Sohn Min-Young, Jeong Ji-Min, Kang Gyoungsik, Woo Won-Sik, Kim Kyung-Ho, Son Ha-Jeong, Joo Min-Soo, Park Chan-Il
Department of Marine Biology & Aquaculture, College of Marine Science, Gyeongsang National University, 455, Tongyeong, 650-160, Republic of Korea.
Aquatic Disease Control Division, National Fishery Products Quality Management Service (NFQS), 337, Haeyang-ro, Yeongdo-gu, Busan, Republic of Korea, 49111.
Dev Comp Immunol. 2025 Jan;162:105262. doi: 10.1016/j.dci.2024.105262. Epub 2024 Sep 11.
Aquaculture is notably vulnerable to diseases, with Edwardsiella tarda causing significant mortality across various commercially important fish species in both freshwater and marine environments. In the aquaculture industry, sustainable disease control hinges on the effective development of vaccines. Oral vaccines present an appealing approach to immunization in fish due to their ease of antigen administration, reduced stress compared to non-oral delivery methods, and their potential applicability to both small and large finfish species. In mammals, the exposure of mucosal surfaces to antigens results in the secretion of antigen-specific IgA at these locations. Mammals have a common mucosal immune system, in which stimulation of one epithelium can also give rise to specific IgA or IgM responses in other mucosal organs. Mucosal immunoglobulins are particularly important in developing vaccines that provide mucosal immunity. However, it remains unclear whether fish share a common mucosal system. Moreover, neither Peyer's patches nor intestinal lymph nodes were identified. Nevertheless, oral vaccination remains an attractive method for inducing immunity. We investigated whether the activation of the mucosal immune response was induced by direct injection of the antigen. After oral antigen administration, antigen-specific antibody titers increased in the experimental group (E. tarda FKC vaccine). In the challenge experiment, the cumulative survival rate was 72% (E. tarda). This suggests that oral administration of antigens can activate intestinal mucosal immunity in flounders. Additionally, these results help understand the intestinal mucosal immune system of teleost fish. In the future, research on the signaling mechanisms of these genes is expected to provide helpful information for developing vaccine adjuvants.
水产养殖极易受到疾病影响,迟缓爱德华氏菌会在淡水和海洋环境中的多种具有重要商业价值的鱼类中造成大量死亡。在水产养殖业中,可持续的疾病控制取决于疫苗的有效研发。口服疫苗由于抗原给药方便、与非口服给药方法相比应激较小以及对小型和大型硬骨鱼类均有潜在适用性,因而成为鱼类免疫接种的一种有吸引力的方法。在哺乳动物中,黏膜表面暴露于抗原会导致这些部位分泌抗原特异性IgA。哺乳动物有一个共同的黏膜免疫系统,其中一个上皮受到刺激也会在其他黏膜器官引发特异性IgA或IgM反应。黏膜免疫球蛋白在开发提供黏膜免疫的疫苗方面尤为重要。然而,鱼类是否共享一个共同的黏膜系统仍不清楚。此外,未发现派伊尔氏结或肠道淋巴结。尽管如此,口服疫苗接种仍然是一种有吸引力的诱导免疫方法。我们研究了抗原直接注射是否能诱导黏膜免疫反应的激活。口服抗原给药后,实验组(迟缓爱德华氏菌FKC疫苗)的抗原特异性抗体滴度升高。在攻毒实验中(迟缓爱德华氏菌)累计存活率为72%。这表明口服抗原可激活牙鲆的肠道黏膜免疫。此外,这些结果有助于了解硬骨鱼类的肠道黏膜免疫系统。未来,对这些基因信号传导机制的研究有望为开发疫苗佐剂提供有用信息。