Evidence map›Paper›PMID 18453279›Full record

ReviewCurrent topics in microbiology and immunology2008

Yersinia pestis biofilm in the flea vector and its role in the transmission of plague.

B J Hinnebusch, D L Erickson

Open access · greenAbstract readReview
In one paragraph

Review in Current topics in microbiology and immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
28.3field-weighted citation impact, top 1% 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

71 citing papers in PubMed, 128 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Infection and immunity · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. The RNA chaperone Hfq has a multifaceted role inFrontiers in cellular and infection microbiology · 2024
    Article
  11. Article
  12. Article
  13. Genomic Analysis ofPathogens (Basel, Switzerland) · 2023
    Article
  14. Review
  15. Article
  16. A frameshift ineLife · 2023
    Article
  17. Article
  18. Stone AgeProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Article
  20. Review

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

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

2 authors at 1 institution in 1 country.

B J HinnebuschLaboratory of Zoonotic Pathogens, Rocky Mountain Laboratories, NIH, NIAID, Hamilton, MT 59840, USA. jhinnebusch@niaid.nih.gov
D L Erickson
Rocky Mountain Biological Laboratory · US

Funding

Animal Models to Study Plague Infection and ImmunityZIAAI000919 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HINNEBUSCH, B J · 2009 to 2023
$8.3M
Transmission-Yersinia Pestis Fleas: Molecular MechanismZ01AI000796 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI HINNEBUSCH, B J · 1997 to 2008
$1.1M
Intramural NIH HHS Z01 AI000796Intramural NIH HHS ZIA AI000919
6 · The paper itself

Abstract

Transmission by fleabite is a relatively recent evolutionary adaptation of Yersinia pestis, the bacterial agent of bubonic plague. To produce a transmissible infection, Y. pestis grows as an attached biofilm in the foregut of the flea vector. Biofilm formation both in the flea foregut and in vitro is dependent on an extracellular matrix (ECM) synthesized by the Yersinia hms gene products. The hms genes are similar to the pga and ica genes of Escherichia coli and Staphylococcus epidermidis, respectively, that act to synthesize a poly-beta-1,6-N-acetyl-d-glucosamine ECM required for biofilm formation. As with extracellular polysaccharide production in many other bacteria, synthesis of the Hms-dependent ECM is controlled by intracellular levels of cyclic-di-GMP. Yersinia pseudotuberculosis, the food- and water-borne enteric pathogen from which Y. pestis evolved recently, possesses identical hms genes and can form biofilm in vitro but not in the flea. The genetic changes in Y. pestis that resulted in adapting biofilm-forming capability to the flea gut environment, a critical step in the evolution of vector-borne transmission, have yet to be identified. During a flea bite, Y. pestis is regurgitated into the dermis in a unique biofilm phenotype, and this has implications for the initial interaction with the mammalian innate immune response.

Indexed as

AnimalsBiofilmsDisease Transmission, InfectiousHumansInsect VectorsPlagueSiphonapteraYersinia pestis

Identifiers

PMID18453279
PMCPMC3727414
OpenAlexW1604349669

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.