Linezolid resistance: detection of the cfr(B) gene in French clinical MRSA strains.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
01 02 2023
Historique:
received: 31 08 2022
accepted: 15 11 2022
pubmed: 13 12 2022
medline: 3 2 2023
entrez: 12 12 2022
Statut: ppublish

Résumé

To describe two linezolid-resistant MRSA strains carrying the cfr(B) gene detected in the French National Reference Centre for staphylococci. Two linezolid-resistant MRSA strains isolated from cystic fibrosis patients in two different French hospitals in 2017 and 2019 were examined to explore the mechanisms of linezolid resistance. Antimicrobial susceptibility was tested using broth microdilution and gradient strips. The genetic determinants of linezolid resistance were assessed by a multiplex PCR targeting cfr/cfr(B), optrA and poxtA genes, by amplification and sequencing of individual 23S rRNA genes and by WGS using both Illumina and Nanopore technologies. The two MRSA strains were resistant to linezolid but susceptible to tedizolid, and PCR-positive for cfr/cfr(B). The WGS analysis indicated that they belonged to two different STs (ST8-MRSA-IV and ST5382-MRSA-IV) and that they both harboured the cfr(B) gene on the same 9.7 kb Tn6218-like chromosomal transposon, a finding only previously reported in Enterococcus sp. and Clostridioides difficile. To the best of our knowledge, this is the first description of the presence of cfr(B) in staphylococci, more specifically in linezolid-resistant MRSA strains. This finding illustrates the risk of horizontal intergenus transfer of oxazolidinone resistance genes in Staphylococcus aureus and highlights the need to monitor such emergence in this species.

Identifiants

pubmed: 36509546
pii: 6889549
doi: 10.1093/jac/dkac411
doi:

Substances chimiques

Linezolid ISQ9I6J12J
Anti-Bacterial Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

445-449

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Benjamin Youenou (B)

Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Institut des Agents Infectieux, Lyon F-69004, France.

Patricia Martins Simoes (P)

Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Institut des Agents Infectieux, Lyon F-69004, France.
Equipe Pathogénie des staphylocoques, CIRI, Centre International de Recherche en Infectiologie, Université de Lyon, Inserm U1111, Université Claude Bernard Lyon 1, CNRS UMR5308, ENS de Lyon, France.

Anne Tristan (A)

Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Institut des Agents Infectieux, Lyon F-69004, France.
Equipe Pathogénie des staphylocoques, CIRI, Centre International de Recherche en Infectiologie, Université de Lyon, Inserm U1111, Université Claude Bernard Lyon 1, CNRS UMR5308, ENS de Lyon, France.

Eric Farfour (E)

Hôpital Foch, Service de Biologie clinique, Suresnes F-92150, France.

Clémence Beauruelle (C)

University Brest, INSERM, EFS, UMR 1078, GGB, Brest F-29200, France.
Department of Bacteriology, Virology, Brest University Hospital, Hospital Hygiene, and Parasitology-Mycology, Brest F-29200, France.

Camille Kolenda (C)

Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Institut des Agents Infectieux, Lyon F-69004, France.
Equipe Pathogénie des staphylocoques, CIRI, Centre International de Recherche en Infectiologie, Université de Lyon, Inserm U1111, Université Claude Bernard Lyon 1, CNRS UMR5308, ENS de Lyon, France.

Anne-Gaëlle Ranc (AG)

Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Institut des Agents Infectieux, Lyon F-69004, France.
Equipe Pathogénie des staphylocoques, CIRI, Centre International de Recherche en Infectiologie, Université de Lyon, Inserm U1111, Université Claude Bernard Lyon 1, CNRS UMR5308, ENS de Lyon, France.

François Vandenesch (F)

Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Institut des Agents Infectieux, Lyon F-69004, France.
Equipe Pathogénie des staphylocoques, CIRI, Centre International de Recherche en Infectiologie, Université de Lyon, Inserm U1111, Université Claude Bernard Lyon 1, CNRS UMR5308, ENS de Lyon, France.

Frédéric Laurent (F)

Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Institut des Agents Infectieux, Lyon F-69004, France.
Equipe Pathogénie des staphylocoques, CIRI, Centre International de Recherche en Infectiologie, Université de Lyon, Inserm U1111, Université Claude Bernard Lyon 1, CNRS UMR5308, ENS de Lyon, France.

Céline Dupieux (C)

Hospices Civils de Lyon, Centre National de Référence des Staphylocoques, Institut des Agents Infectieux, Lyon F-69004, France.
Equipe Pathogénie des staphylocoques, CIRI, Centre International de Recherche en Infectiologie, Université de Lyon, Inserm U1111, Université Claude Bernard Lyon 1, CNRS UMR5308, ENS de Lyon, France.

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