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首页> 外文期刊>Fish & Shellfish Immunology >Asd-based balanced-lethal system in attenuated Edwardsiella tarda to express a heterologous antigen for a multivalent bacterial vaccine
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Asd-based balanced-lethal system in attenuated Edwardsiella tarda to express a heterologous antigen for a multivalent bacterial vaccine

机译:减毒的爱德华氏菌中基于Asd的平衡致死系统表达多价细菌疫苗的异源抗原

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Edwardsiella tarda is an enteric Gram-negative invasive intracellular pathogen, which causes enteric septicemia in fish. It could be potentially used to develop a recombinant attenuated E. tarda vaccine for the aquaculture industry. Because live vaccine strains can potentially be released into the environment upon vaccination, medical and environmental safety issues must be considered. Deletion of the asdB gene in E tarda resulted in a diaminopimelic acid (DAP)-dependent mutant. The wild type asdB gene was inserted in place of the antibiotic-resistance gene in the plasmid, and the resultant non-antibiotic resistant vector was transformed into the attenuated and DAP-dependent E. tarda vaccine strain (WEDAasdB) to obtain a balanced-lethal system for heterologous antigen expression. The balanced-lethal expression system was further optimized by comparing plasmid replicons with different Shine-Dalgarno sequences and start codons for the asdB gene. Utilizing the optimized balanced-lethal expression system, the protective antigen gene gapA34 from the fish pathogen Aeromonas hydrophila LSA34 was expressed in the attenuated E. tarda to generate the multivalent vaccine candidate WEDAasd B/pUTta4DGap. This vaccine was shown to evoke an effective immune response against both E. tarda and A. hydrophila LSA34 by vaccinating turbot via a simple immersion route. This multivalent E. tarda vector vaccine has great potential for broad applications in aquaculture.
机译:泰氏爱德华氏菌是一种肠道革兰氏阴性侵入性细胞内病原体,可导致鱼类肠道败血症。它可能被潜在地用于开发用于水产养殖业的重组减毒大肠埃希氏菌疫苗。由于活疫苗株可能会在接种疫苗后释放到环境中,因此必须考虑医疗和环境安全问题。在E tarda中删除asdB基因导致了二氨基庚二酸(DAP)依赖性突变体。将野生型asdB基因插​​入质粒中的抗药性基因位置,然后将所得的非抗药性载体转化为减毒且依赖DAP的塔氏大肠杆菌疫苗株(WEDAasdB),以获得平衡致死性异源抗原表达系统。通过比较具有不同Shine-Dalgarno序列的质粒复制子和asdB基因的起始密码子,进一步优化了平衡致死表达系统。利用优化的平衡致死表达系统,将来自鱼病原体嗜水气单胞菌LSA34的保护性抗原基因gapA34在减毒的大肠杆菌中表达,以产生多价疫苗候选物WEDAasd B / pUTta4DGap。通过简单的浸没途径对大菱turbo进行疫苗接种,该疫苗显示出对塔氏大肠杆菌和嗜水曲霉LSA34的有效免疫反应。这种多价大肠杆菌载体疫苗在水产养殖中具有广阔的应用前景。

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