A PCR assay for rapid detection of vancomycin-resistant enterococci

被引:28
作者
Pérez-Hernández, X
Méndez-Alvarez, S
Claverie-Martín, F [1 ]
机构
[1] Candelaria Univ Hosp, Nuestra Senora, Res Unit, Mol Biol Lab, Santa Cruz de Tenerife, Spain
[2] Univ La Laguna, Dept Cellular Biol & Microbiol, Santa Cruz de Tenerife, Spain
关键词
D O I
10.1016/S0732-8893(01)00360-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Since the first report of a vancomycin-resistant enterococcal clinical isolate, these Gram-positive bacteria have emerged as important nosocomial pathogens. Several glycopeptide resistance phenotypes can be distinguished on the basis of the level and inducibility of resistance to vancomycin and teicoplanin. In the present study, we developed a multiplex PCR, which allows the simultaneous identification of enterococci at the genus level and detection of the most frequent glycopeptide resistance genotypes. Five primer sets targeting the genes vanA, vanB, vanC1, vanC2/C3 and tuf were used in one reaction tube with bacterial DNA extracted from three to five colonies. This PCR method is Suitable for the rapid detection of vancomycin-resistant enterococci. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:273 / 277
页数:5
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