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Phylogenetic typing and molecular detection of virulence factors of avian pathogenic Escherichia coli isolated from colibacillosis cases in Japanese quail

机译:日本鹌鹑大肠埃希菌病病例分离的禽致病性大肠杆菌的系统发育分型和毒力因子的分子检测

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摘要

Colibacillosis caused by avian pathogenic Escherichia coli (APEC) is an economic threat to the poultry industry throughout the world. Some of the virulence genes may enhance the ability of E. coli isolates to grow in the tissues of broilers. The APEC strains are assigned to a few distinct phylogenetic groups. The purpose of the present study was to detect the virulence genes and phylogenetic groups of E. coli isolates from colibacillosis cases in Japanese quail in 2014 in Kerman, Iran. In the present study, one hundred and two E. coli isolates were obtained from dead Japanese quails with colibacillosis. E. coli isolates were confirmed by standard biochemical and bacteriological methods. DNA of E. coli isolates was extracted by boiling method. The confirmed E. coli isolates were investigated to detect the phylogenetic groups and virulence genes including sfa/focDE, afaIBC, papEF by PCR methods. E. coli isolates were classified into A (62 isolates), B1 (24 isolates), B2 (12 isolates) and D (four isolates) phylogenetic groups. Among examined isolates nine isolates (8.82%) were positive for papE-F, five isolates (4.90%) for afaIB-C and two isolates (1.96%) for sfa/focD-E genes. Based on our findings, E. coli isolates from colibacillosis of Japanese quail could be assigned to various phylogenetic groups (mostly A and D), and they may contain the adhesion genes in a low prevalence.
机译:禽病原性大肠杆菌(APEC)引起的大肠杆菌感染是对全世界禽业的经济威胁。一些毒力基因可能会增强大肠杆菌分离物在肉鸡组织中生长的能力。 APEC菌株被划分为几个不同的系统发育组。本研究的目的是检测2014年在伊朗克尔曼的日本鹌鹑大肠杆菌病病例中分离的大肠杆菌的毒力基因和系统发生群。在本研究中,从死于日本大肠杆菌病的鹌鹑中获得了102个大肠杆菌分离株。大肠杆菌分离物通过标准的生化和细菌学方法确认。通过煮沸法提取大肠杆菌分离物的DNA。对证实的大肠杆菌分离物进行了研究,以通过PCR方法检测系统发生群和毒力基因,包括sfa / focDE,afaIBC,papEF。大肠杆菌分离株分为系统发生群A(62个分离株),B1(24个分离株),B2(12个分离株)和D(四个分离株)。在检查的分离株中,有9株(8.82%)的papE-F阳性,5株(4.90%)的afaIB-C阳性,2株(1.96%)的sfa / focD-E基因阳性。根据我们的发现,日本鹌鹑大肠杆菌病分离株的大肠杆菌分离物可分为多个系统发生组(主要是A和D),并且它们的黏附基因可能患病率较低。

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