Molecular Biology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran.
Microb Pathog. 2020 Dec;149:104507. doi: 10.1016/j.micpath.2020.104507. Epub 2020 Sep 17.
Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKp) has been increasingly reported and is now recognized as a public health concern. The aim of this study was to investigate the molecular epidemiology of CR-hvKp strains that were isolated from an Iranian hospital. A total of 74 non-duplicated carbapenem-resistant K. pneumoniae (CR-Kp) were collected from patients' clinical or surveillance cultures. Resistance/virulence genes were identified by PCR and sequencing. String test, capsular genotyping, conjugation assays, PCR-based replicon typing, pulsed field gel electrophoresis (PFGE), multilocus sequence typing (MLST) and were performed. All 74 CR-Kp isolates were carbapenemase producers, which co-carried multiple resistance genes such as bla, bla, bla, qnrB1, and qnrS1. The most common carbapenemase gene was bla (67/74 90.5%), followed by bla (18/74 24.3%), and bla (3/74 4%). The bla and bla were found on IncL/M and IncFII conjugative plasmids, respectively. Of 74 CR-Kp isolates, 49 were positive for string test. Capsular genotyping revealed that 34 and 10 CR-Kp strains belonged to the K1 and K2 serotypes, respectively. rmpA was the most prevalent virulence gene detected in 64.8% of the isolates. Fifty two strains were identified as CR-hvKp. PFGE typing showed 5 different clusters with two major clusters B (39 isolates, 52.7%) associated with sequence type 11 (ST11), and A (21 isolates, 28.4%) associated with ST893. Furthermore, ST147, ST392, and ST15 carbapenemase producers have also been sporadically identified. One isolate belonging to ST11 was resistant to colistin and were negative for mcr-1-2-3 genes. Insertional inactivation of mgrB due to IS elements was observed in the colistin-resistant isolate. Our findings suggest that ST11 CR-hvKP strain has a clonal distribution in our hospital. Therefore, immediate implementation of infection-control measures may be the best way to prevent the spread of these clones.
耐碳青霉烯类超毒力肺炎克雷伯菌 (CR-hvKp) 的报道越来越多,现已被认为是公共卫生关注的问题。本研究旨在调查从伊朗一家医院分离的耐碳青霉烯类超毒力肺炎克雷伯菌 (CR-hvKp) 菌株的分子流行病学。从患者的临床或监测培养物中收集了 74 株非重复耐碳青霉烯类肺炎克雷伯菌 (CR-Kp)。通过 PCR 和测序鉴定耐药/毒力基因。进行了 String 试验、荚膜基因分型、接合试验、基于 PCR 的复制子分型、脉冲场凝胶电泳 (PFGE)、多位点序列分型 (MLST)。74 株 CR-Kp 分离株均为碳青霉烯酶产生菌,同时携带 bla、bla、bla、qnrB1 和 qnrS1 等多种耐药基因。最常见的碳青霉烯酶基因是 bla(67/74,90.5%),其次是 bla(18/74,24.3%)和 bla(3/74,4%)。bla 和 bla 分别位于 IncL/M 和 IncFII 可接合质粒上。74 株 CR-Kp 分离株中,49 株 String 试验阳性。荚膜基因分型显示,34 株和 10 株 CR-Kp 菌株分别属于 K1 和 K2 血清型。rmpA 是 64.8%分离株中检测到的最普遍的毒力基因。52 株被鉴定为 CR-hvKp。PFGE 分型显示有 5 个不同的簇,其中 2 个主要簇 B(39 株,52.7%)与 ST11 相关,A(21 株,28.4%)与 ST893 相关。此外,还偶尔鉴定出 ST147、ST392 和 ST15 碳青霉烯酶产生菌。一株属于 ST11 的分离株对多粘菌素耐药,mcr-1-2-3 基因阴性。在多粘菌素耐药分离株中观察到由于 IS 元件导致的 mgrB 插入失活。我们的研究结果表明,ST11 CR-hvKP 菌株在我院具有克隆分布。因此,立即实施感染控制措施可能是防止这些克隆传播的最佳方法。