Institut für Medizinische Mikrobiologie, Universität Zürich, Zürich, Schweiz.
Clin Microbiol Infect. 2012 Dec;18(12):1194-204. doi: 10.1111/j.1469-0691.2011.03737.x. Epub 2012 Jan 20.
This study aimed to develop a modular, diagnostic algorithm for extended spectrum β-lactamase (ESBL) detection in Enterobacteriaceae. Clinical Enterobacteriaceae strains (n = 2518) were screened for ESBL production using Clinical and Laboratory Standards Institute (CLSI) breakpoints for third-generation cephalosporins and by synergy image detection (clavulanic acid/extended-spectrum cephalosporins). Isolates screening positive for ESBL (n = 242, 108 by critical CLSI diameters alone, five by double disk synergy test (DDST) alone, and 129 by both critical diameters and DDST) and 138 ESBL screening negative isolates (control group) were investigated by molecular methods considered to be the reference standard (multiplex CTX-M type PCR, TEM and SHV type sequence characterization). One hundred and twenty-four out of 242 Enterobacteriaceae isolates screening positive for ESBL were confirmed to be ESBL positive by the reference standard, the majority of them in E. coli, K. pneumoniae and E. cloacae (94, 17 and nine isolates, respectively). Prevalence of ESBL production ranged from <1% for P. mirabilis to 4.7%, 5.1% and 6.6%, for K. pneumoniae, E. cloacae and E. coli, respectively. Combining CLSI ceftriaxone and cefpodoxime critical ESBL diameters was found to be the most sensitive phenotypic screening method (sensitivity 99.2%). Combining critical diameters of cefpodoxime and ceftriaxone with DDST for cefpodoxime resulted in a sensitivity of 100%. For phenotypic confirmation, combining the CLSI recommended combined disk test (CDT) for ceftazidime and cefotaxime amended with a cefepime CDT was highly sensitive (100%) and specific (97.5%). With respect to the studied population, the diagnostic ESBL algorithm developed would have resulted in sensitivity and specificity of 100%. The corresponding flow chart is simple, easy to use, inexpensive and applicable in the routine diagnostic laboratory.
本研究旨在开发一种用于检测肠杆菌科中扩展谱β-内酰胺酶(ESBL)的模块化诊断算法。使用临床和实验室标准协会(CLSI)针对第三代头孢菌素的折点和协同图像检测(克拉维酸/扩展谱头孢菌素)对临床肠杆菌科菌株(n=2518)进行 ESBL 产生的筛选。对 ESBL 筛选阳性的分离株(n=242,242 株中 108 株仅根据关键 CLSI 直径阳性,5 株仅根据双碟协同试验(DDST)阳性,129 株根据关键直径和 DDST 均阳性)和 138 株 ESBL 筛选阴性的分离株(对照组)进行了分子方法研究,这些方法被认为是参考标准(多重 CTX-M 型 PCR、TEM 和 SHV 型序列特征)。242 株 ESBL 筛选阳性的肠杆菌科分离株中,有 124 株经参考标准确认为 ESBL 阳性,其中大多数为大肠埃希菌、肺炎克雷伯菌和阴沟肠杆菌(94、17 和 9 株)。ESBL 产生的流行率从奇异变形杆菌的<1%到肺炎克雷伯菌、阴沟肠杆菌和大肠埃希菌的分别为 4.7%、5.1%和 6.6%。将 CLSI 头孢曲松和头孢泊肟的临界 ESBL 直径结合起来,发现这是最敏感的表型筛选方法(灵敏度 99.2%)。将头孢泊肟和头孢曲松的临界直径与头孢泊肟的 DDST 结合起来,可使灵敏度达到 100%。对于表型确认,将 CLSI 推荐的头孢他啶和头孢噻肟联合药敏纸片试验(CDT)与头孢吡肟 CDT 结合起来,具有很高的灵敏度(100%)和特异性(97.5%)。对于研究人群,开发的诊断 ESBL 算法将具有 100%的敏感性和特异性。相应的流程图简单、易用、价格低廉,适用于常规诊断实验室。