Persistence and evolution of linezolid- and methicillin-resistant Staphylococcus epidermidis ST2 and ST5 clones in an Italian hospital.

ST2 ST5 Staphylococcus epidermidis cfr linezolid resistance plasmid ribosomal mutations rpoB

Journal

Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459

Informations de publication

Date de publication:
06 Feb 2024
Historique:
received: 09 08 2023
revised: 18 01 2024
accepted: 30 01 2024
medline: 9 2 2024
pubmed: 9 2 2024
entrez: 8 2 2024
Statut: aheadofprint

Résumé

Staphylococcus epidermidis is a member of the human skin microbiome. However, in recent decades multidrug-resistant and hospital-adapted S. epidermidis clones are increasingly involved in severe human infections associated to medical devices and in immunocompromisedpatients. In 2016, we reported that a linezolid- and methicillin-resistant S. epidermidis ST2 clone, bearing the G2576T mutation, was endemic in an Italian hospital since 2004. To retrospectively analyze 34 linezolid- and methicillin-resistant S. epidermidis (LR-MRSE) strains collected from 2018 to 2021 from the same hospital. LR-MRSE were typed by PFGE and MLST and screened for transferable linezolid resistance genes. Representative LR-MRSE were subjected to WGS and their resistomes, including the presence of ribosomal mechanisms of linezolid resistance and of rpoB gene mutations conferring rifampin resistance, were investigated. ST2 lineage was still prevalent (19/34; 55.9%), but, over time, ST5 clone has been widespread too (15/34; 44.1%). Thirteen of the 34 isolates (38.2%) were positive for the cfr gene. WGS analysis of relevant LR-MRSE displayed complex resistomes for the presence of several acquired antibiotic resistance genes including the SCCmec type III (3A) and SCCmec type IV (2B) in ST2 and ST5 isolates, respectively. Bioinformatics and PCR mapping also showed a plasmid-location of the cfr gene and the occurrence of previously undetected mutations in L3 (ST2 lineage) and L4 (ST3 lineage) ribosomal proteins and substitutions in rpoB gene. The occurrence of LR-MRSE should be carefully monitored in order to prevent the spread of this difficult-to-treat pathogen and to preserve the efficacy of linezolid.

Sections du résumé

BACKGROUND BACKGROUND
Staphylococcus epidermidis is a member of the human skin microbiome. However, in recent decades multidrug-resistant and hospital-adapted S. epidermidis clones are increasingly involved in severe human infections associated to medical devices and in immunocompromisedpatients. In 2016, we reported that a linezolid- and methicillin-resistant S. epidermidis ST2 clone, bearing the G2576T mutation, was endemic in an Italian hospital since 2004.
AIM OBJECTIVE
To retrospectively analyze 34 linezolid- and methicillin-resistant S. epidermidis (LR-MRSE) strains collected from 2018 to 2021 from the same hospital.
METHODS METHODS
LR-MRSE were typed by PFGE and MLST and screened for transferable linezolid resistance genes. Representative LR-MRSE were subjected to WGS and their resistomes, including the presence of ribosomal mechanisms of linezolid resistance and of rpoB gene mutations conferring rifampin resistance, were investigated.
RESULTS RESULTS
ST2 lineage was still prevalent (19/34; 55.9%), but, over time, ST5 clone has been widespread too (15/34; 44.1%). Thirteen of the 34 isolates (38.2%) were positive for the cfr gene. WGS analysis of relevant LR-MRSE displayed complex resistomes for the presence of several acquired antibiotic resistance genes including the SCCmec type III (3A) and SCCmec type IV (2B) in ST2 and ST5 isolates, respectively. Bioinformatics and PCR mapping also showed a plasmid-location of the cfr gene and the occurrence of previously undetected mutations in L3 (ST2 lineage) and L4 (ST3 lineage) ribosomal proteins and substitutions in rpoB gene.
CONCLUSIONS CONCLUSIONS
The occurrence of LR-MRSE should be carefully monitored in order to prevent the spread of this difficult-to-treat pathogen and to preserve the efficacy of linezolid.

Identifiants

pubmed: 38331029
pii: S2213-7165(24)00026-2
doi: 10.1016/j.jgar.2024.01.020
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Auteurs

Marzia Cinthi (M)

Department of Life and Environmental Sciences, Polytechnic University of Marche, Ancona, Italy.

Sonia Nina Coccitto (SN)

Department of Biomedical Sciences and Public Health, Polytechnic University of Marche, Ancona, Italy.

Antonella Pocognoli (A)

Clinical Microbiology Laboratory, Azienda Ospedaliero-Universitaria, Ospedali Riuniti, Ancona, Italy.

Guido Zeni (G)

Department of Diagnostics and Public Health, Verona University, Verona, Italy.

Annarita Mazzariol (A)

Department of Diagnostics and Public Health, Verona University, Verona, Italy.

Alessandra Di Gregorio (AD)

Department of Life and Environmental Sciences, Polytechnic University of Marche, Ancona, Italy.

Carla Vignaroli (C)

Department of Life and Environmental Sciences, Polytechnic University of Marche, Ancona, Italy.

Brenciani Andrea (B)

Department of Biomedical Sciences and Public Health, Polytechnic University of Marche, Ancona, Italy. Electronic address: a.brenciani@univpm.it.

Eleonora Giovanetti (E)

Department of Life and Environmental Sciences, Polytechnic University of Marche, Ancona, Italy.

Classifications MeSH