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Journal of Antimicrobial Chemotherapy (2003) 51, 186-188
© 2003 The British Society for Antimicrobial Chemotherapy


Correspondence

Linezolid resistance in clinical isolates of Staphylococcus aureus

Peter Wilson1,*, J. A. Andrews1, R. Charlesworth1, R. Walesby2, M. Singer3, D. J. Farrell4 and M. Robbins4

1 University College London Hospital, Department of Clinical Microbiology, London; 2 University College London Hospital, Cardiothoracic Surgery, London; 3 Royal Free and University College London Medical School, Bloomsbury Institute of Intensive Care, London; 4 GR Micro Ltd, London, UK

Keywords: oxazolidinone, resistance, Staphylococcus aureus, linezolid

The first 10% of the full text of this article appears below.

Sir,

Linezolid is the first oxazolidinone antibiotic to be licensed for treatment of Gram-positive infections. It is active against methicillin-resistant Staphylococcus aureus (MRSA), glycopeptide-intermediate S. aureus (GISA) and vancomycin-resistant enterococci (VRE).1 It inhibits the formation of the initiation complex formed with mRNA, fMet-tRNA and the 30S ribosomal subunit. Mutations to the central loop of domain V of 23S rRNA have been associated with resistance to linezolid in several species in vitro.2 There has been one report of resistance of MRSA in a clinical infection, a patient with dialysis-related peritonitis.3 . . . [Full Text of this Article]

Acknowledgements


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