Kobayashi M, Ohara-Nemoto Y, Kaneko M
Department of Microbiology, School of Dentistry, Iwate Medical University, Morioka, Japan.
Kansenshogaku Zasshi. 1997 Jul;71(7):620-7. doi: 10.11150/kansenshogakuzasshi1970.71.620.
Genotyping of 67 clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA) separated from patients in a hospital in Mizusawa City in 1994 and 1995 was studied by pulsed field gel electrophoresis (PFGE) and arbitrarily primed-polymerase chain reaction (AP-PCR). Two main genotypes were observed by PFGE, and more than 70% of the 67 MRSA isolates produced coagulase type II. One group diverged well and gained higher tolerance in 1994, but was not isolated in 1995. The other group was continually isolated during the two-year period and showed moderate tolerance in 1994, and higher tolerance in 1995. AP-PCR was able to classify the genotypes of MRSA into 6 subgenotypes under the present conditions, which supported the results obtained by PFGE. These results suggest that AP-PCR could become a convenient and useful typing method by improving both sequence and length of a primer.
1994年和1995年从水泽市一家医院的患者身上分离出67株耐甲氧西林金黄色葡萄球菌(MRSA)临床分离株,采用脉冲场凝胶电泳(PFGE)和任意引物聚合酶链反应(AP-PCR)对其进行基因分型研究。通过PFGE观察到两种主要基因型,67株MRSA分离株中70%以上产生II型凝固酶。一组在1994年分化良好且耐受性增强,但在1995年未分离到。另一组在这两年期间持续分离,1994年显示中等耐受性,1995年耐受性增强。在当前条件下,AP-PCR能够将MRSA基因型分为6个亚型,这支持了PFGE获得的结果。这些结果表明,通过改进引物的序列和长度,AP-PCR可能成为一种方便且有用的分型方法。