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Escherichia coli cellulitis in broiler chickens: clonal relationships among strains and analysis of virulence-associated factors of isolates from diseased birds.

机译:肉鸡的大肠杆菌蜂窝织炎:品系之间的克隆关系和病禽分离株的毒力相关因子分析。

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摘要

Thirty-nine Escherichia coli isolates from broiler chickens with cellulitis were serotyped and analyzed for clonal relationships by multilocus enzyme electrophoresis. The isolates were further characterized with respect to hemagglutination (HA); serum resistance; antibiotic susceptibility; production of aerobactin, colicin V, and hemolysin; expression of K1 or K5 capsule; sensitivity to cloacin DF13 after treatment with diphenylamine; expression of iron-regulated outer membrane proteins; and virulence in 1-day-old chickens. In addition, the isolates were examined for the presence of DNA sequences related to F1A (fim) and P (pap) fimbriae, aerobactin synthesis (iuc) and transport (iut), hemolysin operon hly, and TraT lipoprotein-induced serum resistance (traT). Only 38.4% of the isolates were typeable with standard O antisera, and of these, serogroups O25 and O78 were the most frequently observed. Multilocus enzyme electrophoresis, based on 20 enzymes, resolved 17 electrophoretic types, forming seven clusters. Isolates from four of these clusters fell into E. coli clone complexes that have been previously reported to be commonly associated with avian colibacillosis. All isolates expressed two to five iron-regulated outer membrane proteins, were resistant to serum and cloacin DF13, and possessed DNA sequences homologous to fim and iuc/iut. Most isolates (72%) were positive for traT, and a majority produced colicin V and aerobactin (92 and 82%, respectively). Assays for the presence of fim and pap DNA sequences, for HA, and for virulence gave variable results but suggest that cellulitis isolates may express F1A and/or other mannose-resistant HA fimbriae different from P and may be virulent in 1-day-old chickens. Our results support the hypothesis that cellulitis in broilers in many cases is caused by E. coli clones identical to other pathogenic avian E. coli strains. Certain clones may be specific to cellulitis, because 25% of the isolates tested belong to clusters not related to known clone complexes.
机译:对来自患有蜂窝炎的肉鸡的39株大肠杆菌进行血清分型,并通过多基因座酶电泳分析其克隆关系。分离物的血凝(HA)进一步表征。血清抵抗力抗生素敏感性产生气杆菌素,大肠菌素V和溶血素;表达K1或K5胶囊;二苯胺处理后对cloacin DF13的敏感性;铁调节的外膜蛋白的表达;和1日龄鸡的毒力。此外,检查了分离株是否存在与F1A(fim)和P(pap)菌毛,气杆菌素合成(iuc)和转运(iut),溶血素操纵子,以及TraT脂蛋白诱导的血清抗性(traT)相关的DNA序列。 )。只有38.4%的分离株可通过标准O抗血清分型,其中O25和O78血清型最常见。基于20种酶的多基因座酶电泳可解析17种电泳类型,形成7个簇。来自这些簇中的四个的分离物落入大肠杆菌克隆复合物中,以前据报道它们通常与禽大肠杆菌病有关。所有分离株均表达2到5个铁调节的外膜蛋白,对血清和cloacin DF13具有抗性,并具有与fim和iuc / iut同源的DNA序列。多数分离株(72%)的traT阳性,大多数产生大肠菌素V和气杆菌素(分别为92和82%)。关于fim和pap DNA序列的存在,HA以及毒力的测定给出了可变的结果,但是表明蜂窝组织炎分离株可能表达F1A和/或其他不同于P的甘露糖耐性HA菌毛,并且在1天大的婴儿中可能具有毒性鸡。我们的结果支持以下假设:肉鸡中的蜂窝组织炎在许多情况下是由与其他致病性禽大肠杆菌菌株相同的大肠杆菌克隆引起的。某些克隆可能对蜂窝织炎具有特异性,因为测试的分离株中有25%属于与已知克隆复合物无关的簇。

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