Hussain Zafar, Stoakes Luba, John Michael A, Garrow Shaunalee, Fitzgerald Viivi
Department of Microbiology and Infection Control, London Health Sciences Centre, University of Western Ontario, London, Ontario, Canada.
J Clin Microbiol. 2002 Jun;40(6):2251-3. doi: 10.1128/JCM.40.6.2251-2253.2002.
The methicillin resistance of 363 coagulase-negative staphylococci isolated from blood cultures was determined by a slide latex agglutination (LA) test for penicillin-binding protein 2a (PBP 2a), the presence of the mecA gene by PCR, disk diffusion, and Vitek. LA was performed on primary cultures, and PBP 2a expression was induced by placing an oxacillin disk in the primary inoculum. Compared to the PCR results, LA was the most sensitive and specific in the detection of methicillin resistance. Without induction, LA failed to detect 50% of mecA-positive strains grown on two different media.
采用针对青霉素结合蛋白2a(PBP 2a)的玻片乳胶凝集(LA)试验、聚合酶链反应(PCR)检测mecA基因、纸片扩散法及Vitek法,对从血培养中分离出的363株凝固酶阴性葡萄球菌的耐甲氧西林情况进行了测定。LA试验在原代培养物上进行,通过在原代接种物中放置苯唑西林纸片来诱导PBP 2a表达。与PCR结果相比,LA在检测耐甲氧西林方面最为敏感和特异。未经诱导时,LA未能检测出在两种不同培养基上生长的50%的mecA阳性菌株。