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Genotyping of Campylobacter jejuni strains from Danish broiler chickens by restriction fragment length polymorphism of the LPS gene cluster

机译:LPS基因簇的限制性片段长度多态性对丹麦肉鸡空肠弯曲菌的基因分型。

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Aims: To apply and evaluate LG (LPS genes) genotyping, which is a genotyping method based on a cluster of genes involved in the synthesis of surface lipopolysaccharides (LPS) in Campylobacter species, for typing of Campylobacter jejuni isolates obtained from Danish broiler chickens. Furthermore, the LG genotyping method was used to study the genetic stability of four C. jejuni strains after gastrointestinal passage through experimentally infected chickens.Methods and Results: In the present study, the LG genotyping method was modified with respect to the restriction enzymes used. To validate the method, 63 Penner serotype reference strains and 107 C. jejuni chicken isolates, representing the most common Penner serotypes of C. jejuni in Danish poultry, were selected for typing. The method was successfully used for typing all isolates and the LG genotype profiles were reproducible. There were no changes in the LG genotype of the C. jejuni strains obtained after experimental passage through chickens.Concusions: All C. jejuni strains obtained from broiler chickens were typeable by the LG genotyping method. Application of the RsaI restriction enzyme improved the method in terms of ease and consistency of analyses and increase of discriminatory power.Significance and Impact of the Study: The LG genotyping method is a valuable tool for typing C. jejuni isolates obtained from poultry. However, the association between Penner serotyping based on passive haemagglutination of heat-stable antigens and LG genotyping was low when applied to poultry isolates. This is in contrast to previous studies on isolates of human origin that reported a high correlation between results obtained by the two typing methods.
机译:目的:应用和评估LG(LPS基因)基因分型方法,这是一种基于弯曲杆菌属中表面脂多糖(LPS)合成相关基因簇的基因分型方法,用于对从丹麦肉鸡获得的空肠弯曲杆菌分离株进行分型。此外,LG基因分型方法被用于研究4种空肠弯曲杆菌菌株在胃肠道通过实验感染的鸡后的遗传稳定性。方法和结果:在本研究中,针对所使用的限制酶对LG基因分型方法进行了改进。为了验证该方法,选择了63种Penner血清型参考菌株和107个空肠弯曲杆菌鸡分离株,它们代表了丹麦家禽中空肠弯曲杆菌的最常见Penner血清型。该方法已成功用于所有分离株的分型,并且LG基因型谱具有可重复性。实验通过鸡后获得的空肠弯曲杆菌菌株的LG基因型没有变化。结论:所有从肉鸡获得的空肠弯曲杆菌菌株均可以通过LG基因分型方法进行分型。 RsaI限制性内切酶的应用从分析的简便性和一致性以及鉴别力的提高方面改进了该方法。研究的意义和影响:LG基因分型方法是用于鉴定从家禽获得的空肠弯曲杆菌分离株的有价值的工具。然而,当应用于家禽分离株时,基于热稳定抗原的被动血凝的彭纳血清分型与LG基因分型之间的关联性很低。这与先前关于人类分离株的研究相反,后者报道了两种分型方法获得的结果之间的高度相关性。

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