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首页> 外文期刊>Veterinary Microbiology >Prevalence of plasmid-mediated quinolone resistance qnr genes in poultry and swine clinical isolates of Escherichia coli
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Prevalence of plasmid-mediated quinolone resistance qnr genes in poultry and swine clinical isolates of Escherichia coli

机译:质粒介导的喹诺酮耐药qnr基因在大肠杆菌的家禽和猪临床分离株中的流行

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摘要

The prevalence of qnr genes was investigated in veterinary clinical isolates of Escherichia coli in Guangdong province, China, and the aac (6')-Ib gene and the mutations in QRDRs of gyrase and topoisomerase IV were examined in qnr-positive strains. A total of 232 E. coli strains isolated from pig and poultry were screened for the presence of the qnrA, qnrB and qnrS genes by PCR and sequencing. The aac (6')-Ib gene was detected in qnr-bearing strains by PCR and sequencing. For all strains carrying qnr, MICs for six quinolones were determined. Mutations within the gyrase and topoisomerase were analyzed by PCR and sequencing for all the QRDRs of gyrA, gyrB, parC and parE. Among 232 E. coli isolates, 14 (6%) isolates were positive for the qnr gene, including one for qnrB, 13 for qnrS, but no qnrA was identified in this population. Detection of the aac (6')-Ib gene showed that one qnrS-positive isolate from pig and one qnrB-positive isolate from duck carried aac (6')-Ib gene, and both were the cr variant allele of aac (6')-Ib. All of the 14 isolates had MICs of ciprofloxacin more than 0.25 mg/L. Mutations in the QRDR of gyrA mutations were observed in 5 (35.7%) of the 14 strains. Three fluoroquinolone-resisting strains showed one mutation S83L of gyrA, while one S83I. One high-level resistance strains harboured gyrA S83L and A87N of gyrA. A singe mutation in site 58 of parC was detected in 3 (21.4%) strains. None mutations were found in QRDRs of gyrB and parE. The emergence of qnr genes in veterinary clinical E. coli isolates is described for the first time. This is also the first report of aac (6')-Ib-cr gene in E. coli isolates from food-producing animals.
机译:在中国广东省的兽医临床分离株中调查了qnr基因的患病率,并在qnr阳性菌株中检查了aac(6')-Ib基因以及回旋酶和拓扑异构酶IV的QRDR突变。通过PCR和测序,从猪和家禽中分离出总共232株大肠杆菌,筛选出qnrA,qnrB和qnrS基因的存在。通过PCR和测序在携带qnr的菌株中检测到aac(6')-Ib基因。对于所有携带qnr的菌株,确定了六个喹诺酮类药物的MIC。通过PCR和测序分析了gyrA,gyrB,parC和parE的所有QRDR中的促旋酶和拓扑异构酶内的突变。在232株大肠杆菌中,qnr基因呈阳性,其中14株为阳性,其中qnrB为1株,qnrS为13株,但在此人群中未鉴定出qnrA。对aac(6')-Ib基因的检测表明,来自猪的1个qnrS阳性分离株和来自鸭肉的1个qnrB阳性分离株均携带aac(6')-Ib基因,均为aac(6' )-Ib。 14个分离株的所有环丙沙星的MIC均大于0.25 mg / L。在14个菌株中的5个(35.7%)中观察到了gyrA突变的QRDR突变。 3株耐氟喹诺酮菌株显示了一个gyrA突变S83L,而一个S83I突变。一株高水平抗性菌株包含gyrA的gyrA S83L和A87N。在3个(21.4%)菌株中检测到parC 58位的单基因突变。在gyrB和parE的QRDR中未发现突变。首次描述了兽医临床大肠杆菌分离物中qnr基因的出现。这也是来自产食动物的大肠杆菌分离物中aac(6')-Ib-cr基因的首次报道。

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