The reliability of Microscan™ conventional and rapid panels to identify Staphylococcus aureus and detect methicillin resistance:: An evaluation using the tube coagulase test and mecA PCR

被引:7
作者
Farrell, DJ [1 ]
机构
[1] Queensland Hlth Pathol Serv, Toowoomba Lab, Dept Pathol, Microbiol Sect, Toowoomba, Qld 4350, Australia
关键词
Staphylococcus aureus; mecA; Microscan; Etest; PCR; methicillin resistance;
D O I
10.1080/00313029700169405
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Microscan(TM) (Dade Diagnostics, Brisbane) Positive Combo Type 6 (312 panels) and Rapid Positive Breakpoint Type 1 (62 panels) were evaluated for Staphylococcus aureus identification, using the tube coagulase test (TC), and oxacillin susceptibility, using mecA. A total of 374 consecutive clinical staphylococci were tested, with TC and Microscan(TM) having 100% correlation (335 identified as S. aureus and 39 as coagulase negative staphylococci by both methods). A 93% correlation was observed between Microscan(TM) and mecA PCR for oxacillin susceptibility. No very major errors (0/374 false oxacillin susceptibility) and 26 (7%) major errors (26/374 false oxacillin resistance) were found showing false resistance to oxacillin to be a problem in our population. Oxacillin Etest (AB Biodisk, Sweden) was performed on all oxacillin resistant isolates. A bimodal distribution was observed between mecA positive and negative isolates. A testing algorithm (using the Microscan(TM) panels and Etest) was developed for this laboratory to detect mecA encoded methicillin resistance. Retrospective application of this algorithm to the 374 isolates gave 100% correlation with mecA detection.
引用
收藏
页码:406 / 410
页数:5
相关论文
共 26 条
[21]   NEW MECHANISM FOR METHICILLIN RESISTANCE IN STAPHYLOCOCCUS-AUREUS - CLINICAL ISOLATES THAT LACK THE PBP-2A GENE AND CONTAIN NORMAL PENICILLIN-BINDING PROTEINS WITH MODIFIED PENICILLIN-BINDING CAPACITY [J].
TOMASZ, A ;
DRUGEON, HB ;
DELENCASTRE, HM ;
JABES, D ;
MCDOUGALL, L ;
BILLE, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (11) :1869-1874
[22]   COMPARISON OF TESTS FOR DETECTION OF METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS IN A CLINICAL MICROBIOLOGY LABORATORY [J].
UNAL, S ;
WERNER, K ;
DEGIROLAMI, P ;
BARSANTI, F ;
ELIOPOULOS, G .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (02) :345-347
[23]   DETECTION OF METHICILLIN-RESISTANT STAPHYLOCOCCI BY USING THE POLYMERASE CHAIN-REACTION [J].
UNAL, S ;
HOSKINS, J ;
FLOKOWITSCH, JE ;
WU, CYE ;
PRESTON, DA ;
SKATRUD, PL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (07) :1685-1691
[24]   COMPARISON OF THE AUTOSCAN-W/A AND VITEK AUTOMICROBIC SYSTEMS FOR IDENTIFICATION AND SUSCEPTIBILITY TESTING OF BACTERIA [J].
VISSER, MR ;
BOGAARDS, L ;
ROZENBERGARSKA, M ;
VERHOEF, J .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1992, 11 (11) :979-984
[25]   SOUTHERN HYBRIDIZATION ANALYSIS OF THE MECA DELETION FROM METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS [J].
WADA, A ;
KATAYAMA, Y ;
HIRAMATSU, K ;
YOKOTA, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 176 (03) :1319-1325
[26]   LABORATORY DIAGNOSIS OF OXACILLIN RESISTANCE IN STAPHYLOCOCCUS-AUREUS BY A MULTIPLEX-POLYMERASE CHAIN-REACTION ASSAY [J].
ZAMBARDI, G ;
REVERDY, ME ;
BLAND, S ;
BES, M ;
FRENEY, J ;
FLEURETTE, J .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1994, 19 (01) :25-31