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土耳其出现产碳青霉烯酶和多粘菌素耐药肺炎克雷伯菌 ST101 高危克隆。

Emergence of carbapenemase-producing and colistin resistant Klebsiella pneumoniae ST101 high-risk clone in Turkey.

机构信息

1Department of Medical Microbiology, Faculty of Medicine, Hacettepe University, 06100, Ankara, Turkey.

2Department of Microbiology, Faculty of Molecular Biology and Genetics, Usak University, 64200, Usak, Turkey.

出版信息

Acta Microbiol Immunol Hung. 2020 Nov 9;67(4):216-221. doi: 10.1556/030.2020.01275.

DOI:10.1556/030.2020.01275
PMID:33174866
Abstract

Carbapenemase-producing and colistin resistant Klebsiella pneumoniae has become a worldwide healthcare problem. This study describes molecular characterization of carbapenemase-producing and colistin resistant clinical K. pneumoniae isolates.A total of 93 non-replicate carbapenem and colistin resistant K. pneumoniae were recovered from clinical specimens in a university hospital during 2017-2019. Detection of blaOXA-48, blaKPC, blaNDM-1, blaIMP, blaVIM-1 and mcr-1, -2, -3, -4, -5, -6, -7, and -8 genes was performed by PCR. The bacterial isolates were assigned to clonal lineages by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST).All isolates harbored blaOXA-48 and only two isolates harbored blaOXA-48, and blaNDM-1 genes together. In colistin resistant K. pneumoniae, mcr-1 was detected in two (2.1%) isolates. Ninety three isolates of K. pneumoniae were categorized into three clusters and five pulsotypes. MLST revealed two different sequence types, ST101 (89/93) and ST147 (4/93).In our study ST101 was found to be a significantly dominant clone carrying blaOXA-48 and among our strains a low frequency of mcr-1 gene was determined. The emergence of colistin resistance was observed in K. pneumoniae ST101 isolates. ST101 may become a global threat in the dissemination of carbapenem and colistin resistance.

摘要

产碳青霉烯酶和多黏菌素耐药肺炎克雷伯菌已成为全球卫生保健问题。本研究描述了产碳青霉烯酶和多黏菌素耐药临床肺炎克雷伯菌分离株的分子特征。

2017 年至 2019 年,从一所大学医院的临床标本中分离出 93 株非重复碳青霉烯类和多黏菌素类耐药肺炎克雷伯菌。通过 PCR 检测 blaOXA-48、blaKPC、blaNDM-1、blaIMP、blaVIM-1 和 mcr-1、-2、-3、-4、-5、-6、-7 和 -8 基因。通过脉冲场凝胶电泳(PFGE)和多位点序列分型(MLST)对细菌分离株进行克隆谱系分析。

所有分离株均携带 blaOXA-48 基因,只有两株同时携带 blaOXA-48 和 blaNDM-1 基因。在多黏菌素耐药肺炎克雷伯菌中,有 2 株(2.1%)检测到 mcr-1 基因。93 株肺炎克雷伯菌分为 3 个聚类和 5 个脉冲型。MLST 显示两种不同的序列类型,ST101(89/93)和 ST147(4/93)。

在本研究中,ST101 被发现是一种携带 blaOXA-48 的优势克隆,在我们的菌株中,mcr-1 基因的频率较低。在肺炎克雷伯菌 ST101 分离株中观察到多黏菌素耐药的出现。ST101 可能成为碳青霉烯类和多黏菌素类耐药传播的全球威胁。

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