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What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira.

Identifieur interne : 002291 ( PubMed/Corpus ); précédent : 002290; suivant : 002292

What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira.

Auteurs : Derrick E. Fouts ; Michael A. Matthias ; Haritha Adhikarla ; Ben Adler ; Luciane Amorim-Santos ; Douglas E. Berg ; Dieter Bulach ; Alejandro Buschiazzo ; Yung-Fu Chang ; Renee L. Galloway ; David A. Haake ; Daniel H. Haft ; Rudy Hartskeerl ; Albert I. Ko ; Paul N. Levett ; James Matsunaga ; Ariel E. Mechaly ; Jonathan M. Monk ; Ana L T. Nascimento ; Karen E. Nelson ; Bernhard Palsson ; Sharon J. Peacock ; Mathieu Picardeau ; Jessica N. Ricaldi ; Janjira Thaipandungpanit ; Elsio A. Wunder ; X Frank Yang ; Jun-Jie Zhang ; Joseph M. Vinetz

Source :

RBID : pubmed:26890609

English descriptors

Abstract

Leptospirosis, caused by spirochetes of the genus Leptospira, is a globally widespread, neglected and emerging zoonotic disease. While whole genome analysis of individual pathogenic, intermediately pathogenic and saprophytic Leptospira species has been reported, comprehensive cross-species genomic comparison of all known species of infectious and non-infectious Leptospira, with the goal of identifying genes related to pathogenesis and mammalian host adaptation, remains a key gap in the field. Infectious Leptospira, comprised of pathogenic and intermediately pathogenic Leptospira, evolutionarily diverged from non-infectious, saprophytic Leptospira, as demonstrated by the following computational biology analyses: 1) the definitive taxonomy and evolutionary relatedness among all known Leptospira species; 2) genomically-predicted metabolic reconstructions that indicate novel adaptation of infectious Leptospira to mammals, including sialic acid biosynthesis, pathogen-specific porphyrin metabolism and the first-time demonstration of cobalamin (B12) autotrophy as a bacterial virulence factor; 3) CRISPR/Cas systems demonstrated only to be present in pathogenic Leptospira, suggesting a potential mechanism for this clade's refractoriness to gene targeting; 4) finding Leptospira pathogen-specific specialized protein secretion systems; 5) novel virulence-related genes/gene families such as the Virulence Modifying (VM) (PF07598 paralogs) proteins and pathogen-specific adhesins; 6) discovery of novel, pathogen-specific protein modification and secretion mechanisms including unique lipoprotein signal peptide motifs, Sec-independent twin arginine protein secretion motifs, and the absence of certain canonical signal recognition particle proteins from all Leptospira; and 7) and demonstration of infectious Leptospira-specific signal-responsive gene expression, motility and chemotaxis systems. By identifying large scale changes in infectious (pathogenic and intermediately pathogenic) vs. non-infectious Leptospira, this work provides new insights into the evolution of a genus of bacterial pathogens. This work will be a comprehensive roadmap for understanding leptospirosis pathogenesis. More generally, it provides new insights into mechanisms by which bacterial pathogens adapt to mammalian hosts.

