Methods for improved detection of oxacillin resistance in coagulase-negative staphylococci: Results of a multicenter study

被引:69
作者
Tenover, FC
Jones, RN
Swenson, JM
Zimmer, B
McAllister, S
Jorgensen, JH
机构
[1] Ctr Dis Control & Prevent, Hosp Infect Program, Nosocomial Pathogens Lab Branch G08, Atlanta, GA 30333 USA
[2] Univ Iowa, Coll Med, Dept Pathol, Iowa City, IA 52240 USA
[3] Dade MicroScan, W Sacramento, CA 95616 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Pathol, San Antonio, TX 78284 USA
关键词
D O I
10.1128/JCM.37.12.4051-4058.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 mu g of oxacillin per mi 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 greater than or equal to 4 to greater than or equal to 0.5 mu g/ml and the breakpoint for susceptibility should be lowered from less than or equal to 2 to less than or equal to 0.25 mu g/ml. In addition, a single disk diffusion breakpoint of less than or equal to 17 mm for resistance and greater than or equal to 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.
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页码:4051 / 4058
页数:8
相关论文
共 23 条
[1]   DETECTION OF METHICILLIN RESISTANCE IN STAPHYLOCOCCI BY USING A DNA PROBE [J].
ARCHER, GL ;
PENNELL, E .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (09) :1720-1724
[2]   Analysis of 281,797 consecutive blood cultures performed over an eight-year period: Trends in microorganisms isolated and the value of anaerobic culture of blood [J].
Cockerill, FR ;
Hughes, JG ;
Vetter, EA ;
Mueller, RA ;
Weaver, AL ;
Ilstrup, DM ;
Rosenblatt, JE ;
Wilson, WR .
CLINICAL INFECTIOUS DISEASES, 1997, 24 (03) :403-418
[3]   Phenotypic detection of mec A-positive staphylococcal blood stream isolates: High accuracy of simple disk diffusion tests [J].
Cormican, MG ;
Wilke, WW ;
Barrett, MS ;
Pfaller, MA ;
Jones, RN .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1996, 25 (03) :107-112
[4]  
DELANCASTER H, 1993, EUR J CLIN MICROBIOL, V12, P13
[5]  
Favero MS, 1996, AM J INFECT CONTROL, V24, P380
[6]   EFFECT OF SOURCE OF MUELLER-HINTON AGAR ON DETECTION OF OXACILLIN RESISTANCE IN STAPHYLOCOCCUS-AUREUS USING A SCREENING METHODOLOGY [J].
HINDLER, JA ;
WARNER, NL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (04) :734-735
[7]   2-PERCENT SODIUM-CHLORIDE IS REQUIRED FOR SUSCEPTIBILITY TESTING OF STAPHYLOCOCCI WITH OXACILLIN WHEN USING AGAR-BASED DILUTION METHODS [J].
HUANG, MB ;
GAY, TE ;
BAKER, CN ;
BANERJEE, SN ;
TENOVER, FC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (10) :2683-2688
[8]  
Kloos Wesley E., 1995, P282
[9]   EVIDENCE THAT THE NATIONAL-COMMITTEE-FOR-CLINICAL-LABORATORY-STANDARDS DISK TEST IS LESS SENSITIVE THAN THE SCREEN PLATE FOR DETECTION OF LOW-EXPRESSION-CLASS METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS [J].
MACKENZIE, AMR ;
RICHARDSON, H ;
LANNIGAN, R ;
WOOD, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (07) :1909-1911
[10]   Staphylococcus aureus and coagulase-negative staphylococci from blood stream infections:: Frequency of occurrence, antimicrobial susceptibility, and molecular (mecA) characterization of oxacillin resistance in the SCOPE program [J].
Marshall, SA ;
Wilke, WW ;
Pfaller, MA ;
Jones, RN .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1998, 30 (03) :205-214