Evidence map›Paper›PMID 19164505›Full record

ArticleThe American journal of pathology2009

Pneumonic plague pathogenesis and immunity in Brown Norway rats.

Deborah M Anderson, Nancy A Ciletti, Hanni Lee-Lewis, Derek Elli, Joshua Segal, Kristin L DeBord, Katie A Overheim, Maria Tretiakova, Robert R Brubaker, Olaf Schneewind

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Antimicrobial Treatment and Prophylaxis of Plague: Recommendations for Naturally Acquired Infections and Bioterrorism Response.MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports · 2021
    Guideline
  2. Microscopic and Molecular Identification ofAnimals : an open access journal from MDPI · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Protecting against plague: towards a next-generation vaccine.Clinical and experimental immunology · 2013
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Plague: Infections of Companion Animals and Opportunities for Intervention.Animals : an open access journal from MDPI · 2011
    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

10 authors at 3 institutions in 1 country.

Deborah M AndersonDepartment of Veterinary Pathobiology, University of Missouri, 302 Connaway Hall, 1600 E. Rollins St., Columbia, MO 65211, USA. andersondeb@missouri.edu
Nancy A Ciletti
Hanni Lee-Lewis
Derek Elli
Joshua Segal
Kristin L DeBord
Katie A Overheim
Maria Tretiakova
Robert R Brubaker
Olaf Schneewind
University of Chicago · USMissouri College · USUniversity of Missouri · US

Funding

LcrV Plague Vaccine with Altered Immune Modulatory PropertiesU01AI070559 · NIAID · UNIVERSITY OF CHICAGO · PI SCHNEEWIND, OLAF · 2006 to 2008
$6.5M
POSTDOCTORAL TRAINING IN LABORATORY ANIMAL MEDICINET32RR007004 · NCRR · UNIVERSITY OF MISSOURI-COLUMBIA · PI BRYDA, ELIZABETH C, FRANKLIN, CRAIG L · 1985 to 2011
$3.3M
AZOLE-RESISTANT CANDIDA IN MARROW TRANSPLANT PATIENTSK08AI001571 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MARR, KIEREN A. · 1999 to 2003
$481k
NCRR NIH HHS T32 RR007004NIAID NIH HHS U01 AI070559NIAID NIH HHS U54 AI0157153
6 · The paper itself

Abstract

The Brown Norway rat was recently described as a bubonic plague model that closely mimics human disease. We therefore evaluated the Brown Norway rat as an alternative small animal model for pneumonic plague and characterized both the efficacy and potency of vaccine candidates. When infected by intranasal instillation, these rats rapidly developed fatal pneumonic plague within 2 to 4 days of infection. Plague disease was characterized by severe alveolar edema and vascular hemorrhage in the lung in addition to fulminant necrotizing pneumonia caused by massive bacterial replication and inflammation. Twenty-four hours before death, animals developed systemic disease with an apparent delayed inflammatory response. We evaluated the ability of the protective antigen, LcrV, and a mutant derivative, V10, to protect these rats from pneumonic plague. Both were highly effective vaccines because complete protection was observed at challenge doses of 7500 LD(50). Antibody analyses suggested stronger potency of V10 immune sera compared with LcrV in the passive transfer of immunity to bubonic plague, with multiple neutralizing epitopes in LcrV. Taken together, these data demonstrate the effectiveness of inhibiting type III secretion in the prevention of pneumonic plague in rats and reveal critical contributions from both the cellular and humoral immune systems. Thus, the Brown Norway rat is an appealing alternative small animal model for the study of pneumonic plague pathogenesis and immunity.

Indexed as

AnimalsBacterial VaccinesDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFemaleHumansImmunization, PassiveInflammationIntradermal TestsLethal Dose 50PlagueRatsRats, Inbred BNYersinia pestisBacterial Vaccines

Identifiers

PMID19164505
PMCPMC2665751
OpenAlexW2019956770

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.