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中国山东大肠杆菌分离株中质粒介导氟喹诺酮耐药基因的调查及其传播。

A survey of plasmid-mediated fluoroquinolone resistance genes from Escherichia coli isolates and their dissemination in Shandong, China.

机构信息

Key Laboratory of Development and Evaluation of the Chemical and Herbal Drugs for Animal Use, National Center for Veterinary Drug Safety Evaluation, College of Veterinary Medicine, China Agricultural University, Beijing, China.

出版信息

Foodborne Pathog Dis. 2010 Feb;7(2):207-15. doi: 10.1089/fpd.2009.0378.

Abstract

Bacterial resistance to fluoroquinolones result from mutations in the quinolone resistance-determining regions of the drug targets, overexpression of efflux pumps, and/or the more recently identified plasmid-mediated low-level resistance mechanisms. We investigated the prevalence of and characterized plasmid-mediated fluoroquinolone resistance genes (qnrA, qnrB, qnrS, aac(6')-Ib-cr, and qepA) by polymerase chain reaction in fluoroquinolone-resistant Escherichia coli (n = 530) isolated from a chicken farm, a pig farm, and hospitalized patients in Shandong, China, in 2007. The aac(6')-Ib-cr gene was the most prevalent resistance gene that was detected in bacteria isolated from all sources. Next was the qnrS gene, which was predominantly present in isolates from the pig farm. Only eight (5.8%) isolates from hospital patients were found to possess the qepA gene, and these isolates were first reported in qepA-carrying E. coli from humans in China. The qnrA and qnrB genes were not detected in any of the isolates. Further, most of the isolates were also resistant to beta-lactams and aminoglycosides as determined by the broth microdilution method. Pulsed-field gel electrophoresis analysis of the E. coli isolates with similar resistance patterns that also carried resistance genes showed great genomic diversity among these bacteria, suggesting that the multiresistant E. coli isolates carrying the qnr, aac(6')-Ib-cr, or qepA genes were not derived from a specific clone, but represented a wide variety of different genotypes. The results of Southern hybridization revealed that qepA, qnrS, and parts of aac(6')-Ib-cr genes were localized on plasmids and/or chromosome. qepA and aac(6')-Ib-cr genes were colocalized with aac(6')-Ib-cr and qnrS genes, respectively, on the same plasmids. Our study demonstrated that two different genes (qepA and aac(6')-Ib-cr) were identified on the same plasmid in E. coli strains derived from patients and qnrS and aac(6')-lb-cr genes on the same plasmid in an E. coli strain of animal origin.

摘要

细菌对氟喹诺酮类药物的耐药性是由于药物靶标中的喹诺酮类耐药决定区发生突变、外排泵过度表达以及/或者最近发现的质粒介导的低水平耐药机制所致。我们通过聚合酶链反应,调查了质粒介导的氟喹诺酮耐药基因(qnrA、qnrB、qnrS、aac(6')-Ib-cr 和 qepA)在中国山东的一个养鸡场、一个养猪场和住院患者中分离的 530 株耐氟喹诺酮的大肠埃希菌(Escherichia coli)中的流行情况并对其进行了特征描述。在所研究的细菌中,aac(6')-Ib-cr 基因是最常见的耐药基因,它可从所有来源的细菌中检测到。其次是 qnrS 基因,它主要存在于来自养猪场的分离株中。仅从医院患者中分离的 8 株(5.8%)细菌中发现携带 qepA 基因,这是首次在中国人类携带 qepA 的大肠埃希菌中报告的。在任何分离株中都未检测到 qnrA 和 qnrB 基因。此外,通过肉汤微量稀释法测定,大多数分离株还对β-内酰胺类和氨基糖苷类药物具有耐药性。对具有相似耐药模式且携带耐药基因的大肠埃希菌分离株进行脉冲场凝胶电泳分析显示,这些细菌具有很大的基因组多样性,表明携带 qnr、aac(6')-Ib-cr 或 qepA 基因的多耐药大肠埃希菌分离株并非来自特定的克隆,而是代表了广泛不同的基因型。Southern 杂交的结果显示,qepA、qnrS 和部分 aac(6')-Ib-cr 基因定位于质粒和/或染色体上。qepA 和 aac(6')-Ib-cr 基因分别与 qnrS 和 aac(6')-Ib-cr 基因共定位在同一质粒上。我们的研究表明,在来自患者的大肠埃希菌菌株中发现了两个不同的基因(qepA 和 aac(6')-Ib-cr)定位于同一质粒上,在来自动物的大肠埃希菌菌株中发现了 qnrS 和 aac(6')-lb-cr 基因定位于同一质粒上。

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