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Journal of Clinical Microbiology, December 1999, p. 4051-4058, Vol. 37, No. 12
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Methods for Improved Detection of Oxacillin
Resistance in Coagulase-Negative Staphylococci: Results of a
Multicenter Study
Fred C.
Tenover,1,*
Ronald N.
Jones,2
Jana M.
Swenson,1
Barbara
Zimmer,3
Sigrid
McAllister,1 and
James H.
Jorgensen4,
for the Nccls
Staphylococcus Working Group
Hospital Infections Program, Centers for Disease Control
and Prevention, Atlanta, Georgia 303331;
Department of Pathology, University of Iowa College of
Medicine, Iowa City, Iowa 522402; Dade
MicroScan, West Sacramento, California 956163;
and Department of Pathology, The University of Texas
Health Science Center, San Antonio, Texas 782844
Received 12 April 1999/Returned for modification 26 July
1999/Accepted 1 September 1999
A multilaboratory study was undertaken to determine the accuracy of
the current National Committee for Clinical Laboratory Standards
(NCCLS) oxacillin breakpoints for broth microdilution and disk
diffusion testing of coagulase-negative staphylococci (CoNS) by using a
PCR assay for mecA as the reference method. Fifty
well-characterized strains of CoNS were tested for oxacillin susceptibility by the NCCLS broth microdilution and disk diffusion procedures in 11 laboratories. In addition, organisms were inoculated onto a pair of commercially prepared oxacillin agar screen plates containing 6 µg of oxacillin per ml and 4% NaCl. The results of this
study and of several other published reports suggest that, in order to
reliably detect the presence of resistance mediated by
mecA, the oxacillin MIC breakpoint for defining resistance in CoNS should be lowered from
4 to
0.5 µg/ml and the breakpoint for susceptibility should be lowered from
2 to
0.25 µg/ml. In addition, a single disk diffusion breakpoint of
17 mm for resistance and
18 mm for susceptibility is suggested. Due to the poor
sensitivity of the oxacillin agar screen plate for predicting
resistance in this study, this test can no longer be recommended for
use with CoNS. The proposed interpretive criteria for testing CoNS have been adopted by the NCCLS.
*
Corresponding author. Mailing address: Nosocomial
Pathogens Laboratory Branch (G08), Hospital Infections Program, Centers for Disease Control and Prevention, 1600 Clifton Rd., Atlanta, GA
30333. Phone: (404) 639-3246. Fax: (404) 639-1381. E-mail: fnt1{at}CDC.GOV.

The other members of the NCCLS Staphylococcus Working Group are
William J. Buesching and Robert J. Fass, Ohio State University
Medical
Center, Columbus; James D. Dick, The Johns Hopkins Hospital,
Baltimore,
Md.; Patrick R. Murray, Barnes-Jewish Hospital, St.
Louis, Mo.;
Lance R. Peterson, Northwestern Memorial Hospital,
Chicago, Ill.;
L. Barth Reller, Duke University Medical Center,
Durham, N.C.;
Melvin P. Weinstein, UMDNJ-Robert Wood Johnson Medical
School, New
Brunswick, N.J.; and Mary K. York, University of California,
San
Francisco.
Journal of Clinical Microbiology, December 1999, p. 4051-4058, Vol. 37, No. 12
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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