Oral Vaccination of Largemouth Bass (Micropterus salmoides) against Largemouth Bass Ranavirus (LMBV) Using Yeast Surface Display Technology

被引:24
作者
Zhang, Mengjie [1 ,2 ,3 ]
Chen, Xiaoyu [4 ]
Xue, Mingyang [2 ]
Jiang, Nan [2 ]
Li, Yiqun [2 ]
Fan, Yuding [2 ]
Zhang, Peng [1 ,2 ,3 ]
Liu, Naicheng [1 ,2 ,3 ]
Xiao, Zidong [2 ]
Zhang, Qinghua [1 ,3 ]
Zhou, Yong [2 ]
机构
[1] Shanghai Ocean Univ, Natl Demonstrat Ctr Aquat Anim, Shanghai 201306, Peoples R China
[2] Chinese Acad Fishery Sci, Yangtze River Fisheries Res Inst, Wuhan 430223, Peoples R China
[3] Shanghai Ocean Univ, Key Lab Explorat & Utilizat Aquat Genet Resources, Minist Educ, Shanghai 201306, Peoples R China
[4] Hefei Customs, Anhui Int Travel Hlth Care Ctr, Hefei 230061, Peoples R China
来源
ANIMALS | 2023年 / 13卷 / 07期
基金
中国国家自然科学基金;
关键词
largemouth bass ranavirus; oral vaccine; Saccharomyces cerevisiae; yeast display technology; mucosal immunization; MAJOR CAPSID PROTEIN; CHINESE GIANT SALAMANDER; HEAT-LABILE ENTEROTOXIN; MUCOSAL IMMUNE-SYSTEM; ESCHERICHIA-COLI; DNA VACCINE; MOLECULAR CHARACTERIZATION; INTESTINAL MORPHOLOGY; PROTECTIVE IMMUNITY; VIRUS;
D O I
10.3390/ani13071183
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
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 Escherichia coli heat-labile enterotoxin (LTB, a mucosal immune adjuvant) and the LMBV main capsid protein (MCP) were expressed using Saccharomyces cerevisiae 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. IgM in the head kidney was significantly upregulated (EBY100-OMCP group: 3.8-fold; BY100-LTB-OMCP group: 4.3-fold). IgT 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.
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页数:18
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