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Functional Genomics Approach to the Identification of Virulence Genes Involved in Edwardsiella tarda Pathogenesis

机译:功能基因组学方法鉴定涉及爱德华氏菌致病性的致病基因

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Edwardsiella tarda is an important cause of hemorrhagic septicemia in fish and also of gastro- and extraintestinal infections in humans. Here, we report the identification of 14 virulence genes of pathogenic E. tarda that are essential for disseminated infection, via a genome-wide analysis. We screened 490 alkaline phosphatase fusion mutants from a library of 450,000 TnphoA transconjugants derived from strain PPD130/91, using fish as an infection model. Compared to the wild type, 15 mutants showed significant decreases in virulence. Six mutants had insertions in the known virulence-related genes, namely, fimA, gadB, katB, pstS, pstC, and ssrB. Some mutants corresponded to known genes (astA, isor, and ompS2) that had not been previously shown to be involved in pathogenesis, and three had insertions in two novel genes. In vivo infection kinetics experiments confirmed the inability of these attenuated mutants to proliferate and cause fatal infection in fish. Screening for the presence of the above-described virulence genes in six virulent and seven avirulent strains of E. tarda indicated that seven of the genes were specific to pathogenic E. tarda. The genes identified here may be used to develop vaccines and diagnostic kits as well as for further studying the pathogenesis of E. tarda and other pathogenic bacteria.
机译:埃德华氏菌是鱼类出血性败血病的重要原因,也是人类胃肠道和肠道外感染的重要原因。在这里,我们报告的致病性 E 14毒力基因的鉴定。通过全基因组分析,对传播感染至关重要的tarda 。我们使用鱼作为感染模型,从来源于菌株PPD130 / 91的450,000个Tn phoA 转导结合体库中筛选了490个碱性磷酸酶融合突变体。与野生型相比,有15个突变体的毒力显着降低。有六个突变体插入了已知的与毒力相关的基因,分别是 fimA gadB katB pstS pstC ssrB 。一些突变体对应于已知基因( astA isor ompS2 ),这些基因先前未显示与发病相关,而三个突变体插入两个新基因。体内感染动力学实验证实了这些减毒突变体无法繁殖并在鱼类中造成致命感染。在6种强毒和7种无毒Em菌株中筛选上述毒力基因的存在。 tarda 指出其中七个基因对致病性 E具有特异性。 tarda 。本文鉴定的基因可用于开发疫苗和诊断试剂盒,以及用于进一步研究 E的发病机理。 tarda 和其他致病菌。

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