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在普通变形杆菌中,blaNDM-1 碳青霉烯酶基因整合到一个新型的 SXT/R391 整合子-转座子上。

Integration of the blaNDM-1 carbapenemase gene into a novel SXT/R391 integrative and conjugative element in Proteus vulgaris.

机构信息

Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan Province, People's Republic of China.

Animal Disease Prevention and Food Safety Key Laboratory of Sichuan Province, Chengdu, People's Republic of China.

出版信息

J Antimicrob Chemother. 2020 Jun 1;75(6):1439-1442. doi: 10.1093/jac/dkaa068.

DOI:10.1093/jac/dkaa068
PMID:32155266
Abstract

OBJECTIVES

To characterize the genetic environment of the carbapenem resistance determinant in Proteus vulgaris of swine origin.

METHODS

The carbapenem-resistant P. vulgaris strain BC22 was isolated from a faecal swab from a diseased pig with diarrhoea in Sichuan Province of China in 2018. The presence of carbapenemase genes was screened by PCR. WGS and bioinformatics analysis were performed to analyse the genetic environment of the carbapenem resistance determinant.

RESULTS

P. vulgaris strain BC22 was found to harbour the carbapenemase gene blaNDM-1. WGS data revealed that blaNDM-1 was located in a truncated ISAba125 composite transposon. The carbapenem resistance gene blaNDM-1 and 20 other resistance genes, including the multiresistance gene cfr and the bifunctional aminoglycoside/quinolone resistance gene aac(6')-lb-cr, were located in a novel SXT/R391 integrative and conjugative element (ICE). This new SXT/R391 ICE of 148.7 kb was chromosomally located, and could be transferred to Escherichia coli.

CONCLUSIONS

Here, we report a carbapenemase gene, blaNDM-1, integrated into an SXT/R391 ICE. Our study highlights that this SXT/R391 ICE may facilitate the dissemination of clinically important resistance genes such as blaNDM-1, cfr and aac(6')-lb-cr.

摘要

目的

分析猪源普通变形杆菌碳青霉烯类耐药决定因子的遗传环境。

方法

2018 年,从中国四川省一头患有腹泻病的病猪粪便拭子中分离出一株碳青霉烯类耐药的普通变形杆菌 BC22 株。采用 PCR 筛选碳青霉烯酶基因。进行 WGS 和生物信息学分析,以分析碳青霉烯类耐药决定因子的遗传环境。

结果

发现普通变形杆菌 BC22 株携带碳青霉烯酶基因 blaNDM-1。WGS 数据显示,blaNDM-1 位于一个截断的 ISAba125 复合转座子中。碳青霉烯类耐药基因 blaNDM-1 和其他 20 个耐药基因,包括多耐药基因 cfr 和双功能氨基糖苷类/喹诺酮类耐药基因 aac(6')-lb-cr,位于一个新型 SXT/R391 整合子和可移动元件(ICE)中。这个新的 SXT/R391 ICE 大小为 148.7kb,位于染色体上,可以转移到大肠杆菌中。

结论

本研究报道了 blaNDM-1 碳青霉烯酶基因整合到 SXT/R391 ICE 中。我们的研究表明,这种 SXT/R391 ICE 可能促进 blaNDM-1、cfr 和 aac(6')-lb-cr 等临床重要耐药基因的传播。

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