Crnich Christopher J, Duster Megan, Warrack Simone, Maki Dennis, Safdar Nasia
University of Wisconsin, School of Medicine and Public Health, Madison, Wisconsin, USA William S. Middleton Veterans Affairs Hospital, Madison, Wisconsin, USA
University of Wisconsin, School of Medicine and Public Health, Madison, Wisconsin, USA.
J Clin Microbiol. 2014 Jun;52(6):2027-32. doi: 10.1128/JCM.03466-13. Epub 2014 Mar 26.
Pulsed-field gel electrophoresis (PFGE) is a common method used to type methicillin-resistant Staphylococcus aureus (MRSA) in nosocomial investigations and epidemiological studies but is time-consuming and methodologically challenging. We compared typing results obtained using a commercial repetitive-element PCR (rep-PCR) system with PFGE in a sample of 86 unique MRSA isolates recovered from subjects in an academic referral hospital and two nursing homes in the same geographic region. Both methods reliably assigned isolates to the same Centers for Disease Control and Prevention (CDC) pulsotype. PFGE was significantly more discriminatory (Simpson's index of diversity, 0.92 at the 95% strain similarity threshold) than the commercial rep-PCR system (Simpson's index of diversity, 0.58). The global (adjusted Rand coefficient, 0.10) and directional congruence (adjusted Wallace coefficient(repPCR→PFGE) = 0.06; adjusted Wallace coefficient(PFGE → repPCR) = 0.52) between the two methods was low. MRSA strains recovered from study nursing homes that were clonal when typed by the commercial rep-PCR method were frequently noted to be genetically distinct when typed using PFGE. These data suggest that the commercial rep-PCR has less utility than PFGE in small-scale epidemiological assessments of MRSA in health care settings.
脉冲场凝胶电泳(PFGE)是医院感染调查和流行病学研究中用于对耐甲氧西林金黄色葡萄球菌(MRSA)进行分型的常用方法,但该方法耗时且在方法学上具有挑战性。我们在从同一地理区域的一家学术转诊医院和两家疗养院的受试者中分离出的86株独特MRSA菌株样本中,比较了使用商业重复元件PCR(rep-PCR)系统与PFGE获得的分型结果。两种方法都能可靠地将菌株归为相同的美国疾病控制与预防中心(CDC)脉冲型。PFGE的鉴别力明显高于商业rep-PCR系统(在95%菌株相似性阈值下,PFGE的辛普森多样性指数为0.92,商业rep-PCR系统的辛普森多样性指数为0.58)。两种方法之间的总体一致性(调整后的兰德系数,0.10)和方向性一致性(调整后的华莱士系数(repPCR→PFGE)=0.06;调整后的华莱士系数(PFGE→repPCR)=0.52)较低。通过商业rep-PCR方法分型为克隆型的研究疗养院中分离出的MRSA菌株,在使用PFGE分型时通常被发现具有不同的遗传特征。这些数据表明,在医疗保健环境中对MRSA进行小规模流行病学评估时,商业rep-PCR的实用性不如PFGE。