Evidence map›Paper›PMID 23008447›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

Failure to induce IFN-β production during Staphylococcus aureus infection contributes to pathogenicity.

Amber Kaplan, Jun Ma, Pierre Kyme, Andrea J Wolf, Courtney A Becker, Ching Wen Tseng, George Y Liu, David M Underhill

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

28 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Virulence · 2023
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. The Role of Macrophages inFrontiers in immunology · 2020
    Review
  13. Toll-like receptor 2-dependent endosomal signaling byThe Journal of biological chemistry · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Direct Antimicrobial Activity of IFN-β.Journal of immunology (Baltimore, Md. : 1950) · 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

8 authors at 1 institution in 1 country.

Amber KaplanInflammatory Bowel and Immunobiology Research Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Jun Ma
Pierre Kyme
Andrea J Wolf
Courtney A Becker
Ching Wen Tseng
George Y Liu
David M Underhill
Cedars-Sinai Medical Center · US

Funding

Phagosomal targeting of CARD proteinsR01GM085796 · NIGMS · CEDARS-SINAI MEDICAL CENTER · PI UNDERHILL, DAVID M. · 2008 to 2020
$4.1M
Antioxidant-based mechanisms used by staphyloccocus aureus to evade host defensesR01AI074832 · NIAID · CEDARS-SINAI MEDICAL CENTER · PI LIU, GEORGE Y · 2007 to 2010
$1.6M
The Cedars-Sinai Immunobiology Training ProgramT32AI089553 · NIAID · CEDARS-SINAI MEDICAL CENTER · PI ARDITI, MOSHE, TARGAN, STEPHAN R. · 2010 to 2016
$1.1M
NIAID NIH HHS R01 AI074832NIAID NIH HHS T32 AI089553NIAID NIH HHS T32 AI089553-01NIGMS NIH HHS R01 GM085796
6 · The paper itself

Abstract

The importance of type I IFNs in the host response to viral infection is well established; however, their role in bacterial infection is not fully understood. Several bacteria (both Gram-positive and -negative) have been shown to induce IFN-β production in myeloid cells, but this IFN-β is not always beneficial to the host. We examined whether Staphylococcus aureus induces IFN-β from myeloid phagocytes, and if so, whether it is helpful or harmful to the host to do so. We found that S. aureus poorly induces IFN-β production compared with other bacteria. S. aureus is highly resistant to degradation in the phagosome because it is resistant to lysozyme. Using a mutant that is more sensitive to lysozyme, we show that phagosomal degradation and release of intracellular ligands is essential for induction of IFN-β and inflammatory chemokines downstream of IFN-β. Further, we found that adding exogenous IFN-β during S. aureus infection (in vitro and in vivo) was protective. Together, the data demonstrate that failure to induce IFN-β production during S. aureus infection contributes to pathogenicity.

Indexed as

Interferon-betaAnimalsCells, CulturedDisease Models, AnimalHumansMiceMice, Inbred C57BLMice, KnockoutMutationStaphylococcal InfectionsStaphylococcus aureusInterferon-beta

Identifiers

PMID23008447
PMCPMC3478442
OpenAlexW2168617764

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.