Center for Proteomics and Metabolomics, State Key Laboratory of Bio-Control, Guangdong Province Key Laboratory for Pharmaceutical Functional Genes, School of Life Sciences, Sun Yat-sen University, University City, Guangzhou, 510006, PR China.
Center for Proteomics and Metabolomics, State Key Laboratory of Bio-Control, Guangdong Province Key Laboratory for Pharmaceutical Functional Genes, School of Life Sciences, Sun Yat-sen University, University City, Guangzhou, 510006, PR China; Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266071, PR China.
Fish Shellfish Immunol. 2018 Apr;75:308-315. doi: 10.1016/j.fsi.2018.02.022. Epub 2018 Feb 10.
Polyvalent vaccines against more than one species of pathogens are especially important due to the complex ecosystem in aquaculture. We have previously shown that the development of polyvalent vaccines by shuffling six ompA genes from different bacteria with V. parahaemolyticus VP0764 primers. Here, we used the same 6 genes, V. alginolyticus VA0764 and VA1186, V. parahaemolyticus VP0764 and VP1186, E. tarda ompA and E. coli ompA, but with E. tarda ompA primers to develop new polyvalent vaccines. By this approach, we identified 7 potential polyvalent vaccines that were effective against both V. alginolyticus and E. tarda infections. Furthermore, the innate immunity triggered by the vaccines were also explored in three groups, no protection (group I), protection against V. alginolyticus (group II), and protection against both V. alginolyticus and E. tarda (group III). The transcription of IL-1β, IL-6, IL-8, C3b and NF-kB were significantly increased in group II and group III but not group I, where the expression level of group III was higher than group II. In addition, differential activities of succinate dehydrogenase were detected among the three groups. These results indicate the expansion of polyvalent vaccine reservoir with the same shuffling genes but different primers, and promote the understanding of the mechanisms of polyvalent vaccines based on vaccine-induced innate immunity.
多价疫苗针对多种病原体特别重要,因为水产养殖中的生态系统非常复杂。我们之前已经表明,通过用副溶血弧菌 VP0764 引物对来自不同细菌的 6 个 ompA 基因进行改组,可以开发多价疫苗。在这里,我们使用相同的 6 个基因,即鳗弧菌 VA0764 和 VA1186、副溶血弧菌 VP0764 和 VP1186、迟缓爱德华氏菌 ompA 和大肠杆菌 ompA,但使用迟缓爱德华氏菌 ompA 引物来开发新的多价疫苗。通过这种方法,我们鉴定了 7 种潜在的多价疫苗,它们对鳗弧菌和迟缓爱德华氏菌感染均有效。此外,还在三组中探索了疫苗引发的固有免疫,分别为无保护(I 组)、对鳗弧菌的保护(II 组)和对鳗弧菌和迟缓爱德华氏菌的双重保护(III 组)。在 II 组和 III 组中,IL-1β、IL-6、IL-8、C3b 和 NF-kB 的转录显著增加,但在 I 组中没有增加,其中 III 组的表达水平高于 II 组。此外,还检测到三组间琥珀酸脱氢酶的活性存在差异。这些结果表明,通过使用相同的改组基因但不同的引物扩展了多价疫苗库,并促进了对基于疫苗诱导固有免疫的多价疫苗机制的理解。