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Article Abstract

(1) Background: Linezolid plays an important role in the treatment of invasive infections caused by vancomycin-resistant enterococci after its introduction to clinical practice. However, a detailed examination of linezolid-nonsusceptible enterococci (LNSE) is required. In this study, we attempted to analyze the mechanisms of LNSE strains isolated from a tertiary care hospital. (2) Methods: From 2019 to 2020, 18 , 14 and 2 clinical isolates were collected at Severance Hospital. Agar dilution was performed to evaluate precise linezolid minimum inhibitory concentrations (MICs). Short-read whole-genome sequencing (WGS) was used to analyze resistance determinants. (3) Results: The presence of the gene was likely the primary resistance mechanism in these three species, typically demonstrating a MIC value of 8 μg/mL. The co-existence of the and gene was the second major mechanism, primarily predicting a phenotype showing intermediate susceptibility to linezolid. G2576U mutation on 23S rRNA was only found in ; it mediated the most significant increase in linezolid MIC. (4) Conclusion: This is the first report examining co-harboring clinical enterococcal isolates in Korea and demonstrating the -harboring clinical strain worldwide. The comparison with resistance-gene-containing fragments in the isolates obtained from different countries and different sources demonstrated the spread of linezolid-resistance genes and suggested the possibility of foodborne transmission.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686573PMC
http://dx.doi.org/10.3390/antibiotics11111624DOI Listing

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Article Synopsis
  • Linezolid is crucial for treating invasive infections from vancomycin-resistant enterococci, but more research on linezolid-nonsusceptible enterococci (LNSE) is needed as seen in this study.
  • The study analyzed 34 clinical strains from Severance Hospital between 2019 and 2020, assessing linezolid resistance through agar dilution and whole-genome sequencing to identify the mechanisms.
  • Key findings revealed that specific genes were the primary resistance mechanisms, with one mutation leading to significantly increased linezolid resistance, highlighting concerns about the spread of these resistance genes and potential foodborne transmission.
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Purpose: To investigate linezolid-resistance mechanisms in linezolid-nonsusceptible enterococci (LNSE) isolated from a tertiary hospital in Korea.

Methodology: Enterococcal isolates exhibiting linezolid MICs ≥4 mg l that were isolated between December 2011 and May 2016 were investigated by PCR and sequencing for mutations in 23S rRNA or ribosomal proteins (L3, L4 and L22) and for the presence of cfr, cfr(B) and optrA genes.Results/Key findings.

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This report describes linezolid susceptibility testing results for 6,741 Gram-positive pathogens from 60 U.S. sites collected during 2015 for the LEADER Program.

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Investigation of Linezolid Resistance in Staphylococci and Enterococci.

J Clin Microbiol

May 2016

Department of Pathology and Immunology, Department of Pediatrics, and Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA

Article Synopsis
  • - The study aimed to explore an increase in linezolid-nonsusceptible staphylococci and enterococci after switching to an automated antimicrobial susceptibility testing system.
  • - Testing 27 nonsusceptible isolates revealed that only 70 to 75% confirmed resistance through various methods, indicating poor agreement between testing techniques.
  • - Genetic analysis found mutations linked to linezolid resistance in 59.3% of isolates and identified new variants that could also play a role in resistance.
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Thelinezolidexperience andaccuratedetermination ofresistance (LEADER) surveillance program has monitored linezolid activity, spectrum, and resistance since 2004. In 2014, a total of 6,865 Gram-positive pathogens from 60 medical centers from 36 states were submitted. The organism groups evaluated wereStaphylococcus aureus(3,106), coagulase-negative staphylococci (CoNS; 797), enterococci (855),Streptococcus pneumoniae(874), viridans group streptococci (359), and beta-hemolytic streptococci (874).

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