Evidence map›Paper›PMID 24675805›Full record

ArticlePLoS pathogens2014

New insights into how Yersinia pestis adapts to its mammalian host during bubonic plague.

Elizabeth Pradel, Nadine Lemaître, Maud Merchez, Isabelle Ricard, Angéline Reboul, Amélie Dewitte, Florent Sebbane

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.9field-weighted citation impact, top 5% of its field
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

42 citing papers in PubMed, 57 citations in OpenAlex.

  1. Pseudogenization of the cntQ permease confers distinct yersinopine-metal uptake selectivity in Yersinia species.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
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  3. Emergence, global dispersal, and local adaptations ofApplied and environmental microbiology · 2026
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  6. Assessing the threat ofAntimicrobial agents and chemotherapy · 2025
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  11. Emergence and spread of ancestralProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Stone AgeProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Yersinia pestis antibiotic resistance: a systematic review.Osong public health and research perspectives · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Living with plague: Lessons from the Soviet Union's antiplague system.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  20. Review
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

7 authors at 4 institutions in 1 country.

Elizabeth PradelEquipe Peste et Yersinia pestis; INSERM U1019, Lille, France; Centre National de la Recherche Scientifique UMR8204, Lille, France; Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France; Univ Lille Nord de France, Lille, France; UDSL, Centre d'Infection et d'Immunité de Lille, Lille, France.
Nadine LemaîtreEquipe Peste et Yersinia pestis; INSERM U1019, Lille, France; Centre National de la Recherche Scientifique UMR8204, Lille, France; Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France; Univ Lille Nord de France, Lille, France; UDSL, Centre d'Infection et d'Immunité de Lille, Lille, France; CHU Lille, Lille, France.
Maud MerchezEquipe Peste et Yersinia pestis; INSERM U1019, Lille, France; Centre National de la Recherche Scientifique UMR8204, Lille, France; Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France; Univ Lille Nord de France, Lille, France; UDSL, Centre d'Infection et d'Immunité de Lille, Lille, France.
Isabelle RicardEquipe Peste et Yersinia pestis; INSERM U1019, Lille, France; Centre National de la Recherche Scientifique UMR8204, Lille, France; Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France; Univ Lille Nord de France, Lille, France; UDSL, Centre d'Infection et d'Immunité de Lille, Lille, France.
Angéline ReboulEquipe Peste et Yersinia pestis; INSERM U1019, Lille, France; Centre National de la Recherche Scientifique UMR8204, Lille, France; Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France; Univ Lille Nord de France, Lille, France; UDSL, Centre d'Infection et d'Immunité de Lille, Lille, France.
Amélie DewitteEquipe Peste et Yersinia pestis; INSERM U1019, Lille, France; Centre National de la Recherche Scientifique UMR8204, Lille, France; Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France; Univ Lille Nord de France, Lille, France; UDSL, Centre d'Infection et d'Immunité de Lille, Lille, France.
Florent SebbaneEquipe Peste et Yersinia pestis; INSERM U1019, Lille, France; Centre National de la Recherche Scientifique UMR8204, Lille, France; Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France; Univ Lille Nord de France, Lille, France; UDSL, Centre d'Infection et d'Immunité de Lille, Lille, France.
Inserm · FRInstitut Pasteur de Lille · FRUniversité Lille Nord de France · FRUniversité de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bubonic plague (a fatal, flea-transmitted disease) remains an international public health concern. Although our understanding of the pathogenesis of bubonic plague has improved significantly over the last few decades, researchers have still not been able to define the complete set of Y. pestis genes needed for disease or to characterize the mechanisms that enable infection. Here, we generated a library of Y. pestis mutants, each lacking one or more of the genes previously identified as being up-regulated in vivo. We then screened the library for attenuated virulence in rodent models of bubonic plague. Importantly, we tested mutants both individually and using a novel, "per-pool" screening method that we have developed. Our data showed that in addition to genes involved in physiological adaptation and resistance to the stress generated by the host, several previously uncharacterized genes are required for virulence. One of these genes (ympt1.66c, which encodes a putative helicase) has been acquired by horizontal gene transfer. Deletion of ympt1.66c reduced Y. pestis' ability to spread to the lymph nodes draining the dermal inoculation site--probably because loss of this gene decreased the bacteria's ability to survive inside macrophages. Our results suggest that (i) intracellular survival during the early stage of infection is important for plague and (ii) horizontal gene transfer was crucial in the acquisition of this ability.

Indexed as

AnimalsDisease Models, AnimalFemaleHost-Parasite InteractionsHumansMacrophagesPlagueRatsVirulenceYersinia pestis

Identifiers

PMID24675805
PMCPMC3968184
OpenAlexW2149219044

What OpenQuestion 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 OpenQuestion graph.