Evidence map›Paper›PMID 39018329›Full record

ArticlePLoS pathogens2024

Evolutionary insights into the emergence of virulent Leptospira spirochetes.

Alexandre Giraud-Gatineau, Cecilia Nieves, Luke B Harrison, Nadia Benaroudj, Frédéric J Veyrier, Mathieu Picardeau

Abstract read
In one paragraph

Article in PLoS pathogens, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed.

  1. Article
  2. Draft genome sequence ofMicrobiology resource announcements · 2026
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  5. Changing landscapes, shifting reservoirs: land-use change andApplied and environmental microbiology · 2026
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  6. TheInfection and immunity · 2026
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  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Host-Driven Genetic Diversity ofTransboundary and emerging diseases · 2026
    Article
  16. Article
  17. Article
  18. A Scoping Review of Antimicrobial Therapy inAnimals : an open access journal from MDPI · 2025
    Review
  19. Shaping the future ofJournal of medical microbiology · 2025
    Review
  20. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Alexandre Giraud-GatineauInstitut Pasteur, Université Paris Cité, Biology of Spirochetes Unit, Paris, France.
Cecilia NievesBacterial Symbionts Evolution, Centre Armand-Frappier Santé Biotechnologie, Institut National de la Recherche Scientifique, Université du Québec, Laval, Canada.
Luke B HarrisonBacterial Symbionts Evolution, Centre Armand-Frappier Santé Biotechnologie, Institut National de la Recherche Scientifique, Université du Québec, Laval, Canada.
Nadia BenaroudjInstitut Pasteur, Université Paris Cité, Biology of Spirochetes Unit, Paris, France.
Frédéric J VeyrierBacterial Symbionts Evolution, Centre Armand-Frappier Santé Biotechnologie, Institut National de la Recherche Scientifique, Université du Québec, Laval, Canada.
Mathieu PicardeauInstitut Pasteur, Université Paris Cité, Biology of Spirochetes Unit, Paris, France.ORCID 0000-0002-5338-5579

Funding

Virulence and Adaptation to the Host Environment of Pathogenic LeptospiraP01AI168148 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DAVID A HAAKE · 2023 to 2026
$11.8M
NIAID NIH HHS P01 AI168148
6 · The paper itself

Abstract

Pathogenic Leptospira are spirochete bacteria which cause leptospirosis, a re-emerging zoonotic disease of global importance. Here, we use a recently described lineage of environmental-adapted leptospires, which are evolutionarily the closest relatives of the highly virulent Leptospira species, to explore the key phenotypic traits and genetic determinants of Leptospira virulence. Through a comprehensive approach integrating phylogenomic comparisons with in vitro and in vivo phenotyping studies, we show that the evolution towards pathogenicity is associated with both a decrease of the ability to survive in the environment and the acquisition of strategies that enable successful host colonization. This includes the evasion of the mammalian complement system and the adaptations to avoid activation of the innate immune cells by the highly-virulent Leptospira species (also called P1+ species), unlike other species belonging to the phylogenetically related P1- and P2 groups, as well as saprophytes. Moreover, our analysis reveals specific genetic determinants that have undergone positive selection during the course of evolution in Leptospira, contributing directly to virulence and host adaptation as demonstrated by gain-of-function and knock-down studies. Taken together, our findings define a new vision on Leptospira pathogenicity, identifying virulence attributes associated with clinically relevant species, and provide insights into the evolution and emergence of these life-threatening pathogens.

Indexed as

LeptospiraLeptospirosisPhylogenyAnimalsBiological EvolutionEvolution, MolecularHumansMiceVirulence

Identifiers

PMID39018329
PMCPMC11285912

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.