College of Animal Science and Technology, Northeast Agricultural University, Harbin, 150030, PR China.
College of Animal Science and Technology, Northeast Agricultural University, Harbin, 150030, PR China.
Fish Shellfish Immunol. 2020 May;100:18-26. doi: 10.1016/j.fsi.2020.03.001. Epub 2020 Mar 4.
Infectious pancreatic necrosis virus (IPNV) primarily infects larvae and young salmonid with serious economic losses, which causes haemorrhage and putrescence of hepatopancreas. To develop a more effective oral vaccine against IPNV infection, the aeromonas hydrophila adhesion (AHA1) gene was used as a targeting molecule for intestinal epithelial cells. A genetically engineered Lactobacillus casei (pPG-612-AHA1-CK6-VP2/L. casei 393) was constructed to express the AHA1-CK6-VP2 fusion protein. The expression of interest protein was confirmed by western blotting and the immunogenicity of pPG-612-AHA1-CK6-VP2/L. casei 393 was evaluated. And the results showed that more pPG-612-AHA1-CK6-VP2/L. casei 393 were found in the intestinal mucosal surface of the immunized group. The Lactobacillus-derived AHA1-CK6-VP2 fusion protein could induce the production of serum IgM and skin mucus IgT specific for IPNV with neutralizing activity in rainbow trouts. The levels of IL-1β, IL-8 and TNF-α isolated from the lymphocytes stimulated by AHA1-CK6-EGFP produced were significantly higher than EGFP group. For transcription levels of IL-1β, IL-8, CK6, MHC-II, Mx and TNF-1α in the spleen, the result indicated that the adhesion and target chemokine recruit more immune cells to induce cellular immunity. The level of IPNV in the immunized group of pPG-612-AHA1-CK6-VP2/L. casei 393 was significantly lower than that in the control groups. These data indicated that the adhesion and target chemokine could enhance antigen delivery efficiency, which provides a valuable strategy for the development of IPNV recombination Lactobacillus casei oral vaccine in the future.
传染性胰腺坏死病毒 (IPNV) 主要感染幼虫和幼鲑鱼,造成严重的经济损失,导致肝胰腺出血和腐烂。为了开发更有效的 IPNV 感染口服疫苗,使用气单胞菌黏附素 (AHA1) 基因作为肠上皮细胞的靶向分子。构建了一种遗传工程乳酸乳球菌(pPG-612-AHA1-CK6-VP2/L. casei 393)来表达 AHA1-CK6-VP2 融合蛋白。通过 Western blot 确认目的蛋白的表达,并评估了 pPG-612-AHA1-CK6-VP2/L. casei 393 的免疫原性。结果表明,更多的 pPG-612-AHA1-CK6-VP2/L. casei 393 存在于免疫组的肠黏膜表面。乳酸乳球菌衍生的 AHA1-CK6-VP2 融合蛋白可诱导虹鳟血清 IgM 和皮肤黏液 IgT 产生针对 IPNV 的中和活性。从 AHA1-CK6-EGFP 刺激的淋巴细胞中分离出的 IL-1β、IL-8 和 TNF-α 的水平明显高于 EGFP 组。对于脾中 IL-1β、IL-8、CK6、MHC-II、Mx 和 TNF-1α 的转录水平,结果表明黏附和靶向趋化因子募集更多的免疫细胞以诱导细胞免疫。pPG-612-AHA1-CK6-VP2/L. casei 393 免疫组的 IPNV 水平明显低于对照组。这些数据表明,黏附和靶向趋化因子可以提高抗原递呈效率,为未来开发 IPNV 重组乳酸乳球菌口服疫苗提供了有价值的策略。