Departamento de Microbiología, Facultad de Medicina, Universidad Autónoma de Nuevo León, Monterrey, Nuevo León, Mexico.
Hospital Universitario 'Dr José Eleuterio González', Universidad Autónoma de Nuevo León, Monterrey, Nuevo Leon, Mexico.
J Med Microbiol. 2011 Jan;60(Pt 1):84-90. doi: 10.1099/jmm.0.022970-0. Epub 2010 Oct 7.
Our objective was to analyse phenotypic and genetic data of extended-spectrum β-lactamase (ESBL)-producing Klebsiella pneumoniae, Enterobacter cloacae, Escherichia coli and Serratia marcescens that cause infections in our hospital. Over a 3 year period, 342 randomly selected clinical Enterobacteriaceae isolates were tested for ESBL production and evaluated for the presence of the β-lactamase genes bla(SHV), bla(TEM,) bla(CTX-M) and bla(TLA-1). The antibiotic susceptibilities of these isolates were also determined, and the clonality of the isolates was assessed by PFGE. Based on our analyses, 33/92 (35.9 %) K. pneumoniae, 31/87 (35.6 %) Enterobacter cloacae, 24/80 (30 %) E. coli and 17/83 (20.5 %) S. marcescens were identified as ESBL producers. The presence of TEM, SHV or CTX ESBL types was detected in 99/105 (94 %) of the isolates. TLA-1 was not detected in any of the 105 isolates. The dominant ESBL types were bla(SHV-5) (n=33), bla(SHV12) (n=31) and bla(CTX-M-15) (n=30). The predominant ESBL identified in E. coli and Enterobacter cloacae isolates was CTX-M-15, whereas in K. pneumoniae and S. marcescens the predominant types were SHV-12 and SHV-5, respectively. PFGE genotyping revealed two main genetic patterns in the K. pneumoniae isolates, types SHV-12 and TEM-1+SHV-5. An outbreak caused by Enterobacter cloacae SHV-5+CTX-M-15 was detected. In contrast, most ESBL-producing isolates of E. coli and S. marcescens did not have similar PFGE banding patterns and thus were not genetically similar. Enterobacteriaceae are a concern in our hospital, especially K. pneumoniae and Enterobacter cloacae. Our results confirm that the CTX-M-15 ESBL type has spread rapidly in the hospital, and thus requires careful monitoring.
我们的目的是分析引起我院感染的产超广谱β-内酰胺酶(ESBL)的肺炎克雷伯菌、阴沟肠杆菌、大肠埃希菌和黏质沙雷菌的表型和基因数据。在 3 年期间,随机选择了 342 株临床肠杆菌科分离株进行 ESBL 产生检测,并评估了 bla(SHV)、bla(TEM)、bla(CTX-M)和 bla(TLA-1)β-内酰胺酶基因的存在情况。还测定了这些分离株的抗生素药敏性,并通过 PFGE 评估分离株的克隆性。根据我们的分析,92 株肺炎克雷伯菌中有 33 株(35.9%)、87 株阴沟肠杆菌中有 31 株(35.6%)、80 株大肠埃希菌中有 24 株(30%)和 83 株黏质沙雷菌中有 17 株(20.5%)被鉴定为 ESBL 产生菌。在 105 株分离株中有 99 株(94%)检测到 TEM、SHV 或 CTX ESBL 型。在 105 株分离株中均未检测到 TLA-1。优势 ESBL 型为 bla(SHV-5)(n=33)、bla(SHV12)(n=31)和 bla(CTX-M-15)(n=30)。E. coli 和阴沟肠杆菌分离株中主要的 ESBL 型是 CTX-M-15,而肺炎克雷伯菌和黏质沙雷菌中主要的类型分别是 SHV-12 和 SHV-5。PFGE 基因分型显示肺炎克雷伯菌分离株有两种主要的遗传模式,类型为 SHV-12 和 TEM-1+SHV-5。检测到由阴沟肠杆菌 SHV-5+CTX-M-15 引起的暴发。相比之下,大多数产 ESBL 的大肠埃希菌和黏质沙雷菌分离株没有类似的 PFGE 带型,因此遗传上并不相似。肠杆菌科在我院受到关注,尤其是肺炎克雷伯菌和阴沟肠杆菌。我们的结果证实 CTX-M-15 ESBL 型在医院中迅速传播,因此需要仔细监测。