Zhang Mengjie, Chen Xiaoyu, Xue Mingyang, Jiang Nan, Li Yiqun, Fan Yuding, Zhang Peng, Liu Naicheng, Xiao Zidong, Zhang Qinghua, Zhou Yong
National Demonstration Center for Aquatic Animals, Shanghai Ocean University, Shanghai 201306, China.
Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Wuhan 430223, China.
Animals (Basel). 2023 Mar 28;13(7):1183. doi: 10.3390/ani13071183.
Largemouth bass ranavirus (LMBV) infects largemouth bass, leading to significant mortality and economic losses. There are no safe and effective drugs against this disease. Oral vaccines that directly target the intestinal mucosal immune system play an important role in resisting pathogens. Herein, the B subunit of heat-labile enterotoxin (LTB, a mucosal immune adjuvant) and the LMBV main capsid protein (MCP) were expressed using surface display technology. The yeast-prepared oral vaccines were named EBY100-OMCP and EBY100-LTB-OMCP. The candidate vaccines could resist the acidic intestinal environment. After 7 days of continuous oral immunization, indicators of innate and adaptive immunity were measured on days 1, 7, 14, 21, 28, 35, and 42. High activities of immune enzymes (T-SOD, AKP, ACP, and LZM) in serum and intestinal mucus were detected. in the head kidney was significantly upregulated (EBY100-OMCP group: 3.8-fold; BY100-LTB-OMCP group: 4.3-fold). was upregulated in the intestines (EBY100-OMCP group: 5.6-fold; EBY100-LTB-OMCP group: 6.7-fold). Serum neutralizing antibody titers of the two groups reached 1:85. Oral vaccination protected against LMBV infection. The relative percent survival was 52.1% (EBY100-OMCP) and 66.7% (EBY100-LTB-OMCP). Thus, EBY100-OMCP and EBY100-LTB-OMCP are promising and effective candidate vaccines against LMBV infection.
大口黑鲈蛙病毒(LMBV)感染大口黑鲈,导致大量死亡和经济损失。目前尚无针对该疾病的安全有效药物。直接作用于肠道黏膜免疫系统的口服疫苗在抵抗病原体方面发挥着重要作用。在此,利用表面展示技术表达了不耐热肠毒素的B亚基(LTB,一种黏膜免疫佐剂)和LMBV主要衣壳蛋白(MCP)。酵母制备的口服疫苗分别命名为EBY100 - OMCP和EBY100 - LTB - OMCP。候选疫苗能够抵抗肠道酸性环境。连续口服免疫7天后,在第1、7、14、21、28、35和42天测量先天免疫和适应性免疫指标。检测到血清和肠道黏液中免疫酶(T - SOD、AKP、ACP和LZM)活性较高。头肾中的 显著上调(EBY100 - OMCP组:3.8倍;BY100 - LTB - OMCP组:4.3倍)。肠道中的 上调(EBY100 - OMCP组:5.6倍;EBY100 - LTB - OMCP组:6.7倍)。两组血清中和抗体效价均达到1:85。口服疫苗可预防LMBV感染。相对存活率分别为52.1%(EBY100 - OMCP)和66.7%(EBY100 - LTB - OMCP)。因此,EBY100 - OMCP和EBY100 - LTB - OMCP是有前景的、有效的抗LMBV感染候选疫苗。