Evidence map›Paper›PMID 31026256›Full record

ArticlePLoS neglected tropical diseases2019

Genus-wide Leptospira core genome multilocus sequence typing for strain taxonomy and global surveillance.

Julien Guglielmini, Pascale Bourhy, Olivier Schiettekatte, Farida Zinini, Sylvain Brisse, Mathieu Picardeau

Erratum issuedAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 101 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 1 pooled it
–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

101 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Prevalence ofFrontiers in veterinary science · 2022
    Pooled it
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  5. Review
  6. Retrospective Molecular Detection and Characterization of PathogenicTropical medicine and infectious disease · 2026
    Article
  7. Molecular epidemiology of rodent-borneJournal of medical microbiology · 2026
    Article
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  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Host-Driven Genetic Diversity ofTransboundary and emerging diseases · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Shaping the future ofJournal of medical microbiology · 2025
    Review
  19. Article
  20. Leptospirosis.Nature reviews. Disease primers · 2025
    Review

41 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Julien GuglielminiInstitut Pasteur, Bioinformatics and Biostatistics Hub, C3BI, USR 3756 IP CNRS, Paris, France.
Pascale BourhyInstitut Pasteur, Biology of Spirochetes unit, National Reference Center for Leptospirosis, Paris, France.
Olivier SchiettekatteInstitut Pasteur, Biology of Spirochetes unit, National Reference Center for Leptospirosis, Paris, France.
Farida ZininiInstitut Pasteur, Biology of Spirochetes unit, National Reference Center for Leptospirosis, Paris, France.
Sylvain BrisseInstitut Pasteur, Biodiversity and Epidemiology of Bacterial Pathogens, Paris, France.
Mathieu PicardeauInstitut Pasteur, Biology of Spirochetes unit, National Reference Center for Leptospirosis, Paris, France.ORCID 0000-0002-5338-5579

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leptospira is a highly heterogeneous bacterial genus that can be divided into three evolutionary lineages and >300 serovars. The causative agents of leptospirosis are responsible of an emerging zoonotic disease worldwide. To advance our understanding of the biodiversity of Leptospira strains at the global level, we evaluated the performance of whole-genome sequencing (WGS) as a genus-wide strain classification and genotyping tool. Herein we propose a set of 545 highly conserved loci as a core genome MLST (cgMLST) genotyping scheme applicable to the entire Leptospira genus, including non-pathogenic species. Evaluation of cgMLST genotyping was undertaken with 509 genomes, including 327 newly sequenced genomes, from diverse species, sources and geographical locations. Phylogenetic analysis showed that cgMLST defines species, clades, subclades, clonal groups and cgMLST sequence types (cgST), with high precision and robustness to missing data. Novel Leptospira species, including a novel subclade named S2 (saprophytes 2), were identified. We defined clonal groups (CG) optimally using a single-linkage clustering threshold of 40 allelic mismatches. While some CGs such as L. interrogans CG6 (serogroup Icterohaemorrhagiae) are globally distributed, others are geographically restricted. cgMLST was congruent with classical MLST schemes, but had greatly improved resolution and broader applicability. Single nucleotide polymorphisms within single cgST groups was limited to <30 SNPs, underlining a potential role for cgMLST in epidemiological surveillance. Finally, cgMLST allowed identification of serogroups and closely related serovars. In conclusion, the proposed cgMLST strategy allows high-resolution genotyping of Leptospira isolates across the phylogenetic breadth of the genus. The unified genomic taxonomy of Leptospira strains, available publicly at http://bigsdb.pasteur.fr/leptospira, will facilitate global harmonization of Leptospira genotyping, strain emergence follow-up and novel collaborative studies of the epidemiology and evolution of this emerging pathogen.

Indexed as

AnimalsDisease OutbreaksEnvironmentGenome, BacterialGenotypeHumansLeptospiraLeptospirosisMultilocus Sequence TypingPhylogenySerogroupWhole Genome Sequencing

Identifiers

PMID31026256
PMCPMC6513109

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Registered trials

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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 OpenQuestion graph.