PLoS Neglected Tropical Diseases (Feb 2016)

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

  • 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

DOI
https://doi.org/10.1371/journal.pntd.0004403
Journal volume & issue
Vol. 10, no. 2
p. e0004403

Abstract

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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.