Chen Yisheng, Gao Jing, Zhang Haomin, Ying Chunmei
Department of Clinical Laboratory, Obstetrics and Gynecology Hospital of Fudan University Shanghai, China.
Department of Clinical Laboratory, Renji Hospital, Shanghai Jiao Tong University School of Medicine Shanghai, China.
Front Microbiol. 2017 Feb 6;8:163. doi: 10.3389/fmicb.2017.00163. eCollection 2017.
The rapid expansion of carbapenem-resistant (CRAB) clinical isolates is a big issue. We investigated the antibiotic susceptibility, molecular epidemiology and resistance gene of collected at two hospitals in Shanghai, China. Besides, the PCR-based replicon typing method (AB-PBRT) was conducted to categorize the plasmids into homogeneous groups on the basis of replicase genes. Most CRAB isolates showed high-level resistance to almost all antibiotics but retain susceptibility to colistin and tigecycline. A total of 101 isolates carried -like gene. Sequencing identified the presence of for CRAB isolates. gene were discovered in all CRAB isolates. Each CRAB isolate contained 1-3 of 19 different plasmid replicase () gene homology groups (GRs) and the GR6 (Aci6) was ubiquitous. Genotyping by Multilocus Sequence Typing (MLST) showed seven defined MLST patterns and three novel STs were found. eBURST analysis indicated they were all grouped in CC92 (GCII) with the most frequent ST208 (50%). Two -bearing transposons were found: Tn and Tn. Tn were detected in 54 (96.4%) isolates and Tn in two remaining isolates. The carbapenem gene was vitally associated with Aci6 plasmid belong to CC92 clonal group. Our survey revealed severe drug resistance in isolates. Tn-containing CC92 were endemic, which may facilitate the dissemination.
耐碳青霉烯类鲍曼不动杆菌(CRAB)临床分离株的迅速增多是一个重大问题。我们对在中国上海两家医院收集的CRAB进行了抗生素敏感性、分子流行病学及耐药基因研究。此外,采用基于PCR的复制子分型方法(AB-PBRT),根据复制酶基因将质粒分类为同源组。多数CRAB分离株对几乎所有抗生素呈现高水平耐药,但对黏菌素和替加环素仍敏感。共有101株分离株携带blaOXA-23-like基因。测序确定了CRAB分离株blaOXA-23基因的存在。所有CRAB分离株均发现blaOXA-51-like基因。每株CRAB分离株含有19种不同质粒复制酶(rep)基因同源组(GRs)中的1-3种,GR6(Aci6)最为常见。多位点序列分型(MLST)基因分型显示有7种确定的MLST型,还发现了3种新的序列型(STs)。eBURST分析表明,它们都归为CC92(GCII)克隆群,最常见的是ST208(50%)。发现了两种携带blaOXA-23的转座子:Tn2006和Tn1999。54株(96.4%)分离株检测到Tn2006,其余2株分离株检测到Tn1999。blaOXA-23碳青霉烯酶基因与属于CC92克隆群的Aci6质粒密切相关。我们的调查揭示了CRAB分离株的严重耐药情况。含Tn2006的CC92克隆群呈地方性流行,这可能促进了blaOXA-23的传播。