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临床分离株中携带IncFII质粒和(A)变体的分子特征分析。

Molecular Characterization of an IncFII Plasmid Co-harboring and (A) Variant in a Clinical Isolate.

作者信息

Yao Hong, Cheng Jing, Li Aijuan, Yu Runhao, Zhao Wenbo, Qin Shangshang, Du Xiang-Dang

机构信息

College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.

School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, China.

出版信息

Front Microbiol. 2020 Jul 24;11:1610. doi: 10.3389/fmicb.2020.01610. eCollection 2020.

Abstract

Carbapenems and tigecycline are two important classes of antimicrobial agents to treat the infections caused by Enterobacterales. Here, we reported a plasmid carrying both and (A) variant in clinical KP-1572. MIC results showed that KP-1572 was resistant to a wide range of antimicrobials. The and (A) variant were located on an identical plasmid, which was indicated by S1-PFGE and southern blotting hybridization and can be successfully transferred by electroporation. Whole-plasmid sequencing and analysis revealed that a 142,993-bp-sized plasmid, designated pIMP1572, contains an IncFII backbone and a variable region harboring and (A) variant. The plasmid pIMP1572 was apparently originated from a (A)-carrying IncFII plasmid but with a deletion length of 6,216-bp and a multiple drug resistance region (MDRR) insertion of 25,259 bp. The plasmid pIMP1572 in the present study represents the first report of the IncFII plasmid co-carrying and (A) variant, which should be monitored.

摘要

碳青霉烯类和替加环素是治疗肠杆菌科细菌引起感染的两类重要抗菌药物。在此,我们报道了临床分离的肺炎克雷伯菌KP-1572中携带blaKPC和blaNDM-1(A)变体的一个质粒。最小抑菌浓度(MIC)结果显示,KP-1572对多种抗菌药物耐药。blaKPC和blaNDM-1(A)变体位于同一个质粒上,这通过S1-PFGE和Southern杂交得以证实,并且该质粒可通过电穿孔成功转移。全质粒测序及分析表明,一个大小为142,993 bp的质粒,命名为pIMP1572,含有一个IncFII骨架和一个携带blaKPC和blaNDM-1(A)变体的可变区。质粒pIMP1572显然起源于一个携带blaNDM-1(A)的IncFII质粒,但有一个6,216 bp的缺失和一个25,259 bp的多重耐药区域(MDRR)插入。本研究中的质粒pIMP1572是首次报道的同时携带blaKPC和blaNDM-1(A)变体的IncFII质粒,应对其进行监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab1/7393768/824f831388c2/fmicb-11-01610-g001.jpg

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