Evidence map›Paper›PMID 20160020›Full record

ArticleInfection and immunity2010

The yersiniabactin transport system is critical for the pathogenesis of bubonic and pneumonic plague.

Jacqueline D Fetherston, Olga Kirillina, Alexander G Bobrov, James T Paulley, Robert D Perry

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

75 citing papers in PubMed, 118 citations in OpenAlex.

  1. Article
  2. Environmental and Host Blood Interactions ShapePathogens (Basel, Switzerland) · 2026
    Article
  3. Journal of fungi (Basel, Switzerland) · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Non-classical roles of bacterial siderophores in pathogenesis.Frontiers in cellular and infection microbiology · 2024
    Review
  10. Article
  11. Article
  12. Genomic Analysis ofPathogens (Basel, Switzerland) · 2023
    Article
  13. Overview ofBiology · 2023
    Review
  14. A frameshift ineLife · 2023
    Article
  15. Zoonoses (Shannon, Ireland) · 2023
    Article
  16. Article
  17. Review
  18. Attenuation ofFrontiers in cellular and infection microbiology · 2022
    Article
  19. Article
  20. Yersiniabactin contributes to overcoming zinc restriction duringProceedings of the National Academy of Sciences of the United States of America · 2021
    Article

15 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

5 authors at 1 institution in 1 country.

Jacqueline D FetherstonDepartment of Microbiology, Immunology, and Molecular Genetics, MS415 Medical Center, University of Kentucky, Lexington, KY 40536-0298, USA.
Olga Kirillina
Alexander G Bobrov
James T Paulley
Robert D Perry
University of Kentucky · US

Funding

Yersiniabactin and plague pathogenesisR01AI033481 · NIAID · UNIVERSITY OF KENTUCKY · PI PERRY, ROBERT DONALD · 1993 to 2013
$3.6M
Yersiniabactin and plague pathogenesisR56AI033481 · NIAID · UNIVERSITY OF KENTUCKY · PI PERRY, ROBERT DONALD · 2008 to 2008
$366k
NIAID NIH HHS AI-33481NIAID NIH HHS R01 AI033481NIAID NIH HHS R56 AI033481
6 · The paper itself

Abstract

Iron acquisition from the host is an important step in the pathogenic process. While Yersinia pestis has multiple iron transporters, the yersiniabactin (Ybt) siderophore-dependent system plays a major role in iron acquisition in vitro and in vivo. In this study, we determined that the Ybt system is required for the use of iron bound by transferrin and lactoferrin and examined the importance of the Ybt system for virulence in mouse models of bubonic and pneumonic plague. Y. pestis mutants unable to either transport Ybt or synthesize the siderophore were both essentially avirulent via subcutaneous injection (bubonic plague model). Surprisingly, via intranasal instillation (pneumonic plague model), we saw a difference in the virulence of Ybt biosynthetic and transport mutants. Ybt biosynthetic mutants displayed an approximately 24-fold-higher 50% lethal dose (LD(50)) than transport mutants. In contrast, under iron-restricted conditions in vitro, a Ybt transport mutant had a more severe growth defect than the Ybt biosynthetic mutant. Finally, a Delta pgm mutant had a greater loss of virulence than the Ybt biosynthetic mutant, indicating that the 102-kb pgm locus encodes a virulence factor, in addition to Ybt, that plays a role in the pathogenesis of pneumonic plague.

Indexed as

AnimalsFemaleIronLethal Dose 50MicePhenolsPlagueSurvival AnalysisThiazolesVirulenceVirulence FactorsYersinia pestisIronPhenolsThiazolesVirulence Factorsyersiniabactin

Identifiers

PMID20160020
PMCPMC2863531
OpenAlexW2136182602

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.