Antibacterial activity of extracellular compounds produced by a Pseudomonas strain against methicillin-resistant Staphylococcus aureus (MRSA) strains
Identifieur interne : 000F58 ( Main/Merge ); précédent : 000F57; suivant : 000F59Antibacterial activity of extracellular compounds produced by a Pseudomonas strain against methicillin-resistant Staphylococcus aureus (MRSA) strains
Auteurs : Viviane F. Cardozo [Brésil] ; Admilton G. Oliveira [Brésil] ; Erick K. Nishio [Brésil] ; Marcia Re Perugini [Brésil] ; Célia Gtj Andrade [Brésil] ; Wanderley D. Silveira [Brésil] ; Nelson Durán [Brésil] ; Galdino Andrade [Brésil] ; Renata Kt Kobayashi [Brésil] ; Gerson Nakazato [Brésil]Source :
- Annals of Clinical Microbiology and Antimicrobials [ 1476-0711 ] ; 2013.
Abstract
The emergence of multidrug-resistant bacteria is a world health problem.
Thirty clinical MRSA strains were isolated, and three standard MRSA strains were evaluated. The extracellular compounds were purified by vacuum liquid chromatography. Evaluation of antibacterial activity was performed by agar diffusion technique, determination of the minimal inhibitory concentration, curve of growth and viability and scanning electron microscopy. Interaction of an extracellular compound with silver nanoparticle was studied to evaluate antibacterial effect.
The F3 (ethyl acetate) and F3d (dichloromethane- ethyl acetate) fractions demonstrated antibacterial activity against the MRSA strains. Phenazine-1-carboxamide was identified and purified from the F3d fraction and demonstrated slight antibacterial activity against MRSA, and synergic effect when combined with silver nanoparticles produced by
These results suggest that
Url:
DOI: 10.1186/1476-0711-12-12
PubMed: 23773484
PubMed Central: 3695862
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Cardozo</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990</wicri:regionArea><wicri:noRegion>PR CP 86005-990</wicri:noRegion></affiliation></author><author><name sortKey="Oliveira, Admilton G" sort="Oliveira, Admilton G" uniqKey="Oliveira A" first="Admilton G" last="Oliveira">Admilton G. Oliveira</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990</wicri:regionArea><wicri:noRegion>PR CP 86005-990</wicri:noRegion></affiliation></author><author><name sortKey="Nishio, Erick K" sort="Nishio, Erick K" uniqKey="Nishio E" first="Erick K" last="Nishio">Erick K. Nishio</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990</wicri:regionArea><wicri:noRegion>PR CP 86005-990</wicri:noRegion></affiliation></author><author><name sortKey="Perugini, Marcia Re" sort="Perugini, Marcia Re" uniqKey="Perugini M" first="Marcia Re" last="Perugini">Marcia Re Perugini</name><affiliation wicri:level="1"><nlm:aff id="I2">Department of Pathology, Clinical Analysis and Toxicological, University of Londrina State, Londrina, PR CP 86038-440, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of Pathology, Clinical Analysis and Toxicological, University of Londrina State, Londrina, PR CP 86038-440</wicri:regionArea><wicri:noRegion>PR CP 86038-440</wicri:noRegion></affiliation></author><author><name sortKey="Andrade, Celia Gtj" sort="Andrade, Celia Gtj" uniqKey="Andrade C" first="Célia Gtj" last="Andrade">Célia Gtj Andrade</name><affiliation wicri:level="1"><nlm:aff id="I3">Department of General Biology, University of Londrina State, Londrina, PR CP 86051-990, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of General Biology, University of Londrina State, Londrina, PR CP 86051-990</wicri:regionArea><wicri:noRegion>PR CP 86051-990</wicri:noRegion></affiliation></author><author><name sortKey="Silveira, Wanderley D" sort="Silveira, Wanderley D" uniqKey="Silveira W" first="Wanderley D" last="Silveira">Wanderley D. Silveira</name><affiliation wicri:level="1"><nlm:aff id="I4">Department of Genetics, Evolution and Bioagent, Biology Institute, Campinas State University (UNICAMP), Campinas, SP CP 13083-970, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of Genetics, Evolution and Bioagent, Biology Institute, Campinas State University (UNICAMP), Campinas, SP CP 13083-970</wicri:regionArea><wicri:noRegion>SP CP 13083-970</wicri:noRegion></affiliation></author><author><name sortKey="Duran, Nelson" sort="Duran, Nelson" uniqKey="Duran N" first="Nelson" last="Durán">Nelson Durán</name><affiliation wicri:level="1"><nlm:aff id="I5">Department