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[使用乳胶凝集试剂盒检测青霉素结合蛋白2对耐甲氧西林金黄色葡萄球菌进行鉴定的评估]

[Evaluation of MRSA identification with latex agglutination kit for the detection of penicillin-binding protein 2].

作者信息

Ito Y, Morita E, Moriyama M, Kuono H, Tanaka K, Kato N, Watanabe K

机构信息

Internal Medicine, Japan.

出版信息

Rinsho Biseibutshu Jinsoku Shindan Kenkyukai Shi. 2001;12(1):9-13.

Abstract

MRSA is one of the major nosocomial pathogens, and methicillin-resistance is associated with acquisition of the mecA gene coding for the penicillin-binding protein 2' (PBP2'). MRSA-screen test (Denka Seiken Co., Ltd., Tokyo, Japan) is a slide latex agglutination kit which can detect PBP2' within 15 min. MRSA-screen test was compared with PCR for detection of the mecA gene in order to detect MRSA. S. aureus strains isolated from April to October in 1999 in Gifu Red Cross Hospital were identified as 25 MRSA and 19 MSSA by susceptibility testing to oxacillin by the agar dilution method according to the recommendation of the National Comittee for the Clinical Laboratory Standards. The MRSA screen test and PCR for the mecA gene showed sensitivites of 92.0 and 96.0% and specificities of 89.5 and 94.7%, respectively. It is considered that MRSA-screen is a rapid and reliable test for discrimination of MRSA from MSSA colonies on agar plates.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)是主要的医院病原体之一,耐甲氧西林与编码青霉素结合蛋白2'(PBP2')的mecA基因的获得有关。MRSA筛查试验(日本东京Denka Seiken有限公司)是一种玻片乳胶凝集试剂盒,可在15分钟内检测出PBP2'。为了检测MRSA,将MRSA筛查试验与检测mecA基因的聚合酶链反应(PCR)进行了比较。根据美国国家临床实验室标准委员会的建议,采用琼脂稀释法对岐阜红十字医院1999年4月至10月分离的金黄色葡萄球菌菌株进行苯唑西林敏感性试验,鉴定出25株MRSA和19株甲氧西林敏感金黄色葡萄球菌(MSSA)。MRSA筛查试验和检测mecA基因的PCR的敏感性分别为92.0%和96.0%,特异性分别为89.5%和94.7%。认为MRSA筛查是一种从琼脂平板上的MSSA菌落中鉴别MRSA的快速可靠的试验。

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