DOI: 10.1371/journal.pntd.0004403
PubMed: 26890609

Links to Exploration step

pubmed:26890609

Le document en format XML

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<name sortKey="Galloway, Renee L" sort="Galloway, Renee L" uniqKey="Galloway R" first="Renee L" last="Galloway">Renee L. Galloway</name>
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<name sortKey="Haake, David A" sort="Haake, David A" uniqKey="Haake D" first="David A" last="Haake">David A. Haake</name>
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<name sortKey="Haft, Daniel H" sort="Haft, Daniel H" uniqKey="Haft D" first="Daniel H" last="Haft">Daniel H. Haft</name>
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<name sortKey="Hartskeerl, Rudy" sort="Hartskeerl, Rudy" uniqKey="Hartskeerl R" first="Rudy" last="Hartskeerl">Rudy Hartskeerl</name>
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<name sortKey="Ko, Albert I" sort="Ko, Albert I" uniqKey="Ko A" first="Albert I" last="Ko">Albert I. Ko</name>
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<name sortKey="Levett, Paul N" sort="Levett, Paul N" uniqKey="Levett P" first="Paul N" last="Levett">Paul N. Levett</name>
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<name sortKey="Thaipandungpanit, Janjira" sort="Thaipandungpanit, Janjira" uniqKey="Thaipandungpanit J" first="Janjira" last="Thaipandungpanit">Janjira Thaipandungpanit</name>
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<name sortKey="Wunder, Elsio A" sort="Wunder, Elsio A" uniqKey="Wunder E" first="Elsio A" last="Wunder">Elsio A. Wunder</name>
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<name sortKey="Yang, X Frank" sort="Yang, X Frank" uniqKey="Yang X" first="X Frank" last="Yang">X Frank Yang</name>
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<nlm:affiliation>Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.</nlm:affiliation>
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<name sortKey="Zhang, Jun Jie" sort="Zhang, Jun Jie" uniqKey="Zhang J" first="Jun-Jie" last="Zhang">Jun-Jie Zhang</name>
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<nlm:affiliation>Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.</nlm:affiliation>
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<name sortKey="Vinetz, Joseph M" sort="Vinetz, Joseph M" uniqKey="Vinetz J" first="Joseph M" last="Vinetz">Joseph M. Vinetz</name>
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</affiliation>
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<author>
<name sortKey="Amorim Santos, Luciane" sort="Amorim Santos, Luciane" uniqKey="Amorim Santos L" first="Luciane" last="Amorim-Santos">Luciane Amorim-Santos</name>
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<nlm:affiliation>Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.</nlm:affiliation>
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<name sortKey="Berg, Douglas E" sort="Berg, Douglas E" uniqKey="Berg D" first="Douglas E" last="Berg">Douglas E. Berg</name>
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<name sortKey="Bulach, Dieter" sort="Bulach, Dieter" uniqKey="Bulach D" first="Dieter" last="Bulach">Dieter Bulach</name>
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<nlm:affiliation>Victorian Bioinformatics Consortium, Monash University, Clayton, Victoria, Australia.</nlm:affiliation>
</affiliation>
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<name sortKey="Buschiazzo, Alejandro" sort="Buschiazzo, Alejandro" uniqKey="Buschiazzo A" first="Alejandro" last="Buschiazzo">Alejandro Buschiazzo</name>
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<nlm:affiliation>Institut Pasteur de Montevideo, Laboratory of Molecular and Structural Microbiology, Montevideo, Uruguay.</nlm:affiliation>
</affiliation>
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<author>
<name sortKey="Chang, Yung Fu" sort="Chang, Yung Fu" uniqKey="Chang Y" first="Yung-Fu" last="Chang">Yung-Fu Chang</name>
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<nlm:affiliation>Department of Population Medicine & Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Galloway, Renee L" sort="Galloway, Renee L" uniqKey="Galloway R" first="Renee L" last="Galloway">Renee L. Galloway</name>
<affiliation>
<nlm:affiliation>Centers for Disease Control and Prevention (DHHS, CDC, OID, NCEZID, DHCPP, BSPB), Atlanta, Georgia, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Haake, David A" sort="Haake, David A" uniqKey="Haake D" first="David A" last="Haake">David A. Haake</name>
<affiliation>
<nlm:affiliation>VA Greater Los Angeles Healthcare System, Los Angeles, California, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Haft, Daniel H" sort="Haft, Daniel H" uniqKey="Haft D" first="Daniel H" last="Haft">Daniel H. Haft</name>
<affiliation>
<nlm:affiliation>J. Craig Venter Institute, Rockville, Maryland, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Hartskeerl, Rudy" sort="Hartskeerl, Rudy" uniqKey="Hartskeerl R" first="Rudy" last="Hartskeerl">Rudy Hartskeerl</name>
<affiliation>
<nlm:affiliation>WHO/FAO/OIE and National Collaborating Centre for Reference and Research on Leptospirosis, KIT Biomedical Research, Royal Tropical Institute (KIT), Amsterdam, The Netherlands.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Ko, Albert I" sort="Ko, Albert I" uniqKey="Ko A" first="Albert I" last="Ko">Albert I. Ko</name>
<affiliation>
<nlm:affiliation>Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Levett, Paul N" sort="Levett, Paul N" uniqKey="Levett P" first="Paul N" last="Levett">Paul N. Levett</name>
<affiliation>
<nlm:affiliation>Government of Saskatchewan, Disease Control Laboratory Regina, Canada.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Matsunaga, James" sort="Matsunaga, James" uniqKey="Matsunaga J" first="James" last="Matsunaga">James Matsunaga</name>