of Physical Chemistry, Chemistry Institute Campinas State University (UNICAMP), Campinas, SP CP 13083-970, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of Physical Chemistry, Chemistry Institute Campinas State University (UNICAMP), Campinas, SP CP 13083-970</wicri:regionArea><wicri:noRegion>SP CP 13083-970</wicri:noRegion></affiliation></author><author><name sortKey="Andrade, Galdino" sort="Andrade, Galdino" uniqKey="Andrade G" first="Galdino" last="Andrade">Galdino Andrade</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990</wicri:regionArea><wicri:noRegion>PR CP 86005-990</wicri:noRegion></affiliation></author><author><name sortKey="Kobayashi, Renata Kt" sort="Kobayashi, Renata Kt" uniqKey="Kobayashi R" first="Renata Kt" last="Kobayashi">Renata Kt Kobayashi</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990</wicri:regionArea><wicri:noRegion>PR CP 86005-990</wicri:noRegion></affiliation></author><author><name sortKey="Nakazato, Gerson" sort="Nakazato, Gerson" uniqKey="Nakazato G" first="Gerson" last="Nakazato">Gerson Nakazato</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990, Brazil</nlm:aff><country xml:lang="fr">Brésil</country><wicri:regionArea>Department of Microbiology, Biology Sciences Center, University of Londrina State, Londrina, PR CP 86005-990</wicri:regionArea><wicri:noRegion>PR CP 86005-990</wicri:noRegion></affiliation></author></analytic><series><title level="j">Annals of Clinical Microbiology and Antimicrobials</title><idno type="eISSN">1476-0711</idno><imprint><date when="2013">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Background</title><p>The emergence of multidrug-resistant bacteria is a world health problem. <italic>Staphylococcus aureus,</italic> including methicillin-resistant <italic>S. aureus</italic> (MRSA) strains, is one of the most important human pathogens associated with hospital and community-acquired infections. The aim of this work was to evaluate the antibacterial activity of a <italic>Pseudomonas aeruginosa</italic>-derived compound against MRSA strains.</p></sec><sec><title>Methods</title><p>Thirty clinical MRSA strains were isolated, and three standard MRSA strains were evaluated. The extracellular compounds were purified by vacuum liquid chromatography. Evaluation of antibacterial activity was performed by agar diffusion technique, determination of the minimal inhibitory concentration, curve of growth and viability and scanning electron microscopy. Interaction of an extracellular compound with silver nanoparticle was studied to evaluate antibacterial effect.</p></sec><sec><title>Results</title><p>The F3 (ethyl acetate) and F3d (dichloromethane- ethyl acetate) fractions demonstrated antibacterial activity against the MRSA strains. Phenazine-1-carboxamide was identified and purified from the F3d fraction and demonstrated slight antibacterial activity against MRSA, and synergic effect when combined with silver nanoparticles produced by <italic>Fusarium oxysporum</italic>. Organohalogen compound was purified from this fraction showing high antibacterial effect. Using scanning electron microscopy, we show that the F3d fraction caused morphological changes to the cell wall of the MRSA strains.</p></sec><sec><title>Conclusions</title><p>These results suggest that <italic>P. aeruginosa</italic>-produced compounds such as phenazines have inhibitory effects against MRSA and may be a good alternative treatment to control infections caused by MRSA.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Buke, C" uniqKey="Buke C">C Buke</name></author><author><name sortKey="Armand Lefevre, L" uniqKey="Armand Lefevre L">L Armand-Lefevre</name></author><author><name sortKey="Lolom, I" uniqKey="Lolom I">I Lolom</name></author><author><name sortKey="Guerinot, W" uniqKey="Guerinot W">W Guerinot</name></author><author><name sortKey="Deblangy, C" uniqKey="Deblangy C">C Deblangy</name></author><author><name sortKey="Ruimy, R" uniqKey="Ruimy R">R Ruimy</name></author><author><name sortKey="Andremont, A" 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sortKey="Wright, Pc" uniqKey="Wright P">PC Wright</name></author><author><name sortKey="Burgess, Jg" uniqKey="Burgess J">JG Burgess</name></author></analytic></biblStruct></listBibl></div1></back></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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