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抗神经坏死病毒重组多表位疫苗的研制与评价

Development and evaluation of recombinant multi-epitopes vaccine against nervous necrosis virus.

作者信息

Zhang Chen, Zhao Wei-Nan, Liu Xin-Xin, Song Wen-Ye, Peng Hai-Hua, Yang Min, Li Peng-Fei, Wei Jin-Qi, Zhou Yong-Can, Sun Yun

机构信息

School of Marine Biology and Fisheries, Sanya Institute of Breeding and Multiplication, Collaborative Innovation Center of Marine Science and Technology, Hainan University, China.

Key Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, Hainan Medical University, China.

出版信息

Fish Shellfish Immunol. 2025 Jul;162:110332. doi: 10.1016/j.fsi.2025.110332. Epub 2025 Apr 11.

Abstract

Capsid protein (CP) is the antigen of nervous necrosis virus (NNV), a fatal microorganism for almost marine fishes. Antigen epitope is a special chemical group in an antigen molecule that determines the specificity of the antigen, usually consisting of 5-15 amino acid residues. However, the antigen epitope of NNV antigen remains unclear. In this study, using immunoinformatic method, we analyzed the antigen epitope of CP and designed a multi-epitopes vaccine of NNV (PA). Furthermore, we evaluated the immune responses induced by PA vaccine. The results showed that three cytotoxic T lymphocyte epitopes and six B-cell lymphocyte epitopes were predicted, with high antigenicity, non-allergen, and non-toxin. Based on these epitopes, a multi-epitopes vaccine of NNV (PA) was designed and prepared. After immunization, the mRNA expression levels of IL-1β, TNF-α, CD4, CD8, MHC-Ⅰ, and MHC-Ⅱ in PA group were significantly up-regulated. Moreover, it has been proven that PA could significantly activate antigen presenting cells. Importantly, PA could induce similar levels of antibodies secretion and immune protection, compared to CP group. The survival rate reached 77.22 % in PA group. This study provides a cheap and effective strategy for aquatic vaccine design, which will be beneficial in application to development of vaccine in aquaculture industry.

摘要

衣壳蛋白(CP)是神经坏死病毒(NNV)的抗原,NNV对几乎所有海洋鱼类来说都是一种致命微生物。抗原表位是抗原分子中决定抗原特异性的特殊化学基团,通常由5至15个氨基酸残基组成。然而,NNV抗原的抗原表位仍不清楚。在本研究中,我们采用免疫信息学方法分析了CP的抗原表位,并设计了一种NNV多表位疫苗(PA)。此外,我们评估了PA疫苗诱导的免疫反应。结果显示,预测出了三个细胞毒性T淋巴细胞表位和六个B淋巴细胞表位,它们具有高抗原性、无过敏原性且无毒性。基于这些表位,设计并制备了一种NNV多表位疫苗(PA)。免疫后,PA组中IL-1β、TNF-α、CD4、CD8、MHC-Ⅰ和MHC-Ⅱ的mRNA表达水平显著上调。此外,已证明PA能显著激活抗原呈递细胞。重要的是,与CP组相比,PA能诱导相似水平的抗体分泌和免疫保护。PA组的存活率达到了77.22%。本研究为水产疫苗设计提供了一种廉价且有效的策略,这将有利于在水产养殖业中应用疫苗开发。

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