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耐阿贝卡星、耐甲氧西林金黄色葡萄球菌引起的医院感染调查

Investigation of nosocomial infection caused by arbekacin-resistant, methicillin-resistant Staphylococcus aureus.

作者信息

Obayashi Y, Fujita J, Ichiyama S, Hojo S, Negayama K, Takashima C, Miyawaki H, Tanabe T, Yamaji Y, Kawanishi K, Takahara J

机构信息

First Department of Internal Medicine, Kagawa Medical University, Japan.

出版信息

Diagn Microbiol Infect Dis. 1997 Jun;28(2):53-9. doi: 10.1016/s0732-8893(97)00005-9.

Abstract

An outbreak of coagulase VII-producing, arbekacin (ABK)-resistant, methicillin-resistant Staphylococcus aureus (MRSA) occurred between September 1994 and December 1995, involving five different wards. Twenty-one patients developed skin, wound, drainage, or respiratory tract colonization with coagulase VII-producing, (ABK)-resistant MRSA. Phenotypic characteristics (production of enterotoxin and TSST-1, antimicrobial susceptibility) and molecular-typing procedure (plasmid DNA profile, pulsed-field gel electrophoresis [PFGE] and arbitrarily primed polymerase chain reaction [AP-PCR] of chromosomal DNA) in isolated strains were compared. Plasmid analysis identified four different profiles and 19 of 22 strains recovered had identical patterns. PFGE of chromosomal DNA identified three different subtypes and 18 (81.8%) isolates shared the same subtype. AP-PCR also demonstrated that most strains had the same phenotypic characteristics. Although traditional epidemiological methods; for example, coagulase typing, plays a central role in hospital infection control, combination of plasmid DNA profile, AP-PCR, and PFGE may prove to be a particularly informative means of tracking the nosocomial spread of MRSA.

摘要

1994年9月至1995年12月期间,发生了一起产凝固酶VII、耐阿贝卡星(ABK)、耐甲氧西林金黄色葡萄球菌(MRSA)的暴发,涉及五个不同病房。21名患者出现了产凝固酶VII、耐ABK的MRSA皮肤、伤口、引流物或呼吸道定植。对分离菌株的表型特征(肠毒素和TSST-1的产生、抗菌药敏性)和分子分型程序(质粒DNA图谱、脉冲场凝胶电泳[PFGE]以及染色体DNA的任意引物聚合酶链反应[AP-PCR])进行了比较。质粒分析确定了四种不同的图谱,回收的22株菌株中有19株具有相同模式。染色体DNA的PFGE确定了三种不同的亚型,18株(81.8%)分离株具有相同的亚型。AP-PCR也表明大多数菌株具有相同的表型特征。尽管传统的流行病学方法,例如凝固酶分型,在医院感染控制中起着核心作用,但质粒DNA图谱、AP-PCR和PFGE的联合应用可能被证明是追踪MRSA医院内传播的一种特别有效的手段。

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