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Prevalence and Characteristics of Extended-Spectrum β-Lactamase and Plasmid-Mediated Fluoroquinolone Resistance Genes in Escherichia coli Isolated from Chickens in Anhui Province China

机译:安徽省鸡分离大肠埃希菌中广谱β-内酰胺酶和质粒介导的氟喹诺酮耐药基因的流行和特征

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摘要

The aim of this study was to characterize the prevalence of extended-spectrum β-lactamase (ESBL) genes and plasmid-mediated fluoroquinolone resistance (PMQR) determinants in 202 Escherichia coli isolates from chickens in Anhui Province, China, and to determine whether ESBL and PMQR genes co-localized in the isolates. Antimicrobial susceptibility for 12 antimicrobials was determined by broth microdilution. Polymerase chain reactions (PCRs), DNA sequencing, and pulsed field gel electrophoresis (PFGE) were employed to characterize the molecular basis for β-lactam and fluoroquinolone resistance. High rates of antimicrobial resistance were observed, 147 out of the 202 (72.8%) isolates were resistant to at least 6 antimicrobial agents and 28 (13.9%) of the isolates were resistant to at least 10 antimicrobials. The prevalence of bla CTX-M, bla TEM-1 and bla TEM-206 genes was 19.8%, 24.3% and 11.9%, respectively. Seventy-five out of the 202 (37.1%) isolates possessed a plasmid-mediated quinolone resistance determinant in the form of qnrS (n = 21); this determinant occurred occasionally in combination with aac(6′)-1b-cr (n = 65). Coexistence of ESBL and/or PMQR genes was identified in 31 of the isolates. Two E. coli isolates carried bla TEM-1, bla CTX-M and qnrS, while two others carried bla CTX-M, qnrS and aac(6′)-1b-cr. In addition, bla TEM-1, qnrS and aac(6′)-1b-cr were co-located in two other E. coli isolates. PFGE analysis showed that these isolates were not clonally related and were genetically diverse. To the best of our knowledge, this study is the first to describe detection of TEM-206-producing E. coli in farmed chickens, and the presence of bla TEM-206, qnrS and aac(6′)-1b-cr in one of the isolates.
机译:这项研究的目的是表征在中国安徽省鸡群的202株大肠杆菌中超广谱β-内酰胺酶(ESBL)基因和质粒介导的氟喹诺酮耐药性(PMQR)决定因素的流行情况,并确定ESBL和PMQR基因共定位在分离物中。通过肉汤微量稀释确定对12种抗菌药的抗菌药敏性。聚合酶链反应(PCR),DNA测序和脉冲场凝胶电泳(PFGE)用于表征β-内酰胺和氟喹诺酮耐药性的分子基础。观察到高耐药率,在202株分离菌中有147株(72.8%)对至少6种抗菌剂有耐药性,在28株分离菌中(13.9%)对至少10种抗菌剂有耐药性。 bla CTX-M,bla TEM-1和bla TEM-206基因的患病率分别为19.8%,24.3%和11.9%。 202个分离株中有75个(占37.1%)具有qnrS形式的质粒介导的喹诺酮抗性决定簇(n = 21)。该决定因素偶尔与aac(6')-1b-cr结合出现(n = 65)。 ESBL和/或PMQR基因共存于31个分离株中。两个大肠杆菌分离株携带bla TEM-1,bla CTX-M和qnrS,而另外两个大肠杆菌分离株则携带bla CTX-M,qnrS和aac(6')-1b-cr。此外,bla TEM-1,qnrS和aac(6')-1b-cr共同位于另外两个 E中。大肠杆菌分离株。 PFGE分析表明,这些分离株没有克隆关系,并且遗传多样。据我们所知,这项研究是第一个描述检测产生TEM-206的 E的研究。鸡中的大肠杆菌以及 bla TEM-206, qnrS aac(6')-1b-cr 的存在在其中一种分离物中。

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