Evidence map›Paper›PMID 23289889›Full record

ArticleBMC microbiology2013

Molecular characterization of methicillin-resistant Panton-valentine leukocidin positive staphylococcus aureus clones disseminating in Tunisian hospitals and in the community.

Ben Jomàa-Jemili Mariem, Teruyo Ito, Meng Zhang, Jingxun Jin, Shanshuang Li, Boutiba-Ben Boubaker Ilhem, Hammami Adnan, Xiao Han, Keiichi Hiramatsu

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  4. Methicillin-ResistantAntibiotics (Basel, Switzerland) · 2023
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  6. Comparative Genomic Analysis of a Multidrug-ResistantPathogens (Basel, Switzerland) · 2022
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  7. Article
  8. Article
  9. Molecular Characterization ofPathogens (Basel, Switzerland) · 2021
    Article
  10. Article
  11. Article
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  13. Article
  14. Determining the Biofilm Forming Gene Profile ofReports of biochemistry & molecular biology · 2019
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

9 authors at 4 institutions in 2 countries.

Ben Jomàa-Jemili MariemDepartment of Infection Control Science, Juntendo University, Tokyo, Japan.
Teruyo Ito
Meng Zhang
Jingxun Jin
Shanshuang Li
Boutiba-Ben Boubaker Ilhem
Hammami Adnan
Xiao Han
Keiichi Hiramatsu
Juntendo University · JPHopital Universitaire Habib Bourguiba · TNTunis El Manar University · TNTunis University · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe spread of MRSA strains at hospitals as well as in the community are of great concern worldwide. We characterized the MRSA clones isolated at Tunisian hospitals and in the community by comparing them to those isolated in other countries.

resultsWe characterized 69 MRSA strains isolated from two Tunisian university hospitals between the years 2004-2008. Twenty-two of 28 (79%) community-associated MRSA (CA-MRSA) strains and 21 of 41 (51%) healthcare-associated MRSA (HA-MRSA) strains were PVL-positive. The PVL-positive strains belonged to predicted founder group (FG) 80 in MLST and carried either type IVc SCCmec or nontypeable SCCmec that harbours the class B mec gene complex. In contrast, very diverse clones were identified in PVL-negative strains: three FGs (5, 15, and 22) for HA-MRSA strains and four FGs (5, 15, 45, and 80) for CA-MRSA strains; and these strains carried the SCCmec element of either type I, III, IVc or was nontypeable. The nucleotide sequencing of phi7401PVL lysogenized in a CA-MRSA strain JCSC7401, revealed that the phage was highly homologous to phiSA2mw, with nucleotide identities of more than 95%. Furthermore, all PVL positive strains were found to carry the same PVL phage, since these strains were positive in two PCR studies, identifying gene linkage between lukS and mtp (major tail protein) and the lysogeny region, both of which are in common with phi7401PVL and phiSa2mw.

conclusionsOur experiments suggest that FG80 S. aureus strains have changed to be more virulent by acquiring phi7401PVL, and to be resistant to β-lactams by acquiring SCCmec elements. These novel clones might have disseminated in the Tunisian community as well as at the Tunisian hospitals by taking over existing MRSA clones.

Indexed as

Bacterial Toxinsbeta-Lactam ResistanceCommunity-Acquired InfectionsCross InfectionDNA, BacterialExotoxinsGenotypeHospitals, UniversityHumansLeukocidinsMethicillin-Resistant Staphylococcus aureusMolecular EpidemiologyMolecular Sequence DataMultilocus Sequence TypingProphagesSequence Homology, Nucleic AcidBacterial ToxinsDNA, BacterialExotoxinsLeukocidinsPanton-Valentine leukocidinVirulence Factors

Identifiers

PMID23289889
PMCPMC3544733
OpenAlexW2043514148

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LicenceCC BY
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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.