.</source><volume>123</volume><year>2010</year><fpage>544</fpage><lpage>554</lpage><pub-id pub-id-type="pmid">20086045</pub-id></element-citation></ref><ref id="b0250"><element-citation publication-type="journal" id="h0250"><person-group person-group-type="author"><name><surname>Tull</surname><given-names>D.</given-names></name><name><surname>Heng</surname><given-names>J.</given-names></name><name><surname>Gooley</surname><given-names>P.R.</given-names></name><name><surname>Naderer</surname><given-names>T.</given-names></name><name><surname>McConville</surname><given-names>M.J.</given-names></name></person-group><article-title>Acylation-dependent and-independent membrane targeting and distinct functions of small myristoylated proteins (SMPs) in <italic>Leishmania major</italic></article-title><source>Int. J. Parasitol.</source><volume>42</volume><year>2012</year><fpage>239</fpage><lpage>247</lpage><pub-id pub-id-type="pmid">22281304</pub-id></element-citation></ref><ref id="b0255"><element-citation publication-type="journal" id="h0255"><person-group person-group-type="author"><name><surname>Ubeda</surname><given-names>J.M.</given-names></name><name><surname>Legare</surname><given-names>D.</given-names></name><name><surname>Raymond</surname><given-names>F.</given-names></name><name><surname>Ouameur</surname><given-names>A.A.</given-names></name><name><surname>Boisvert</surname><given-names>S.</given-names></name><name><surname>Rigault</surname><given-names>P.</given-names></name><name><surname>Corbeil</surname><given-names>J.</given-names></name><name><surname>Tremblay</surname><given-names>M.J.</given-names></name><name><surname>Olivier</surname><given-names>M.</given-names></name><name><surname>Papadopoulou</surname><given-names>B.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name></person-group><article-title>Modulation of gene expression in drug resistant <italic>Leishmania</italic> is associated with gene amplification, gene deletion and chromosome aneuploidy</article-title><source>Genome Biol.</source><volume>9</volume><year>2008</year><fpage>R115</fpage><pub-id pub-id-type="pmid">18638379</pub-id></element-citation></ref><ref id="b0260"><element-citation publication-type="journal" id="h0260"><person-group person-group-type="author"><name><surname>Ullu</surname><given-names>E.</given-names></name><name><surname>Tschudi</surname><given-names>C.</given-names></name><name><surname>Chakraborty</surname><given-names>T.</given-names></name></person-group><article-title>RNA interference in protozoan parasites</article-title><source>Cell. Microbiol.</source><volume>6</volume><year>2004</year><fpage>509</fpage><lpage>519</lpage><pub-id pub-id-type="pmid">15104593</pub-id></element-citation></ref><ref id="b0265"><element-citation publication-type="journal" id="h0265"><person-group person-group-type="author"><name><surname>Vergnes</surname><given-names>B.</given-names></name><name><surname>Gourbal</surname><given-names>B.</given-names></name><name><surname>Girard</surname><given-names>I.</given-names></name><name><surname>Sundar</surname><given-names>S.</given-names></name><name><surname>Drummelsmith</surname><given-names>J.</given-names></name><name><surname>Ouellette</surname><given-names>M.</given-names></name></person-group><article-title>A proteomics screen implicates HSP83 and a small kinetoplastid calpain-related protein in drug resistance in <italic>Leishmania donovani</italic> clinical field isolates by modulating drug-induced programmed cell death</article-title><source>Mol. Cell. Proteomics</source><volume>6</volume><year>2007</year><fpage>88</fpage><lpage>101</lpage><pub-id pub-id-type="pmid">17050524</pub-id></element-citation></ref><ref id="b0270"><element-citation publication-type="journal" id="h0270"><person-group person-group-type="author"><name><surname>Yardley</surname><given-names>V.</given-names></name><name><surname>Ortuno</surname><given-names>N.