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Journal of Clinical Microbiology, February 2007, p. 329-332, Vol. 45, No. 2
0095-1137/07/$08.00+0     doi:10.1128/JCM.01508-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

A Multicenter Study Evaluating the Current Strategies for Isolating Staphylococcus aureus Strains with Reduced Susceptibility to Glycopeptides{triangledown}

Mandy Wootton,1* Alasdair P. MacGowan,2 Timothy R. Walsh,3 and Robin A. Howe1

Specialist Antimicrobial Chemotherapy Unit, NPHS Microbiology Cardiff, University Hospital Wales, Heath Park, Cardiff CF14 4XW, United Kingdom,1 Bristol Centre for Antimicrobial Research and Evaluation (BCARE), Medical Microbiology, Southmead Hospital, North Bristol Healthcare Trust, Bristol BS10 5NB, United Kingdom,2 Department of Medical Microbiology, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, United Kingdom3

Received 21 July 2006/ Returned for modification 5 October 2006/ Accepted 6 November 2006

Glycopeptide-intermediate Staphylococcus aureus (GISA) and heterogeneous GISA (hGISA) strains are notoriously difficult to detect in the diagnostic laboratory. The clinical importance of GISA, and particularly hGISA, will only be obvious when a definitive detection method is available. A few novel GISA and hGISA detection methods have been proposed; however, their validity has never been tested on a significant scale and in different laboratories. This study compares three screening methods for detecting GISA and hGISA strains in 12 laboratories, using a blind panel of 48 strains with known glycopeptide susceptibilities. The three screening methods used were brain heart infusion agar with 6 mg/liter vancomycin (BHIA6V) (CDC/CLSI), Mueller-Hinton agar with 5 mg/liter teicoplanin (MHA5T) (European Antimicrobial Resistance Surveillance System [EARSS]), and the macrodilution method Etest (MET) (EARSS), with population analysis profile-area under the curve analysis as the gold standard. Sensitivity and specificity were highest for MHA5T and MET, which identified 82.5% and 85.9% of strains, respectively. BHIA6V had poor sensitivity, particularly for hGISA (11.5% of strains were detected), and gave the largest interlaboratory variation in performance. MET exhibited the least interlaboratory variation. It is essential that laboratories use appropriate methods to detect GISA/hGISA strains so that the prevalence and clinical importance of these strains can be assessed properly.


* Corresponding author. Mailing address: BCARE, Department of Cellular and Molecular Medicine, Medical Sciences, University of Bristol, Bristol BS8 1TD, United Kingdom. Phone: 44 117 3317658. Fax: 44 117 9287896. E-mail: mandy.wootton{at}bristol.ac.uk.

{triangledown} Published ahead of print on 15 November 2006.


Journal of Clinical Microbiology, February 2007, p. 329-332, Vol. 45, No. 2
0095-1137/07/$08.00+0     doi:10.1128/JCM.01508-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




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