Rapid detection of methicillin resistance in coagulase-negative staphylococci with the VITEK 2 system

被引:14
作者
Horstkotte, MA [1 ]
Knobloch, JKM [1 ]
Rohde, H [1 ]
Dobinsky, S [1 ]
Mack, D [1 ]
机构
[1] Univ Hamburg, Klinikum Eppendorf, Inst Med Mikrobiol & Immunol, D-20246 Hamburg, Germany
关键词
D O I
10.1128/JCM.40.9.3291-3295.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The aim of the present study was to evaluate the accuracy of the new VITEK 2 system (bioMerieux, Marcy 1' Etoile, France) for the detection of methicillin resistance in coagulase-negative staphylococci (CoNS) by using AST-P515 and AST-P523 test cards. Analyses of the VITEK 2 oxacillin MIC determination evaluated according to the actual breakpoint ( greater than or equal to0.5 mug/ml) of the National Committee for Clinical Laboratory Standards resulted in a high sensitivity of 99.2% but a moderate specificity of 80%. The newly included oxacillin resistance (OR) test of the VITEK 2 system displayed a high sensitivity and a high specificity of 97.5 and 98.7%, respectively. Concordance between the results of the mecA PCR and the VITEK 2 oxacillin MIC was observed for almost all Staphylococcus epidermidis strains, but the reduced specificity was attributable to higher oxacillin MICs for mecA-negative non-S. epidermidis strains, especially S. saprophyticus, S. lugdunensis, and S. cohnii. Evaluation of alternative oxacillin MIC breakpoints of 1, 2, or 4 mug/ml resulted in improved degrees of specificity of 84, 90.7, and 97.3%, respectively. Only minor changes occurred in the corresponding sensitivity values, which were 98.4, 97.5, and 97.5%, respectively. Methicillin resistance in CoNS was detected after 7 and 8 h in 91.1 and 93.5% of the mecA-positive strains, respectively, by the VITEK 2 OR test and in 86.3 and 89.5% of the mecA-positive strains, respectively, by VITEK 2 oxacillin MIC determination. After 7 and 8 h the VITEK 2 OR test classified 59.2 and 78.9% of the mecA-negative strains, respectively, as susceptible to oxacillin, whereas comparable values were obtained 2 h later by VITEK 2 oxacillin MIC determination. The results of our study encourage the use of the VITEK 2 system, which proved to be a highly reliable and rapid phenotypic method for the detection of methicillin resistance in CoNS.
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页码:3291 / 3295
页数:5
相关论文
共 47 条
[1]   Establishing MIC breakpoints for coagulase-negative staphylococci to oxacillin [J].
Andrews, JM ;
Boswell, FJ ;
Wise, R .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 45 (02) :259-261
[2]  
[Anonymous], STAPHYLOCOCCI HUMAN
[3]   ANTIMICROBIAL SUSCEPTIBILITY OF COAGULASE-NEGATIVE STAPHYLOCOCCI [J].
ARCHER, GL ;
CLIMO, MW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (10) :2231-2237
[4]   Clinical and financial benefits of rapid bacterial identification and antimicrobial susceptibility testing [J].
Barenfanger, J ;
Drake, C ;
Kacich, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (05) :1415-1418
[5]   Validation of the VITEK2 and the Advance Expert System with a collection of Enterobacteriaceae harboring extended spectrum or inhibitor resistant β-lactamases [J].
Cantón, R ;
Pérez-Vázquez, M ;
Oliver, A ;
Coque, TM ;
Loza, E ;
Ponz, F ;
Baquero, F .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2001, 41 (1-2) :65-70
[6]   Methicillin resistance in staphylococci: Molecular and biochemical basis and clinical implications [J].
Chambers, HF .
CLINICAL MICROBIOLOGY REVIEWS, 1997, 10 (04) :781-+
[7]   CLINICAL IMPACT OF RAPID IN-VITRO SUSCEPTIBILITY TESTING AND BACTERIAL IDENTIFICATION [J].
DOERN, GV ;
VAUTOUR, R ;
GAUDET, M ;
LEVY, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (07) :1757-1762
[8]   Evaluation of the VITEK 2 system for rapid identification of medically relevant gram-negative rods [J].
Funke, G ;
Monnet, D ;
deBernardis, C ;
von Graevenitz, A ;
Freney, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (07) :1948-1952
[9]  
Garcia-Garrote F, 2000, J CLIN MICROBIOL, V38, P2108
[10]   National Nosocomial Infections Surveillance (NNIS) System report, data summary from January 1992-April 2000, issued June 2000 [J].
Gerberding, J ;
Gaynes, R ;
Horan, T ;
Alonso-Echanove, J ;
Edwards, J ;
Emori, G ;
Fridkin, S ;
Hageman, J ;
Henderson, T ;
Lawton, R ;
Peavy, G ;
Richards, C ;
Tolson, J ;
Wages, J .
AMERICAN JOURNAL OF INFECTION CONTROL, 2000, 28 (06) :429-448