首页> 外文期刊>Journal of applied microbiology >Genetic relationships of Edwardsiella strains isolated in China aquaculture revealed by rep-PCR genomic fingerprinting and investigation of Edwardsiella virulence genes.
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Genetic relationships of Edwardsiella strains isolated in China aquaculture revealed by rep-PCR genomic fingerprinting and investigation of Edwardsiella virulence genes.

机译:通过rep-PCR基因组指纹图谱和爱德华氏菌毒力基因的研究揭示了中国水产养殖中爱德华氏菌菌株的遗传关系。

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Aims: The aim of this study was to classify Edwardsiella strains isolated from China aquaculture based on biochemical and molecular methods. Methods and Results: In this study, biochemical characterization of 19 Edwardsiella tarda isolates and two Edwardsiella ictaluri isolates was performed with API 20E system. Other pathogenicity-related phenotypes such as haemagglutination, haemolytic activities and lethality to fish were also examined in these strains. As it was difficult to categorize the subgroups of Edw. tarda according to their origins or phenotypic properties, three PCR-based methods, i.e. PCR amplification of virulence genes, Enterobacterial repetitive intergenic consensus-PCR and BOX-PCR, were carried out to further resolve the relatedness of the Edw. tarda isolates. As a result, all Edw. tarda isolates could be generally grouped into pathogenic and nonpathogenic branches before being classified into strain-specific or origin-specific clades. Conclusions: Biochemical characterization was sensitive for interspecific typing, while PCR-based approaches permitted a more accurate discrimination for intraspecific typing resulting in pathogenic and nonpathogenic clusters and further more delicate clades for Edwardsiella. Significance and Impact of the Study: PCR-based genomic fingerprinting to study the relatedness and trace the pathogenicity of the Edwardsiella strains will be helpful in investigating the virulence factors of Edwardsiella and in the development of vaccines and diagnostics for edwardsiellosis.
机译:目的:本研究的目的是基于生化和分子方法对从中国水产养殖中分离的爱德华氏菌菌株进行分类。方法和结果:在本研究中,使用API​​ 20E系统对19株泰德爱德华氏菌和2株埃德华氏菌进行了生化鉴定。在这些菌株中还检查了其他与致病性有关的表型,例如血凝,溶血活性和对鱼类的致死性。由于很难对 Edw的子组进行分类。根据tarda 的起源或表型特性,进行了三种基于PCR的方法,即毒力基因的PCR扩增,肠杆菌重复性基因间共有PCR和BOX-PCR,以进一步解决埃德tarda 分离株。结果,所有 Edw。 tarda分离株通常可以分为致病性分支和非致病性分支,然后再分为特定菌株或特定起源进化枝。结论:生化特性对种间分型敏感,而基于PCR的方法可以对种内分型进行更准确的区分,从而导致致病性和非致病性簇,以及爱德华氏菌的更精细分支。研究的意义和影响:基于PCR的基因组指纹图谱研究埃德华氏菌菌株的相关性并追踪其致病性,将有助于调查埃德华氏菌的毒力因子和埃德氏病疫苗和诊断方法的开发。

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