首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >High Prevalence of Plasmid-Mediated Quinolone Resistance Determinants qnr aac(6′)-Ib-cr and qepA among Ceftiofur-Resistant Enterobacteriaceae Isolates from Companion and Food-Producing Animals
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High Prevalence of Plasmid-Mediated Quinolone Resistance Determinants qnr aac(6′)-Ib-cr and qepA among Ceftiofur-Resistant Enterobacteriaceae Isolates from Companion and Food-Producing Animals

机译:在伴生动物和食物生产动物中耐头孢噻呋的肠杆菌科细菌中质粒介导的喹诺酮抗性决定簇qnraac(6)-Ib-cr和qepA普遍存在

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摘要

Three kinds of plasmid-mediated quinolone resistance (PMQR) determinants have been discovered and have been shown to be widely distributed among clinical isolates: qnr genes, aac(6′)-Ib-cr, and qepA. Few data on the prevalence of these determinants in strains from animals are available. The presence of PMQR genes in isolates from animals was determined by PCR amplification and DNA sequencing. The production of extended-spectrum β-lactamases (ESBLs) and AmpC β-lactamases in the strains was detected, and their genotypes were determined. The genetic environment of PMQR determinants in selected plasmids was analyzed. All samples of ceftiofur-resistant (MICs ≥ 8 μg/ml) isolates of the family Enterobacteriaceae were selected from 36 companion animals and 65 food-producing animals in Guangdong Province, China, between November 2003 and April 2007, including 89 Escherichia coli isolates, 9 Klebsiella pneumoniae isolates, and isolates of three other genera. A total of 68.3% (69/101) of the isolates produced ESBLs and/or AmpC β-lactamases, mainly those of the CTX-M and CMY types. Of the 101 strains, PMQR determinants were present in 35 (34.7%) isolates, with qnr, aac(6′)-Ib-cr, and qepA detected alone or in combination in 8 (7.9%), 19 (18.8%), and 16 (15.8%) strains, respectively. The qnr genes detected included one qnrB4 gene, four qnrB6 genes, and three qnrS1 genes. Five strains were positive for both aac(6′)-Ib-cr and qepA, while one strain was positive for qnrS1, aac(6)-Ib-cr, and qepA. qnrB6 was flanked by two copies of ISCR1 with an intervening dfr gene downstream and sul1 and qacEΔ1 genes upstream. In another plasmid, aac(6)-Ib-cr followed intI1 and arr-3 was downstream. PMQR determinants are highly prevalent in ceftiofur-resistant Enterobacteriaceae strains isolated from animals in China. This is the first report of the occurrence of PMQR determinants among isolates from companion animals.
机译:已发现三种质粒介导的喹诺酮抗药性(PMQR)决定簇,并已表明它们广泛分布于临床分离株中:qnr基因,aac(6')-Ib-cr和qepA。目前尚缺乏有关这些决定因素在动物品系中普遍存在的数据。通过PCR扩增和DNA测序确定动物分离物中PMQR基因的存在。检测菌株中广谱β-内酰胺酶(ESBLs)和AmpCβ-内酰胺酶的产生,并确定其基因型。分析了所选质粒中PMQR决定簇的遗传环境。从2003年11月至2007年4月间,从中国广东省的36只伴侣动物和65只食用动物中选取了所有肠杆菌科的耐头孢噻呋(MICs≥8μg/ ml)分离株,包括89株大肠杆菌, 9株肺炎克雷伯菌分离株,以及其他三个属的分离株。共有68.3%(69/101)的分离物产生ESBL和/或AmpCβ-内酰胺酶,主要是CTX-M和CMY类型的。在101个菌株中,PMQR决定子存在于35个(34.7%)分离株中,其中qnr,aac(6')-Ib-cr和qepA单独或组合检测到的有8(7.9%),19(18.8%)个,和16(15.8%)株。检测到的qnr基因包括一个qnrB4基因,四个qnrB6基因和三个qnrS1基因。 5株aac(6')-Ib - cr qepA 均为阳性,而1株 qnrS1阳性, aac(6 ')-Ib - cr qepA。 qnrB6 的两侧是IS CR1 的两个副本,中间有一个 dfr 基因,下游是 sul1 qacE Δ 1 基因上游。在另一个质粒中, aac(6 ')-Ib-cr 随后是 intI1 ,而 arr-3 在下游。 PMQR决定簇在从中国动物体内分离出来的对头孢噻呋耐药的 Enterobacteriaceae 菌株中非常普遍。这是关于伴生动物分离物中PMQR决定簇发生的首次报道。

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