Evidence map›Paper›PMID 19103769›Full record

ArticleInfection and immunity2009

The Yersinia pestis caf1M1A1 fimbrial capsule operon promotes transmission by flea bite in a mouse model of bubonic plague.

Florent Sebbane, Clayton Jarrett, Donald Gardner, Daniel Long, B Joseph Hinnebusch

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 79 citations in OpenAlex.

  1. Emergence, global dispersal, and local adaptations ofApplied and environmental microbiology · 2026
    Review
  2. Article
  3. Molecular turn inEmerging microbes & infections · 2025
    Article
  4. Article
  5. Multiplex PCR System for the Diagnosis of Plague.Current molecular medicine · 2025
    Review
  6. Review
  7. Article
  8. Zoonoses (Shannon, Ireland) · 2023
    Article
  9. Article
  10. Emergence and spread of ancestralProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Article
  12. Deletion of Yersinia pestisJournal of bacteriology · 2021
    Article
  13. Review
  14. Biomolecules · 2020
    Review
  15. Article
  16. Development of Anti-ImmunoTargets and therapy · 2020
    Article
  17. 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

5 authors at 2 institutions in 2 countries.

Florent SebbaneInstitut National de la Santé et de la Recherche Médicale, U801, Institut Pasteur de Lille, Lille, France. florent.sebbane@ibl.fr
Clayton Jarrett
Donald Gardner
Daniel Long
B Joseph Hinnebusch
National Institute of Allergy and Infectious Diseases · USInstitut Pasteur de Lille · FR

Funding

Transmission Of Yersinia Pestis By Fleas: Molecular MechanismsZIAAI000796 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HINNEBUSCH, B J · 2009 to 2023
$9.7M
Transmission-Yersinia Pestis Fleas: Molecular MechanismZ01AI000796 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI HINNEBUSCH, B J · 1997 to 2008
$1.1M
Intramural NIH HHS
6 · The paper itself

Abstract

Plague is a zoonosis transmitted by fleas and caused by the gram-negative bacterium Yersinia pestis. During infection, the plasmidic caf1M1A1 operon that encodes the Y. pestis F1 protein capsule is highly expressed, and anti-F1 antibodies are protective. Surprisingly, the capsule is not required for virulence after injection of cultured bacteria, even though it is an antiphagocytic factor and capsule-deficient Y. pestis strains are rarely isolated. We found that a caf-negative Y. pestis mutant was not impaired in either flea colonization or virulence in mice after intradermal inoculation of cultured bacteria. In contrast, absence of the caf operon decreased bubonic plague incidence after a flea bite. Successful development of plague in mice infected by flea bite with the caf-negative mutant required a higher number of infective bites per challenge. In addition, the mutant displayed a highly autoaggregative phenotype in infected liver and spleen. The results suggest that acquisition of the caf locus via horizontal transfer by an ancestral Y. pestis strain increased transmissibility and the potential for epidemic spread. In addition, our data support a model in which atypical caf-negative strains could emerge during climatic conditions that favor a high flea burden. Human infection with such strains would not be diagnosed by the standard clinical tests that detect F1 antibody or antigen, suggesting that more comprehensive surveillance for atypical Y. pestis strains in plague foci may be necessary. The results also highlight the importance of studying Y. pestis pathogenesis in the natural context of arthropod-borne transmission.

Indexed as

AnimalsBacterial ProteinsDisease Models, AnimalFimbriae ProteinsInsect Bites and StingsMiceMutationOperonPlagueSiphonapteraVirulenceYersinia pestisBacterial Proteinscaf1 protein, Yersinia pestisFimbriae Proteins

Identifiers

PMID19103769
PMCPMC2643634
OpenAlexW2154275726

What OpenQuestion holds

Textmetadata
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.