Evidence map›Paper›PMID 24840573›Full record

ReviewInternational journal of molecular sciences2014

Colonization and infection of the skin by S. aureus: immune system evasion and the response to cationic antimicrobial peptides.

Sunhyo Ryu, Peter I Song, Chang Ho Seo, Hyeonsook Cheong, Yoonkyung Park

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% 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

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 131 citations in OpenAlex.

  1. Pooled it
  2. New microbes and new infections · 2026
    Review
  3. Monitoring the Burden ofAntibiotics (Basel, Switzerland) · 2026
    Article
  4. The Contribution of Human Antimicrobial Peptides to Fungi.International journal of molecular sciences · 2025
    Review
  5. Strategies for Survival ofInternational journal of molecular sciences · 2025
    Review
  6. Article
  7. DecipheringmSystems · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. The Plasmidomic Landscape of Clinical Methicillin-ResistantAntibiotics (Basel, Switzerland) · 2023
    Article
  14. Review
  15. Extracellular vesicles ofCurrent research in microbial sciences · 2023
    Article
  16. The Role ofInternational journal of molecular sciences · 2022
    Review
  17. Article
  18. Review
  19. A 3D-printed transepidermal microprojection array for human skin microbiome sampling.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  20. Article

2 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

5 authors at 3 institutions in 2 countries.

Sunhyo RyuDepartment of Biotechnology, Chosun University, Gwangju 501-759, Korea. bktsh0328@gmail.com.
Peter I SongDepartment of Dermatology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. psong@uams.edu.
Chang Ho SeoDepartment of Bioinformatics, Kongju National University, Kongju 314-701, Korea. chseo@kongju.ac.kr.
Hyeonsook CheongDepartment of Biotechnology, Chosun University, Gwangju 501-759, Korea. hscheong@chosun.ac.kr.
Yoonkyung ParkDepartment of Biotechnology, Chosun University, Gwangju 501-759, Korea. y_k_park@chosun.ac.kr.
Chosun University · KRKongju National University · KRUniversity of Arkansas for Medical Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staphylococcus aureus (S. aureus) is a widespread cutaneous pathogen responsible for the great majority of bacterial skin infections in humans. The incidence of skin infections by S. aureus reflects in part the competition between host cutaneous immune defenses and S. aureus virulence factors. As part of the innate immune system in the skin, cationic antimicrobial peptides (CAMPs) such as the β-defensins and cathelicidin contribute to host cutaneous defense, which prevents harmful microorganisms, like S. aureus, from crossing epithelial barriers. Conversely, S. aureus utilizes evasive mechanisms against host defenses to promote its colonization and infection of the skin. In this review, we focus on host-pathogen interactions during colonization and infection of the skin by S. aureus and methicillin-resistant Staphylococcus aureus (MRSA). We will discuss the peptides (defensins, cathelicidins, RNase7, dermcidin) and other mediators (toll-like receptor, IL-1 and IL-17) that comprise the host defense against S. aureus skin infection, as well as the various mechanisms by which S. aureus evades host defenses. It is anticipated that greater understanding of these mechanisms will enable development of more sustainable antimicrobial compounds and new therapeutic approaches to the treatment of S. aureus skin infection and colonization.

Indexed as

Anti-Infective AgentsAntimicrobial Cationic PeptidesHost-Pathogen InteractionsHumansImmune SystemInterleukinsMethicillin-Resistant Staphylococcus aureusSkinStaphylococcal InfectionsStaphylococcus aureusToll-Like ReceptorsAnti-Infective AgentsAntimicrobial Cationic PeptidesInterleukinsToll-Like Receptors

Identifiers

PMID24840573
PMCPMC4057757
OpenAlexW2013588152

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.