Tokue Y, Shoji S, Satoh K, Watanabe A, Motomiya M
Department of Internal Medicine, Tohoku University, Miyagi, Japan.
Antimicrob Agents Chemother. 1992 Jan;36(1):6-9. doi: 10.1128/AAC.36.1.6.
The presence or absence of a methicillin resistance gene in 58 clinical isolates of Staphylococcus aureus was examined by the polymerase chain reaction (PCR) and Southern blot analyses. The results were analyzed in relation to those of the MIC assay of methicillin and oxacillin. PCR assay results were identical to those of Southern blot analysis of genomic DNA digested with HindIII (positive, 28 strains; negative, 30 strains). Among the 28 PCR-positive strains, 6 strains showed methicillin susceptibility by the conventional susceptibility test (MICs, less than or equal to 8 micrograms/ml). Culturing of the six strains with ceftizoxime led to an increase in the phenotypic level of resistance to methicillin and oxacillin, indicating that these strains should be classified as methicillin-resistant S. aureus (MRSA). The PCR assay was found to be a sensitive and reliable procedure for the rapid diagnosis of MRSA infection, even in cases in which the conventional MIC assay failed to detect MRSA.
采用聚合酶链反应(PCR)和Southern印迹分析检测了58株金黄色葡萄球菌临床分离株中耐甲氧西林基因的有无。并将结果与甲氧西林和苯唑西林的最低抑菌浓度(MIC)测定结果进行了分析。PCR检测结果与用HindIII消化的基因组DNA的Southern印迹分析结果一致(阳性28株;阴性30株)。在28株PCR阳性菌株中,6株通过传统药敏试验显示对甲氧西林敏感(MICs小于或等于8微克/毫升)。用头孢唑肟培养这6株菌株导致对甲氧西林和苯唑西林的表型耐药水平增加,表明这些菌株应归类为耐甲氧西林金黄色葡萄球菌(MRSA)。结果发现,即使在传统MIC测定未能检测到MRSA的情况下,PCR检测仍是快速诊断MRSA感染的灵敏可靠方法。