Evidence map›Paper›PMID 22869727›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Protection from the acquisition of Staphylococcus aureus nasal carriage by cross-reactive antibody to a pneumococcal dehydrogenase.

Rebeccah S Lijek, Santiago L Luque, Qian Liu, Dane Parker, Taeok Bae, Jeffrey N Weiser

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

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

  1. The association between bacteria colonizing the upper respiratory tract and lower respiratory tract infection in young children: a systematic review and meta-analysis.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2021
    Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
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  10. Article
  11. Article
  12. Observational
  13. Role of Proline in Pathogen and Host Interactions.Antioxidants & redox signaling · 2019
    Review
  14. Structural Biology of Proline Catabolic Enzymes.Antioxidants & redox signaling · 2019
    Review
  15. Article
  16. Review
  17. Review
  18. Humanized Mouse Models ofFrontiers in immunology · 2017
    Review
  19. Frontiers in veterinary science · 2017
    Article
  20. 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

6 authors at 4 institutions in 1 country.

Rebeccah S LijekDepartment of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Santiago L Luque
Qian Liu
Dane Parker
Taeok Bae
Jeffrey N Weiser
University of Pennsylvania · USColumbia University · USIndiana University Northwest · USIndiana University School of Medicine

Funding

Training in Emerging Infectious DiseasesT32AI055400 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI CHERRY, SARA, HENSLEY, SCOTT ERIC · 2003 to 2022
$4.4M
Prophage contribution to the virulence of Staphylococcus aureusR01AI077564 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI BAE, TAEOK · 2009 to 2013
$1.5M
NIAID NIH HHS AI-055400NIAID NIH HHS R01 AI077564NIAID NIH HHS T32 AI055400
6 · The paper itself

Abstract

Nasal colonization by Staphylococcus aureus is the major risk factor for disease and transmission. Epidemiological studies have reported a reduced risk of S. aureus carriage in immunocompetent but not in immunocompromised children colonized by Streptococcus pneumoniae. We investigate the hypothesis that the immune response to pneumococcal colonization affects S. aureus colonization. We demonstrate that pneumococcal colonization in mice inhibits subsequent S. aureus acquisition in an antibody-dependent manner and elicits antibody that cross-reacts with S. aureus. We identify the staphylococcal target of cross-reactive antibody as 1-pyrroline-5-carboxylate dehydrogenase (P5CDH), and the homologous immunogen in S. pneumoniae as SP_1119, both of which are conserved dehydrogenases. These antigens are necessary and sufficient to inhibit the acquisition of S. aureus colonization in a mouse model. Our findings demonstrate that immune-mediated cross-reactivity between S. pneumoniae and S. aureus protects against S. aureus nasal acquisition and thus reveal a paradigm for identifying protective antigens against S. aureus.

Indexed as

AnimalsAntigensCarrier StateGene DeletionMethicillin-Resistant Staphylococcus aureusMiceModels, GeneticMutationNasal MucosaOxidoreductasesPneumococcal VaccinesRecombinant ProteinsStaphylococcal InfectionsStaphylococcus aureusStreptococcus pneumoniaeAntigensOxidoreductasesPneumococcal VaccinesRecombinant Proteins

Identifiers

PMID22869727
PMCPMC3427079
OpenAlexW2153094083

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.