Evidence map›Paper›PMID 22869569›Full record

ArticleAntimicrobial agents and chemotherapy2012

DNA microarray profiling of a diverse collection of nosocomial methicillin-resistant staphylococcus aureus isolates assigns the majority to the correct sequence type and staphylococcal cassette chromosome mec (SCCmec) type and results in the subsequent identification and characterization of novel SCCmec-SCCM1 composite islands.

Anna C Shore, Orla M Brennan, Emily C Deasy, Angela S Rossney, Peter M Kinnevey, Ralf Ehricht, Stefan Monecke, David C Coleman

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

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

  1. Pooled it
  2. Trial
  3. Methicillin-ResistantAntibiotics (Basel, Switzerland) · 2025
    Article
  4. Molecular epidemiology of methicillin-resistantFrontiers in microbiology · 2025
    Review
  5. Article
  6. Characterizing a Novel Staphylococcal Cassette ChromosomeAntimicrobial agents and chemotherapy · 2021
    Article
  7. Epidemiological typing of methicillin resistantInfection prevention in practice · 2021
    Article
  8. Article
  9. Livestock-Associated Methicillin-ResistantFrontiers in microbiology · 2019
    Review
  10. Article
  11. Distribution of the Most PrevalentFrontiers in microbiology · 2018
    Review
  12. Characterization of the virulence potential ofNew microbes and new infections · 2017
    Article
  13. Evaluation of HiaureusJournal of clinical and diagnostic research : JCDR · 2017
    Article
  14. Review
  15. Characterization of Methicillin-ResistantFrontiers in microbiology · 2016
    Article
  16. Coagulase-negative staphylococci.Clinical microbiology reviews · 2014
    Review
  17. Article
  18. Article
  19. Article
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 3 institutions in 2 countries.

Anna C ShoreMicrobiology Research Unit, Dublin Dental University Hospital, University of Dublin, Trinity College, Dublin, Ireland.
Orla M Brennan
Emily C Deasy
Angela S Rossney
Peter M Kinnevey
Ralf Ehricht
Stefan Monecke
David C Coleman
Dublin Dental University Hospital · IEAlere (Germany) · DESt. James's Hospital · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One hundred seventy-five isolates representative of methicillin-resistant Staphylococcus aureus (MRSA) clones that predominated in Irish hospitals between 1971 and 2004 and that previously underwent multilocus sequence typing (MLST) and staphylococcal cassette chromosome mec (SCCmec) typing were characterized by spa typing (175 isolates) and DNA microarray profiling (107 isolates). The isolates belonged to 26 sequence type (ST)-SCCmec types and subtypes and 35 spa types. The array assigned all isolates to the correct MLST clonal complex (CC), and 94% (100/107) were assigned an ST, with 98% (98/100) correlating with MLST. The array assigned all isolates to the correct SCCmec type, but subtyping of only some SCCmec elements was possible. Additional SCCmec/SCC genes or DNA sequence variation not detected by SCCmec typing was detected by array profiling, including the SCC-fusidic acid resistance determinant Q6GD50/fusC. Novel SCCmec/SCC composite islands (CIs) were detected among CC8 isolates and comprised SCCmec IIA-IIE, IVE, IVF, or IVg and a ccrAB4-SCC element with 99% DNA sequence identity to SCC(M1) from ST8/t024-MRSA, SCCmec VIII, and SCC-CI in Staphylococcus epidermidis. The array showed that the majority of isolates harbored one or more superantigen (94%; 100/107) and immune evasion cluster (91%; 97/107) genes. Apart from fusidic acid and trimethoprim resistance, the correlation between isolate antimicrobial resistance phenotype and the presence of specific resistance genes was ≥97%. Array profiling allowed high-throughput, accurate assignment of MRSA to CCs/STs and SCCmec types and provided further evidence of the diversity of SCCmec/SCC. In most cases, array profiling can accurately predict the resistance phenotype of an isolate.

Indexed as

Bacterial ProteinsFusidic AcidMethicillin-Resistant Staphylococcus aureusMultilocus Sequence TypingOligonucleotide Array Sequence AnalysisTrimethoprimBacterial ProteinsFusidic AcidTrimethoprim

Identifiers

PMID22869569
PMCPMC3457404
OpenAlexW2140091216

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.