Identification of an IncHI5-like plasmid co-harboring bla NDM-1 and bla OXA-1 in mcr-8.1-positive Klebsiella pneumoniae isolate.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-05-27 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1601035
Xu Liu, Tingting Zhang, Zhiyang Yu, Shangshang Qin, Muchen Zhang, Yan Li
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引用次数: 0

Abstract

The emergence of polymyxin-resistant carbapenem-resistant Klebsiella pneumoniae (CRKP) severely limits clinical treatment options and poses a significant threat to anti-infective therapy. In this study, we investigated the genetic characteristics of an IncHI5-like plasmid co-harboring bla NDM-1 and bla OXA-1 in an mcr-8.1-positive clinical CRKP isolate using a combination of MIC testing, conjugation experiments, bacterial whole-genome sequencing, and bioinformatics analyses. The ST626 CRKP strain KP19-2581, isolated from a human clinical infection, exhibited a multidrug-resistant (MDR) phenotype. Whole-genome sequencing revealed that the colistin resistance gene mcr-8.1 was located on an IncFIA/IncFII plasmid, flanked by the conserved structure IS903B-orf-mcr-8.1-orf-IS903B. In addition, strain KP19-2581 carried a novel IncHI5-like MDR plasmid, designated pKP19-2581-367k-HI5-NDM1, which co-harbored the bla NDM-1 and bla OXA-1 genes. This plasmid contained two MDR regions, harboring a diverse array of resistance genes across multiple antibiotic classes. The dissemination of bla OXA-1 in variable region is related to the structure of class 1 integron, while IS26 mediates the integration of bla NDM-1 on IncHI5-like plasmid. Notably, this is the first report of an IncHI5-like plasmid carrying both bla NDM-1 and two copies of bla OXA-1, along with multiple resistance genes and insertion sequences. Given its potential to acquire additional resistance determinants, this plasmid may serve as a reservoir for further antimicrobial resistance evolution, underscoring the urgent need for surveillance of IncHI5 plasmids to mitigate their clinical and epidemiological impact.

mcr-8.1阳性肺炎克雷伯菌分离株中含有bla NDM-1和bla OXA-1的inchi5样质粒的鉴定
耐多粘菌素碳青霉烯耐药性肺炎克雷伯菌(CRKP)的出现严重限制了临床治疗选择,并对抗感染治疗构成重大威胁。在这项研究中,我们利用MIC检测、偶联实验、细菌全基因组测序和生物信息学分析,研究了mcr-8.1阳性临床CRKP分离物中含有bla NDM-1和bla OXA-1的inchi5样质粒的遗传特性。ST626 CRKP菌株KP19-2581从人类临床感染中分离出来,表现出多药耐药表型。全基因组测序结果显示,耐粘菌素基因mcr-8.1位于IncFIA/IncFII质粒上,两侧为保守结构IS903B-orf-mcr-8.1-orf-IS903B。此外,菌株KP19-2581携带一种新的inchi5样MDR质粒,命名为pKP19-2581-367k-HI5-NDM1,该质粒共含bla NDM-1和bla OXA-1基因。该质粒包含两个耐多药区域,包含多种抗生素类的多种耐药基因。bla OXA-1在可变区域的传播与1类整合子的结构有关,而IS26介导bla NDM-1在inchi5样质粒上的整合。值得注意的是,这是首次报道携带bla NDM-1和两个bla OXA-1拷贝的inchi5样质粒,以及多个抗性基因和插入序列。鉴于其获得额外耐药决定因素的潜力,该质粒可能作为进一步抗菌素耐药性进化的储存库,强调迫切需要对IncHI5质粒进行监测,以减轻其临床和流行病学影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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