Evidence map›Paper›PMID 22844481›Full record

ArticlePloS one2012

Innate immune dysfunctions in aged mice facilitate the systemic dissemination of methicillin-resistant S. aureus.

Ching Wen Tseng, Pierre A Kyme, Andrea Arruda, V Krishnan Ramanujan, Wafa Tawackoli, George Y Liu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
2.6field-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

64 citing papers in PubMed, 109 citations in OpenAlex.

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  12. Regulatory RNAs in immunosenescence.Immunity, inflammation and disease · 2024
    Review
  13. Article
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  15. Review
  16. Review
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  18. Cellular Senescence in Immunity against Infections.International journal of molecular sciences · 2022
    Review
  19. Aging hampers neutrophil extracellular traps (NETs) efficacy.Aging clinical and experimental research · 2022
    Article
  20. Functional genomics of inflamm-aging and immunosenescence.Briefings in functional genomics · 2022
    Review

4 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

6 authors at 2 institutions in 1 country.

Ching Wen TsengDivision of Pediatric Infectious Diseases, Cedars-Sinai Medical Center, Los Angeles, California, United States of America. tsengcw@cshs.org
Pierre A Kyme
Andrea Arruda
V Krishnan Ramanujan
Wafa Tawackoli
George Y Liu
Cedars-Sinai Medical Center · USUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elderly humans show increased susceptibility to invasive staphylococcal disease after skin and soft tissue infection. However, it is not understood how host immunity changes with aging, and how that predisposes to invasive disease. In a model of severe skin infection, we showed that aged mice (16- to 20-month-old) exhibit dramatic bacterial dissemination compared with young adult mice (2-month-old). Bacterial dissemination was associated with significant reductions of CXCL1 (KC), polymorphonuclear cells (PMNs), and extracellular DNA traps (NETs) at the infection site. PMNs and primary skin fibroblasts isolated from aged mice showed decreased secretion of CXCL2 (MIP-2) and KC in response to MRSA, and in vitro analyses of mitochondrial functions revealed that the mitochondrial electron transport chain complex I plays a significant role in induction of chemokines in the cells isolated from young but not old mice. Additionally, PMNs isolated from aged mice have reduced ability to form NETs and to kill MRSA. Expression of nuclease by S. aureus led to increased bacterial systemic dissemination in young but not old mice, suggesting that defective NETs formation in elderly mice permitted nuclease and non-nuclease expressing S. aureus to disseminate equally well. Overall, these findings suggest that gross impairment of both skin barrier function and innate immunity contributes to the propensity for MRSA to disseminate in aged mice. Furthermore, the study indicates that contribution of bacterial factors to pathogenicity may vary with host age.

Indexed as

Immunity, InnateAgingAnimalsChemokinesDeoxyribonucleasesElectron Transport Complex IExtracellular SpaceFemaleMaleMethicillin-Resistant Staphylococcus aureusMiceNeutrophilsVirulence FactorsChemokinesDeoxyribonucleasesElectron Transport Complex IVirulence Factors

Identifiers

PMID22844481
PMCPMC3406035
OpenAlexW2019107501

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.