<affiliation>
<nlm:affiliation>VA Greater Los Angeles Healthcare System, Los Angeles, California, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Mechaly, Ariel E" sort="Mechaly, Ariel E" uniqKey="Mechaly A" first="Ariel E" last="Mechaly">Ariel E. Mechaly</name>
<affiliation>
<nlm:affiliation>Institut Pasteur de Montevideo, Laboratory of Molecular and Structural Microbiology, Montevideo, Uruguay.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Monk, Jonathan M" sort="Monk, Jonathan M" uniqKey="Monk J" first="Jonathan M" last="Monk">Jonathan M. Monk</name>
<affiliation>
<nlm:affiliation>Department of Bioengineering, University of California, San Diego, La Jolla, California, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Nascimento, Ana L T" sort="Nascimento, Ana L T" uniqKey="Nascimento A" first="Ana L T" last="Nascimento">Ana L T. Nascimento</name>
<affiliation>
<nlm:affiliation>Centro de Biotecnologia, Instituto Butantan, São Paulo, SP, Brazil.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Nelson, Karen E" sort="Nelson, Karen E" uniqKey="Nelson K" first="Karen E" last="Nelson">Karen E. Nelson</name>
<affiliation>
<nlm:affiliation>J. Craig Venter Institute, Rockville, Maryland, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Palsson, Bernhard" sort="Palsson, Bernhard" uniqKey="Palsson B" first="Bernhard" last="Palsson">Bernhard Palsson</name>
<affiliation>
<nlm:affiliation>Department of Bioengineering, University of California, San Diego, La Jolla, California, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Peacock, Sharon J" sort="Peacock, Sharon J" uniqKey="Peacock S" first="Sharon J" last="Peacock">Sharon J. Peacock</name>
<affiliation>
<nlm:affiliation>Department of Medicine, University of Cambridge, Cambridge, United Kingdom.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Picardeau, Mathieu" sort="Picardeau, Mathieu" uniqKey="Picardeau M" first="Mathieu" last="Picardeau">Mathieu Picardeau</name>
<affiliation>
<nlm:affiliation>Institut Pasteur, Biology of Spirochetes Unit, National Reference Centre and WHO Collaborating Center for Leptospirosis, Paris, France.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Ricaldi, Jessica N" sort="Ricaldi, Jessica N" uniqKey="Ricaldi J" first="Jessica N" last="Ricaldi">Jessica N. Ricaldi</name>
<affiliation>
<nlm:affiliation>Instituto de Medicina Tropical Alexander von Humboldt; Facultad de Medicina Alberto Hurtado, Universidd Peruana Cayetano Heredia, Lima, Peru.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Thaipandungpanit, Janjira" sort="Thaipandungpanit, Janjira" uniqKey="Thaipandungpanit J" first="Janjira" last="Thaipandungpanit">Janjira Thaipandungpanit</name>
<affiliation>
<nlm:affiliation>Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Wunder, Elsio A" sort="Wunder, Elsio A" uniqKey="Wunder E" first="Elsio A" last="Wunder">Elsio A. Wunder</name>
<affiliation>
<nlm:affiliation>Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Yang, X Frank" sort="Yang, X Frank" uniqKey="Yang X" first="X Frank" last="Yang">X Frank Yang</name>
<affiliation>
<nlm:affiliation>Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Zhang, Jun Jie" sort="Zhang, Jun Jie" uniqKey="Zhang J" first="Jun-Jie" last="Zhang">Jun-Jie Zhang</name>
<affiliation>
<nlm:affiliation>Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Vinetz, Joseph M" sort="Vinetz, Joseph M" uniqKey="Vinetz J" first="Joseph M" last="Vinetz">Joseph M. Vinetz</name>
<affiliation>
<nlm:affiliation>Division of Infectious Diseases, Department of Medicine, University of California San Diego School of Medicine, La Jolla, California, United States of America.</nlm:affiliation>
</affiliation>
</author>
</analytic>
<series>
<title level="j">PLoS neglected tropical diseases</title>
<idno type="eISSN">1935-2735</idno>
<imprint>
<date when="2016" type="published">2016</date>
</imprint>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Animals</term>
<term>Bacterial Proteins (genetics)</term>
<term>Bacterial Proteins (metabolism)</term>
<term>Bacterial Secretion Systems</term>
<term>Base Sequence</term>
<term>Evolution, Molecular</term>
<term>Genome, Bacterial</term>
<term>Genomics</term>
<term>Humans</term>
<term>Leptospira (classification)</term>
<term>Leptospira (genetics)</term>
<term>Leptospira (isolation & purification)</term>
<term>Leptospira (pathogenicity)</term>
<term>Leptospirosis (microbiology)</term>
<term>Leptospirosis (veterinary)</term>
<term>Molecular Sequence Data</term>
<term>Phylogeny</term>
<term>Protein Sorting Signals</term>
<term>Virulence</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Bacterial Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Bacterial Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="classification" xml:lang="en">
<term>Leptospira</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Leptospira</term>
</keywords>
<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en">
<term>Leptospira</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Leptospirosis</term>
</keywords>
<keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en">
<term>Leptospira</term>
</keywords>
<keywords scheme="MESH" qualifier="veterinary" xml:lang="en">
<term>Leptospirosis</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Bacterial Secretion Systems</term>
<term>Base Sequence</term>
<term>Evolution, Molecular</term>
<term>Genome, Bacterial</term>
<term>Genomics</term>
<term>Humans</term>
<term>Molecular Sequence Data</term>
<term>Phylogeny</term>
<term>Protein Sorting Signals</term>
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<front>
