Serotyping of Escherichia coli species isolated from broilers and determination of Colistin resistance

U. Parın, Gonenc Simsek
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Abstract

Systemic infections by avian pathogenic Escherichia coli (APEC) are economically damaging to poultry industries Worldwide. E. coli strains of serotypes O1, O2, O18 and O78 are preferentially associated with avian colibacillosis. The rfb gene cluster that controls O antigen synthesis generally varies among different E. coli serotypes. In this study, the rfb gene clusters of E. coli serotypes O1, O2, O18 and O78 were characterized and compared, and it was also aimed to search for Colistin resistance on a molecular basis. For the research, 200 swab samples were taken from 200 chickens suspected of colibacillosis in broiler poultry farms located in the vicinity of Aydın, İzmir, and Manisa Provinces in Turkey 2022. Bacterial growth was obtained from 92% of the samples, and microbiological analysis identified 108 (54%) Escherichia coli isolates. In addition, Klebsiella spp. was identified in 35 (17.5%) samples, Proteus spp. in 23 (11.5%), Pseudomonas spp. in 18 (9%), and no bacterial growth was observed in 16 (8%) samples. mcr-1 (309 bp) and mcr–2 (567 bp) genes responsible for Colistin resistance was investigated in plasmid DNA extracted from 108 E. coli isolates obtained in the study, using the PCR method. However, neither mcr-1 nor mcr–2 genes were detected in any of the samples. In conclusion, the allele-specific PCR method was found sensitive and applicable for APEC identification and multiple drug resistance emerged in E. coli strains isolated according to the antibiogram results.
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肉鸡分离大肠埃希菌的血清分型及粘菌素耐药性测定
禽致病性大肠杆菌(APEC)的全身性感染对世界范围内的家禽业造成了经济上的损害。大肠杆菌菌株血清型O1、O2、O18和O78与禽大肠杆菌病优先相关。控制O抗原合成的rfb基因簇通常在不同的大肠杆菌血清型中有所不同。本研究对大肠杆菌O1、O2、O18和O78血清型的rfb基因簇进行了表征和比较,并从分子基础上寻找粘菌素耐药性。在这项研究中,从位于土耳其2022年Aydın、İzmir和马尼萨省附近的肉鸡养殖场的200只疑似大肠杆菌病的鸡身上采集了200个拭子样本。92%的样品有细菌生长,微生物学分析鉴定出108株(54%)大肠杆菌。检出克雷伯氏菌35株(17.5%),变形杆菌23株(11.5%),假单胞菌18株(9%),16株(8%)未见细菌生长。从108株大肠杆菌分离株中提取质粒DNA,采用PCR方法对与粘菌素耐药相关的mcr-1 (309 bp)和mcr-2 (567 bp)基因进行检测。然而,在所有样本中均未检测到mcr-1和mcr-2基因。综上所述,等位基因特异性PCR方法对APEC鉴定是敏感和适用的,根据抗生素谱结果,分离的大肠杆菌菌株出现了多重耐药。
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18 weeks
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