Evidence map›Paper›PMID 23592990›Full record

ArticlePLoS pathogens2013

Mobile genetic element SCCmec-encoded psm-mec RNA suppresses translation of agrA and attenuates MRSA virulence.

Chikara Kaito, Yuki Saito, Mariko Ikuo, Yosuke Omae, Han Mao, Gentaro Nagano, Tomoko Fujiyuki, Shunsuke Numata, Xiao Han, Kazuaki Obata and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2013. 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
9.0field-weighted citation impact, top 1% 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, 116 citations in OpenAlex.

  1. Whole-genome sequencing ofMicrobiology spectrum · 2026
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  3. The Pathogenicity Mechanisms ofInternational journal of molecular sciences · 2025
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  8. The fitness connection of antibiotic resistance.Frontiers in microbiology · 2025
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  9. OralPathogens (Basel, Switzerland) · 2024
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  11. Methicillin Resistance Elements in the Canine PathogenAntibiotics (Basel, Switzerland) · 2024
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  12. Molecular Characteristics and Pathogenicity ofInternational journal of molecular sciences · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. The effect ofFrontiers in immunology · 2023
    Review
  17. Article
  18. Genotypes ofToxins · 2022
    Article
  19. Thirty Years of sRNA-Mediated Regulation inInternational journal of molecular sciences · 2022
    Review
  20. Article

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

16 authors at 5 institutions in 1 country.

Chikara KaitoGraduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan. kaito@mol.f.u-tokyo.ac.jp
Yuki Saito
Mariko Ikuo
Yosuke Omae
Han Mao
Gentaro Nagano
Tomoko Fujiyuki
Shunsuke Numata
Xiao Han
Kazuaki Obata
Setsuo Hasegawa
Hiroki Yamaguchi
Koiti Inokuchi
Teruyo Ito
Keiichi Hiramatsu
Kazuhisa Sekimizu
The University of Tokyo · JPJuntendo University · JPNippon Medical School · JPMinamiaoyama Eye Clinic · JPSeiwa Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Community acquired-methicillin resistant Staphylococcus aureus (CA-MRSA) is a socially problematic pathogen that infects healthy individuals, causing severe disease. CA-MRSA is more virulent than hospital associated-MRSA (HA-MRSA). The underlying mechanism for the high virulence of CA-MRSA is not known. The transcription product of the psm-mec gene, located in the mobile genetic element SCCmec of HA-MRSA, but not CA-MRSA, suppresses the expression of phenol-soluble modulin α (PSMα), a cytolytic toxin of S. aureus. Here we report that psm-mec RNA inhibits translation of the agrA gene encoding a positive transcription factor for the PSMα gene via specific binding to agrA mRNA. Furthermore, 25% of 325 clinical MRSA isolates had a mutation in the psm-mec promoter that attenuated transcription, and 9% of the strains had no psm-mec. In most of these psm-mec-mutated or psm-mec-deleted HA-MRSAs, PSMα expression was increased compared with strains carrying intact psm-mec, and some mutated strains produced high amounts of PSMα comparable with that of CA-MRSA. Deletion of psm-mec from HA-MRSA strains carrying intact psm-mec increased the expression of AgrA protein and PSMα, and virulence in mice. Thus, psm-mec RNA suppresses MRSA virulence via inhibition of agrA translation and the absence of psm-mec function in CA-MRSA causes its high virulence property.

Indexed as

Interspersed Repetitive SequencesAnimalsBacterial ToxinsCommunity-Acquired InfectionsFemaleMethicillin-Resistant Staphylococcus aureusMiceMutationPromoter Regions, GeneticProtein BindingRNA, BacterialRNA, MessengerStaphylococcal Skin InfectionsTranscription FactorsTranscription, GeneticBacterial ToxinsRNA, BacterialRNA, Messengerstaphylococcal delta toxinTranscription Factors

Identifiers

PMID23592990
PMCPMC3617227
OpenAlexW2159818846

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Registered trials

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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.