Evidence map›Paper›PMID 24957836›Full record

ArticleAntimicrobial agents and chemotherapy2014

Exposure of Staphylococcus aureus to subinhibitory concentrations of β-lactam antibiotics induces heterogeneous vancomycin-intermediate Staphylococcus aureus.

Mélanie Roch, Perrine Clair, Adriana Renzoni, Marie-Elisabeth Reverdy, Olivier Dauwalder, Michèle Bes, Annie Martra, Anne-Marie Freydière, Frédéric Laurent, Philippe Reix and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Linezolid MIC creep among clinically significantFrontiers in antibiotics · 2026
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  3. Characterisation ofJAC-antimicrobial resistance · 2025
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  5. Vancomycin heteroresistance among methicillin-resistant clinical isolates S. haemolyticus, S. hominis, S. simulans, and S. warneri.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2023
    Article
  6. Article
  7. Adaptive laboratory evolution and independent component analysis disentangle complex vancomycin adaptation trajectories.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Antibiotic Resistance and the MRSA Problem.Microbiology spectrum · 2019
    Review
  16. Article
  17. Characteristics ofBioMed research international · 2018
    Article
  18. Vancomycin Resistance inThe Yale journal of biology and medicine · 2017
    Review
  19. Article
  20. Review
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

12 authors at 3 institutions in 2 countries.

Mélanie RochInternational Center for Infectiology Research, Université de Lyon, Lyon, France INSERM U1111, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1, Lyon, France CNRS, UMR5308, Lyon, France Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France.
Perrine ClairHospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France.
Adriana RenzoniService of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.
Marie-Elisabeth ReverdyHospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France.
Olivier DauwalderInternational Center for Infectiology Research, Université de Lyon, Lyon, France INSERM U1111, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1, Lyon, France CNRS, UMR5308, Lyon, France Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France.
Michèle BesInternational Center for Infectiology Research, Université de Lyon, Lyon, France INSERM U1111, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1, Lyon, France CNRS, UMR5308, Lyon, France Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France.
Annie MartraHospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France.
Anne-Marie FreydièreHospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France.
Frédéric LaurentInternational Center for Infectiology Research, Université de Lyon, Lyon, France INSERM U1111, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1, Lyon, France CNRS, UMR5308, Lyon, France Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France.
Philippe ReixHospices Civils de Lyon, Centre de Référence Mucoviscidose, Lyon, France.
Oana DumitrescuInternational Center for Infectiology Research, Université de Lyon, Lyon, France INSERM U1111, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1, Lyon, France CNRS, UMR5308, Lyon, France Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France.
François VandeneschInternational Center for Infectiology Research, Université de Lyon, Lyon, France INSERM U1111, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1, Lyon, France CNRS, UMR5308, Lyon, France Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Lyon, France francois.vandenesch@univ-lyon1.fr.
Université Claude Bernard Lyon 1 · FRHospices Civils de Lyon · FRUniversity Hospital of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycopeptides are known to select for heterogeneous vancomycin-intermediate Staphylococcus aureus (h-VISA) from susceptible strains. In certain clinical situations, h-VISA strains have been isolated from patients without previous exposure to glycopeptides, such as cystic fibrosis patients, who frequently receive repeated treatments with beta-lactam antibiotics. Our objective was to determine whether prolonged exposure to beta-lactam antibiotics can induce h-VISA. We exposed 3 clinical vancomycin-susceptible methicillin-resistant Staphylococcus aureus (MRSA) strains to ceftazidime, ceftriaxone, imipenem, and vancomycin (as a control) at subinhibitory concentrations for 18 days in vitro. Population analyses showed progressive increases in vancomycin resistance; seven of the 12 derived strains obtained after induction were classified as h-VISA according to the following criteria: area under the curve (AUC) on day 18/AUC of Mu3 of ≥90% and/or growth on brain heart infusion (BHI) agar with 4 mg/liter vancomycin. The derived isolates had thickened cell walls proportional to the level of glycopeptide resistance. Genes known to be associated with glycopeptide resistance (vraSR, yvqF, SA1703, graRS, walKR, and rpoB) were PCR sequenced; no de novo mutations were observed upon beta-lactam exposure. To determine whether trfA, a gene encoding a glycopeptide resistance factor, was essential in the selection of h-VISA upon beta-lactam pressure, a trfA-knockout strain was generated by allelic replacement. Indeed, beta-lactam exposure of this mutated strain showed no capacity to induce vancomycin resistance. In conclusion, these results showed that beta-lactam antibiotics at subinhibitory concentrations can induce intermediate vancomycin resistance in vitro. This induction required an intact trfA locus. Our results suggest that prior use of beta-lactam antibiotics can compromise vancomycin efficacy in the treatment of MRSA infections.

Indexed as

Anti-Bacterial Agentsbeta-LactamsCeftazidimeCeftriaxoneDrug Resistance, BacterialImipenemMethicillin ResistanceMicrobial Sensitivity TestsMicroscopy, Electron, TransmissionStaphylococcus aureusVancomycinVancomycin ResistanceAnti-Bacterial Agentsbeta-LactamsCeftazidimeCeftriaxoneImipenemVancomycin

Identifiers

PMID24957836
PMCPMC4135816
OpenAlexW2146405701

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.