</given-names></name><name><surname>Llanos-Cuentas</surname><given-names>A.</given-names></name><name><surname>Chappuis</surname><given-names>F.</given-names></name><name><surname>Doncker</surname><given-names>S.D.</given-names></name><name><surname>Ramirez</surname><given-names>L.</given-names></name><name><surname>Croft</surname><given-names>S.</given-names></name><name><surname>Arevalo</surname><given-names>J.</given-names></name><name><surname>Adaui</surname><given-names>V.</given-names></name><name><surname>Bermudez</surname><given-names>H.</given-names></name><name><surname>Decuypere</surname><given-names>S.</given-names></name><name><surname>Dujardin</surname><given-names>J.C.</given-names></name></person-group><article-title>American tegumentary leishmaniasis: is antimonial treatment outcome related to parasite drug susceptibility?</article-title><source>J. Infect. Dis.</source><volume>194</volume><year>2006</year><fpage>1168</fpage><lpage>1175</lpage><pub-id pub-id-type="pmid">16991093</pub-id></element-citation></ref></ref-list><sec id="s0140" sec-type="supplementary-material"><label>Appendix A</label><title>Supplementary data</title><p><supplementary-material content-type="local-data" id="m0005"><caption><title>Supplementary data 1</title></caption><media xlink:href="mmc1.pdf"></media></supplementary-material></p></sec><ack id="ak005"><title>Acknowledgements</title><p>We acknowledge helpful suggestions from the members of the LeishEpiNetSA consortium. This work was funded by <funding-source id="gp005">EU</funding-source> Grant INCO-CT2005-015407-LeishEpiNet. AN was a fellow of the Deutscher Akademischer Austauschdienst (DAAD) for parts of the project. We also acknowledge expert technical assistance from Manfred Krömer (<sup>†</sup>2009) and Anne Macdonald. We thank Laura Jade Lee for a careful reading of the manuscript. We are not aware of conflicts of interest for any of the authors.</p></ack><fn-group><fn id="d32e504"><label>☆</label><p>This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.</p></fn></fn-group></back><floats-group><fig id="f0005"><label>Fig. 1</label><caption><p>(A) Sequence alignment between the experimentally determined insert sequence of pcosC1.6 and <italic>L. braziliensis</italic> chromosome 20. The 5′ ∼15 kb of the insert align in reverse complimentary direction with the 5′ end of chromosome 20, whilst the C′-terminal 24 kb align in colinear fashion with chromosome 20 sequences between positions 56 and 80 kb. (B) Schematic representation of the overlapping genomic DNA inserts of cosmid C1.6, A3 and B1. Eight open reading frames (ORFs) are present in all three cosmid inserts. The four digit gene numbers correspond to the systematic numbers for chromosome 20 (LbrM20.____) derived from version 2 of the <italic>L. braziliensis</italic> genome project. The total length of each insert (to the right in [bp]) was derived from end-sequencing. Green boxes symbolise ORFs for hypothetical proteins, orange boxes stand for conserved hypothetical proteins, and yellow boxes signify coding regions for proteins with predicted functions. Hatched boxes stand for incomplete ORFs. Vertical dotted lines connect identical ORFs found in all 3 cosmids. Note that the sequence was incomplete in the genome project, causing the apparent non-linear numbering of gene candidates. (C) Truncation of cosmid insert C1.6. The inserts of seven deletion constructs derived from the cosmid pcosC1.6 are schematically shown. The deletions are represented by the dashed lines. The positions of <italic>Afl</italic>II, <italic>Bam</italic>HI, <italic>Bcl</italic>I, <italic>Spe</italic>I and <italic>Xba</italic>I restriction sites are shown on insert C1.6. (D) Recovery rates [%] of cosmid pcosC1.6 and its truncated derivatives after selection in <italic>L. infantum</italic>. Promastigotes transfected with pcosC1.6 and any of the truncated variants (pcos-a