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What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira
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 c...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758666/ https://www.ncbi.nlm.nih.gov/pubmed/26890609 http://dx.doi.org/10.1371/journal.pntd.0004403 |
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author | Fouts, Derrick E. Matthias, Michael A. Adhikarla, Haritha Adler, Ben Amorim-Santos, Luciane Berg, Douglas E. Bulach, Dieter Buschiazzo, Alejandro Chang, Yung-Fu Galloway, Renee L. Haake, David A. Haft, Daniel H. Hartskeerl, Rudy Ko, Albert I. Levett, Paul N. Matsunaga, James Mechaly, Ariel E. Monk, Jonathan M. Nascimento, Ana L. T. Nelson, Karen E. Palsson, Bernhard Peacock, Sharon J. Picardeau, Mathieu Ricaldi, Jessica N. Thaipandungpanit, Janjira Wunder, Elsio A. Yang, X. Frank Zhang, Jun-Jie Vinetz, Joseph M. |
author_facet | Fouts, Derrick E. Matthias, Michael A. Adhikarla, Haritha Adler, Ben Amorim-Santos, Luciane Berg, Douglas E. Bulach, Dieter Buschiazzo, Alejandro Chang, Yung-Fu Galloway, Renee L. Haake, David A. Haft, Daniel H. Hartskeerl, Rudy Ko, Albert I. Levett, Paul N. Matsunaga, James Mechaly, Ariel E. Monk, Jonathan M. Nascimento, Ana L. T. Nelson, Karen E. Palsson, Bernhard Peacock, Sharon J. Picardeau, Mathieu Ricaldi, Jessica N. Thaipandungpanit, Janjira Wunder, Elsio A. Yang, X. Frank Zhang, Jun-Jie Vinetz, Joseph M. |
author_sort | Fouts, Derrick E. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4758666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47586662016-02-26 What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira Fouts, Derrick E. Matthias, Michael A. Adhikarla, Haritha Adler, Ben Amorim-Santos, Luciane Berg, Douglas E. Bulach, Dieter Buschiazzo, Alejandro Chang, Yung-Fu Galloway, Renee L. Haake, David A. Haft, Daniel H. Hartskeerl, Rudy Ko, Albert I. Levett, Paul N. Matsunaga, James Mechaly, Ariel E. Monk, Jonathan M. Nascimento, Ana L. T. Nelson, Karen E. Palsson, Bernhard Peacock, Sharon J. Picardeau, Mathieu Ricaldi, Jessica N. Thaipandungpanit, Janjira Wunder, Elsio A. Yang, X. Frank Zhang, Jun-Jie Vinetz, Joseph M. PLoS Negl Trop Dis Research Article 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. Public Library of Science 2016-02-18 /pmc/articles/PMC4758666/ /pubmed/26890609 http://dx.doi.org/10.1371/journal.pntd.0004403 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Fouts, Derrick E. Matthias, Michael A. Adhikarla, Haritha Adler, Ben Amorim-Santos, Luciane Berg, Douglas E. Bulach, Dieter Buschiazzo, Alejandro Chang, Yung-Fu Galloway, Renee L. Haake, David A. Haft, Daniel H. Hartskeerl, Rudy Ko, Albert I. Levett, Paul N. Matsunaga, James Mechaly, Ariel E. Monk, Jonathan M. Nascimento, Ana L. T. Nelson, Karen E. Palsson, Bernhard Peacock, Sharon J. Picardeau, Mathieu Ricaldi, Jessica N. Thaipandungpanit, Janjira Wunder, Elsio A. Yang, X. Frank Zhang, Jun-Jie Vinetz, Joseph M. What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira |
title | What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira |
title_full | What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira |
title_fullStr | What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira |
title_full_unstemmed | What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira |
title_short | What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira |
title_sort | what makes a bacterial species pathogenic?:comparative genomic analysis of the genus leptospira |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758666/ https://www.ncbi.nlm.nih.gov/pubmed/26890609 http://dx.doi.org/10.1371/journal.pntd.0004403 |
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