Evidence map›Paper›PMID 20061468›Full record

ArticleJournal of bacteriology2010

Genome sequence of the deep-rooted Yersinia pestis strain Angola reveals new insights into the evolution and pangenome of the plague bacterium.

Mark Eppinger, Patricia L Worsham, Mikeljon P Nikolich, David R Riley, Yinong Sebastian, Sherry Mou, Mark Achtman, Luther E Lindler, Jacques Ravel

Abstract read
In one paragraph

Article in Journal of bacteriology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

52 citing papers in PubMed.

  1. Article
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  3. Article
  4. Review
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  6. Review
  7. Zoonoses (Shannon, Ireland) · 2023
    Article
  8. Article
  9. Article
  10. Comparative Genomics ofMicroorganisms · 2022
    Article
  11. Genome Sequence Analysis and Characterization of Shiga Toxin 2 Production byFrontiers in cellular and infection microbiology · 2022
    Article
  12. Article
  13. Article
  14. Genetic and Virulence Profiles of EnteroaggregativeFrontiers in cellular and infection microbiology · 2020
    Article
  15. Pathogenomes of Atypical Non-shigatoxigenicFrontiers in microbiology · 2020
    Article
  16. Article
  17. AncientProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Mark EppingerInstitute for Genome Sciences and Department of Microbiology and Immunology, University of Maryland, School of Medicine, Baltimore, Maryland 21201, USA.
Patricia L Worsham
Mikeljon P Nikolich
David R Riley
Yinong Sebastian
Sherry Mou
Mark Achtman
Luther E Lindler
Jacques Ravel

Funding

NIAID NIH HHS N01 AI030071
6 · The paper itself

Abstract

To gain insights into the origin and genome evolution of the plague bacterium Yersinia pestis, we have sequenced the deep-rooted strain Angola, a virulent Pestoides isolate. Its ancient nature makes this atypical isolate of particular importance in understanding the evolution of plague pathogenicity. Its chromosome features a unique genetic make-up intermediate between modern Y. pestis isolates and its evolutionary ancestor, Y. pseudotuberculosis. Our genotypic and phenotypic analyses led us to conclude that Angola belongs to one of the most ancient Y. pestis lineages thus far sequenced. The mobilome carries the first reported chimeric plasmid combining the two species-specific virulence plasmids. Genomic findings were validated in virulence assays demonstrating that its pathogenic potential is distinct from modern Y. pestis isolates. Human infection with this particular isolate would not be diagnosed by the standard clinical tests, as Angola lacks the plasmid-borne capsule, and a possible emergence of this genotype raises major public health concerns. To assess the genomic plasticity in Y. pestis, we investigated the global gene reservoir and estimated the pangenome at 4,844 unique protein-coding genes. As shown by the genomic analysis of this evolutionary key isolate, we found that the genomic plasticity within Y. pestis clearly was not as limited as previously thought, which is strengthened by the detection of the largest number of isolate-specific single-nucleotide polymorphisms (SNPs) currently reported in the species. This study identified numerous novel genetic signatures, some of which seem to be intimately associated with plague virulence. These markers are valuable in the development of a robust typing system critical for forensic, diagnostic, and epidemiological studies.

Indexed as

Biological EvolutionGenome, BacterialAnimalsAntigens, BacterialBacterial ProteinsBase SequenceGene Expression Regulation, BacterialGenotypeGlobal HealthGuinea PigsMiceMice, Inbred BALB CPlaguePlasmidsVirulenceYersinia pestisAntigens, BacterialBacterial Proteins

Identifiers

PMID20061468
PMCPMC2832528

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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.