to pcos-e, pcos210, pcos220) were mixed at equal ratio (C<sub>0</sub>). Two control cultures cultivated without Sb<sup>III</sup> for 12 days (C<sub>12</sub>) or 21 days (C<sub>21</sub>) were analysed along with the cultures selected at 500 μM Sb<sup>III</sup> for 12 days (S<sub>12</sub>) or at 400 μM Sb<sup>III</sup> for 21 days (S<sub>21</sub>). Episomes from surviving parasites were isolated and used for transformation of <italic>E. coli</italic>. From each transformation, the cosmid DNAs from 50 bacterial colonies were characterised by RFLA, and the share [%] of each cosmid type is displayed.</p></caption><graphic xlink:href="gr1"></graphic></fig><fig id="f0010"><label>Fig. 2</label><caption><p>(A) Dose–effect of antimonyl tartrate (Sb<sup>III</sup>) on the growth of <italic>L. braziliensis</italic> strains PER104 and PER002 transfected with cosmid pcosTL or pcosC1.6 respectively. Growth at 0 μM Sb<sup>III</sup> was defined as 100%. The dashed arrows indicate the 50% inhibiting concentration (IC<sub>50</sub>). Significance (IC<sub>50</sub>): <italic>p</italic> = 0.002, <italic>n</italic> = 6. (B) Effect of pcosC1.6 in <italic>L. infantum</italic>. Empty vector pcosTL and cosmid pcosC1.6 were transfected into <italic>L. infantum</italic> and selected under G418. Cells of both recombinant populations (5 × 10<sup>5</sup> cells ml<sup>−1</sup>) were grown under the indicated Sb<sup>III</sup> concentrations for 72 h. The diagram shows the cell density after 72 h relative to the control culture (0 μM Sb<sup>III</sup>). Numerical IC<sub>50</sub> values are indicated. Significance (IC<sub>50</sub>) <italic>p</italic> = 0.016, <italic>n</italic> = 5. (C) Constructs pcos-210, pcos-220, and the empty vector pcosTL were transfected into <italic>L. infantum</italic> and selected under G418. Cells of each recombinant population (5 × 10<sup>5</sup> cells ml<sup>−1</sup>) were challenged with the indicated Sb<sup>III</sup> concentrations for 72 h. The diagram shows the cell density after 72 h relative to the control culture (0 μM Sb<sup>III</sup>). The bars indicate the mean error. Significance (IC<sub>50</sub>) <italic>p</italic> = 0.008, <italic>n</italic> = 5. (D) Control of LbrM20.0210 expression by qPCR. Expression mediated by cosmid pcosC1.6 was given the value 1. Note that <italic>L. infantum</italic> expresses a homologous gene that is not amplified by the species-specific primers. Thus, the degree of overexpression cannot be determined. (E) Quantification of LbrM20.0210 expression in <italic>L. braziliensis</italic> strains PER002[pcosTL] and PER002cl7[pcosC1.6]. Expression in the control strain PER002cl7[pcosTL] was assigned the value 1. <italic>n</italic> = 6. The standard error of means is depicted.</p></caption><graphic xlink:href="gr2"></graphic></fig><fig id="f0015"><label>Fig. 3</label><caption><p>(A) Infection rate in bone marrow-derived macrophages under Sb<sup>V</sup> challenge. BMMs were infected with stationary growth phase <italic>L. infantum</italic> transfected either with vector pcosTL or with pcos-210. After removal of free parasites, the infected macrophages were incubated in the absence or presence of 160 μg ml<sup>−1</sup> Pentostam®. After 72 h, the cells were fixed with ice–cold methanol, stained with DAPI, and subjected to fluorescence microscopy. For each dataset, 100 macrophages were examined for the presence of parasites. Experiments were performed in quadruplicate and on separate days. The median infection rates are indicated by horizontal bars. Significance (*<italic>p</italic> = 0.029) was tested using the Mann–Whitney ranking test. <italic>n</italic> = 4. (B) Basic expression rate of ARM58 in two clinical isolates of <italic>L. braziliensis</italic>, PER002 (Sb<sup>III</sup> sensitive) and PER104 (Sb<sup>III</sup> resistant), measured by qPCR. Experiments were done in duplicate, arbitrary units. (C) ARM58 RNA expression in <italic>L. braziliensis</italic> populations under various selective pressure. Clone PER002cl7[pcos-210] was subjected to <italic>in vitro</italic> passage for 4 weeks with twice-weekly medium changes. The populations were kept without selection (2), under 50 μg ml<sup>−1</sup> G418 (3), under 3 μM Sb<sup>III</sup> (4), or under 10 μM Sb<sup>III</sup> (5). The PER002cl7 wild type was used for normalisation (1). Cultures were grown in duplicate, qPCR was done in duplicate for each culture (<italic>n</italic> = 4). The bars indicate the medians. Asterisks indicate significance (<sup>∗</sup><italic>p</italic> ⩽ 0.05).</p></caption><graphic xlink:href="gr3"></graphic></fig><fig id="f0020"><label>Fig. 4</label><caption><p>(A) ORF maps of the region around LbrM20.0210 for 5 <italic>Leishmania</italic> species and <italic>Trypanosoma brucei</italic>. (B) Phylogeny tree for LbrM20.0210 and LbrM20.0200. UPGMA algorithm, bootstrap analysis (1000 reps), uncorrected. Gene numbers are underlaid with colours red (for LbrM20.0210 orthologs) or yellow (LbrM20.0200 orthologs). (C) Domain structures for LbrM20.0210 and -0200. DUF = domain of unknown function. Domains are numbered sequentially in Roman numerals (I–IV) from N terminus to C terminus. Sequence conservation for each domain is indicated (<italic>I</italic> = identity, <italic>S</italic> = side chain similarity). Length markers in [amino acids] are given below. (D) Transmembrane domain prediction for LbrM20.0210 using the TMpred algorithm (<ext-link ext-link-type="uri" xlink:href="http://www.ch.embnet.org/software/TMPRED_form.html" id="ir0020">http://www.ch.embnet.org/software/TMPRED_form.html</ext-link>). Note the peak (score 792/819 i>o/o>i) corresponding to domain DUF1935-III and exceeding the threshold score of 500.</p></caption><graphic xlink:href="gr4"></graphic></fig><table-wrap id="t0005" position="float"><label>Table 1</label><caption><p>Outcomes for 6 independent selection screens.</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Selection</th><th>Acceptor strain</th><th>Donor strain</th><th>Sb<sup>III</sup> (μM)</th><th>Time (d)</th><th>Selected cosmids (%)</th><th>Chromosome/region</th></tr></thead><tbody><tr><td>S1.1</td><td>PER002</td><td>PER104</td><td align="char">25</td><td align="char">18</td><td>C1.6 (66)</td><td>20/903 984–946 647</td></tr><tr><td>S1.2</td><td>PER002</td><td>PER104</td><td align="char">90</td><td align="char">33</td><td>C1.6 (90)</td><td>20/903 984–946 647</td></tr><tr><td>S1.3</td><td>PER002</td><td>PER104</td><td align="char">90</td><td align="char">15</td><td>C1.6 (98)</td><td>20/903 984–946 647</td></tr><tr><td>S2.1</td><td>PER002</td><td>PER002</td><td align="char">75</td><td align="char">17</td><td>A3 (10)</td><td>20/913 015–951 701</td></tr><tr><td>S2.2</td><td>PER002</td><td>PER002</td><td align="char">75</td><td align="char">17</td><td>A3 (96)</td><td>20/913 015–951 701</td></tr><tr><td>S3</td><td><italic>L. peruviana</italic></td><td>PER104</td><td align="char">15</td><td align="char">30</td><td>B1 (40)</td><td>20/908 315–951 075</td></tr></tbody></table><table-wrap-foot><fn><p>Screens S1.1–S1.3 were performed using the Sb<sup>III</sup> sensitive strain PER002 and a cosmid library derived from the Sb<sup>III</sup> resistant strain PER104; screens S2.1.1 and S2.1.2 were consecutively performed using PER002 both as donor and acceptor, and screen 3 was performed using <italic>L. peruviana</italic> as receptor and strain PER104 as donor. Sb<sup>III</sup> concentrations (column 3) and selection time (column 4) varied depending on antimony batch variations. The dominant selected cosmids and their share of the overall recovered cosmids are given in column 5, while the corresponding chromosomal regions are given in column 6.</p></fn></table-wrap-foot></table-wrap></floats-group></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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