<div type="abstract" xml:lang="en">Leptospirosis, caused by spirochetes of the genus Leptospira, is a globally widespread, neglected and emerging zoonotic disease. While whole genome analysis of individual pathogenic, intermediately pathogenic and saprophytic Leptospira species has been reported, comprehensive cross-species genomic comparison of all known species of infectious and non-infectious Leptospira, with the goal of identifying genes related to pathogenesis and mammalian host adaptation, remains a key gap in the field. Infectious Leptospira, comprised of pathogenic and intermediately pathogenic Leptospira, evolutionarily diverged from non-infectious, saprophytic Leptospira, as demonstrated by the following computational biology analyses: 1) the definitive taxonomy and evolutionary relatedness among all known Leptospira species; 2) genomically-predicted metabolic reconstructions that indicate novel adaptation of infectious Leptospira to mammals, including sialic acid biosynthesis, pathogen-specific porphyrin metabolism and the first-time demonstration of cobalamin (B12) autotrophy as a bacterial virulence factor; 3) CRISPR/Cas systems demonstrated only to be present in pathogenic Leptospira, suggesting a potential mechanism for this clade's refractoriness to gene targeting; 4) finding Leptospira pathogen-specific specialized protein secretion systems; 5) novel virulence-related genes/gene families such as the Virulence Modifying (VM) (PF07598 paralogs) proteins and pathogen-specific adhesins; 6) discovery of novel, pathogen-specific protein modification and secretion mechanisms including unique lipoprotein signal peptide motifs, Sec-independent twin arginine protein secretion motifs, and the absence of certain canonical signal recognition particle proteins from all Leptospira; and 7) and demonstration of infectious Leptospira-specific signal-responsive gene expression, motility and chemotaxis systems. By identifying large scale changes in infectious (pathogenic and intermediately pathogenic) vs. non-infectious Leptospira, this work provides new insights into the evolution of a genus of bacterial pathogens. This work will be a comprehensive roadmap for understanding leptospirosis pathogenesis. More generally, it provides new insights into mechanisms by which bacterial pathogens adapt to mammalian hosts.</div>
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<Title>PLoS neglected tropical diseases</Title>
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<AbstractText>Leptospirosis, caused by spirochetes of the genus Leptospira, is a globally widespread, neglected and emerging zoonotic disease. While whole genome analysis of individual pathogenic, intermediately pathogenic and saprophytic Leptospira species has been reported, comprehensive cross-species genomic comparison of all known species of infectious and non-infectious Leptospira, with the goal of identifying genes related to pathogenesis and mammalian host adaptation, remains a key gap in the field. Infectious Leptospira, comprised of pathogenic and intermediately pathogenic Leptospira, evolutionarily diverged from non-infectious, saprophytic Leptospira, as demonstrated by the following computational biology analyses: 1) the definitive taxonomy and evolutionary relatedness among all known Leptospira species; 2) genomically-predicted metabolic reconstructions that indicate novel adaptation of infectious Leptospira to mammals, including sialic acid biosynthesis, pathogen-specific porphyrin metabolism and the first-time demonstration of cobalamin (B12) autotrophy as a bacterial virulence factor; 3) CRISPR/Cas systems demonstrated only to be present in pathogenic Leptospira, suggesting a potential mechanism for this clade's refractoriness to gene targeting; 4) finding Leptospira pathogen-specific specialized protein secretion systems; 5) novel virulence-related genes/gene families such as the Virulence Modifying (VM) (PF07598 paralogs) proteins and pathogen-specific adhesins; 6) discovery of novel, pathogen-specific protein modification and secretion mechanisms including unique lipoprotein signal peptide motifs, Sec-independent twin arginine protein secretion motifs, and the absence of certain canonical signal recognition particle proteins from all Leptospira; and 7) and demonstration of infectious Leptospira-specific signal-responsive gene expression, motility and chemotaxis systems. By identifying large scale changes in infectious (pathogenic and intermediately pathogenic) vs. non-infectious Leptospira, this work provides new insights into the evolution of a genus of bacterial pathogens. This work will be a comprehensive roadmap for understanding leptospirosis pathogenesis. More generally, it provides new insights into mechanisms by which bacterial pathogens adapt to mammalian hosts.</AbstractText>
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<DescriptorName UI="D001426" MajorTopicYN="N">Bacterial Proteins</DescriptorName>
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<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
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<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<DescriptorName UI="D007919" MajorTopicYN="N">Leptospira</DescriptorName>
<QualifierName UI="Q000145" MajorTopicYN="N">classification</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
<QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D007922" MajorTopicYN="N">Leptospirosis</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
<QualifierName UI="Q000662" MajorTopicYN="Y">veterinary</QualifierName>
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<DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D021382" MajorTopicYN="N">Protein Sorting Signals</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D014774" MajorTopicYN="N">Virulence</DescriptorName>
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