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产碳青霉烯酶大肠埃希菌的毒力相关基因分析。

Virulence-associated genes analysis of carbapenemase-producing Escherichia coli isolates.

机构信息

Department of Microbiology, School of Medicine, Abadan University of Medical Sciences, Abadan, Iran.

Department of Biostatistics and Epidemiology, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

出版信息

PLoS One. 2022 May 10;17(5):e0266787. doi: 10.1371/journal.pone.0266787. eCollection 2022.

Abstract

Carbapenem-resistant Escherichia coli has emerged as a major public health issue across the world. This study was aimed to determine the virulence content and phylogenetic groups of carbapenemase-producing E. coli isolates in southwest Iran. One hundred and fifty-two non-duplicate E. coli isolates were collected from various clinical samples. Antibiotic susceptibility and minimum inhibitory concentrations (MIC) were determined according to the Clinical and Laboratory Standards Institute (CLSI) guidelines by Kirby-Bauer disc diffusion and agar dilution methods. Phenotypic screening of carbapenemase enzymes was performed by modified Hodge test (MHT). Detection of carbapenemase genes, phylogenetic groups, and virulence-associated genes were also performed by the PCR assay. The highest and lowest resistance rates were observed against mezlocillin (70.4%) and doripenem (13.1%), respectively. Out of 28 isolates that were resistant to carbapenem antibiotics, 12 (7.9%) strains were phenotypically carbapenemase producers. The blaOXA-48 was the predominant carbapenemase gene, detected in 58.3% of isolates, followed by blaIMP (41.7%) and blaNDM (8.3%). None of the isolates harbored blaVIM and blaKPC genes. Among the twelve carbapenemase-producing strains, urinary isolates were mostly classified into B2 (41.7%) and D (25%) phylogenetic groups, while other clinical isolates belonged to B1 (25%) and A (8.3%) groups. The frequency of virulence-associated genes was also investigated in all isolates and ranged from 6.6% for hly to 75% for fimA. The emergence of carbapenemase-producing strains is a growing concern to public health. Therefore, the proper implementation of monitoring programs is crucial for limiting their dissemination.

摘要

碳青霉烯类耐药大肠杆菌已成为全球主要的公共卫生问题。本研究旨在确定伊朗西南部产碳青霉烯酶大肠杆菌分离株的毒力含量和系统发育群。从各种临床标本中采集了 152 株非重复大肠杆菌分离株。根据临床和实验室标准协会(CLSI)指南,采用 Kirby-Bauer 纸片扩散和琼脂稀释法测定抗生素敏感性和最小抑菌浓度(MIC)。采用改良 Hodge 试验(MHT)进行碳青霉烯酶表型筛选。采用 PCR 法检测碳青霉烯酶基因、系统发育群和毒力相关基因。对美洛西林(70.4%)和多利培南(13.1%)的耐药率最高和最低。在 28 株对碳青霉烯类抗生素耐药的分离株中,有 12 株(7.9%)为表型碳青霉烯酶产生菌。blaOXA-48 是最主要的碳青霉烯酶基因,在 58.3%的分离株中检出,其次是 blaIMP(41.7%)和 blaNDM(8.3%)。没有分离株携带 blaVIM 和 blaKPC 基因。在 12 株产碳青霉烯酶的菌株中,尿分离株主要分为 B2(41.7%)和 D(25%)系统发育群,而其他临床分离株属于 B1(25%)和 A(8.3%)群。还对所有分离株进行了毒力相关基因的频率调查,从 hly 的 6.6%到 fimA 的 75%不等。产碳青霉烯酶菌株的出现对公共卫生构成了越来越大的威胁。因此,正确实施监测计划对于限制其传播至关重要。

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