Evidence map›Paper›PMID 20979987›Full record

ArticleVaccine2010

Evaluation of Psn, HmuR and a modified LcrV protein delivered to mice by live attenuated Salmonella as a vaccine against bubonic and pneumonic Yersinia pestis challenge.

Christine G Branger, Wei Sun, Ascención Torres-Escobar, Robert Perry, Kenneth L Roland, Jacqueline Fetherston, Roy Curtiss

Abstract read
In one paragraph

Article in Vaccine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. RemodelingProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  2. Protective immunity enhancedFrontiers in immunology · 2022
    Article
  3. Review
  4. Biomolecules · 2020
    Review
  5. Article
  6. Article
  7. The Role of the Regulator Fur in Gene Regulation and Virulence ofFrontiers in cellular and infection microbiology · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Plague Vaccines: Status and Future.Advances in experimental medicine and biology · 2016
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Developing live vaccines against plague.Journal of infection in developing countries · 2011
    Review
  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

7 authors at 1 institution in 1 country.

Christine G BrangerCenter for Infectious Diseases and Vaccinology at Biodesign Institute and School of Life Sciences, PO Box 875401, Tempe, AZ 85287-5401, United States.
Wei Sun
Ascención Torres-Escobar
Robert Perry
Kenneth L Roland
Jacqueline Fetherston
Roy Curtiss
University of Kentucky · US

Funding

Attenuated Live and Recombinant Yersinia Pestis VaccinesR01AI057885 · NIAID · WASHINGTON UNIVERSITY · PI CURTISS III, ROY · 2004 to 2014
$4.8M
Salmonella Vaccines Against Bacterial EnteropathogensR01AI060557 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CURTISS III, ROY · 2010 to 2014
$2.2M
NIAID NIH HHS 5R01 AI057885NIAID NIH HHS R01 AI057885NIAID NIH HHS R01 AI060557
6 · The paper itself

Abstract

We evaluated the ability of Yersinia pestis antigens HmuR, Psn and modified forms of LcrV delivered by live attenuated Salmonella strains to stimulate a protective immune response against subcutaneous or intranasal challenge with Y. pestis CO92. LcrV196 is a previously described truncated protein that includes aa 131-326 of LcrV and LcrV5214 has been modified to replace five key amino acids required for interaction with the TLR2 receptor. Psn is the outer membrane receptor for the siderophore, yersiniabactin, and the bacteriocin, pesticin. Mice immunized with Salmonella synthesizing Psn, LcrV196 or LcrV5214 developed serum IgG responses to the respective Yersinia antigen and were protected against pneumonic challenge with Y. pestis. Immunization with Salmonella synthesizing Psn or LcrV196 was sufficient to afford nearly full protection against bubonic challenge, while immunization with the strain synthesizing LcrV5214 was not protective. Immunization with Salmonella synthesizing HmuR, an outer membrane protein involved in heme acquisition in Y. pestis, was poorly immunogenic and did not elicit a protective response against either challenge route. These findings indicate that both Psn and LcrV196 delivered by Salmonella provide protection against both bubonic and pneumonic plague.

Indexed as

AnimalsAntibodies, BacterialAntigens, BacterialBacterial ProteinsDisease Models, AnimalFemaleGenetic VectorsMiceMice, Inbred BALB CPlaguePlague VaccinePore Forming Cytotoxic ProteinsSalmonella VaccinesSurvival AnalysisVaccines, AttenuatedYersinia pestisAntibodies, BacterialAntigens, BacterialBacterial ProteinsLcrV protein, YersiniaPlague VaccinePore Forming Cytotoxic ProteinsSalmonella VaccinesVaccines, Attenuated

Identifiers

PMID20979987
PMCPMC3014047
OpenAlexW2059106032

What OpenQuestion holds

Textmetadata
LicenceTDM
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.