Immunogenicity and protective efficacy of recombinant proteins consisting of multiple epitopes of foot-and-mouth disease virus fused with flagellin
文献类型: 外文期刊
第一作者: Cui, Baofeng
作者: Cui, Baofeng;Liu, Xinsheng;Zhou, Peng;Fang, Yuzhen;Zhao, Donghong;Zhang, Yongguang;Wang, Yonglu;Cui, Baofeng;Liu, Xinsheng;Zhou, Peng;Fang, Yuzhen;Zhao, Donghong;Zhang, Yongguang;Wang, Yonglu;Cui, Baofeng
作者机构:
关键词: FMDV; Epitope; Flagellin; Recombinant fusion; Vaccine
期刊名称:APPLIED MICROBIOLOGY AND BIOTECHNOLOGY ( 影响因子:4.813; 五年影响因子:4.697 )
ISSN: 0175-7598
年卷期: 2019 年 103 卷 8 期
页码:
收录情况: SCI
摘要:
Many recent studies have shown that flagellin fused to heterologous antigens can induce significantly enhanced humoral and cellular immune responses through its adjuvant activity. Therefore, in this study, two key B cell epitopes and a truncated VP1 (VP1) protein from foot-and-mouth disease virus (FMDV) were expressed as flagellin fusion proteins in different patterns. Specifically, VP1 and two duplicates of two key B cell epitopes (2xB1B2) were fused separately to the C-terminus of flagellin with a universal exogenous T cell epitope to construct FT (Flagellin-Truncated VP1) and FME (Flagellin-Multiple Epitopes). In addition, the D3 domain of flagellin was replaced by VP1 in FME, yielding FTME (Flagellin-Truncated VP1-Multiple Epitopes). The immunogenicity and protective efficacy of the three fusion proteins as novel FMDV vaccine candidates were evaluated. The results showed that FT, FME, and FTME elicited significant FMDV-specific IgG responses at 10g/dose compared with the mock group (P<0.05), with FTME producing the highest response. No significant differences in the antibody response to FTME were observed between different immunization routes or among adjuvants (ISA-206, poly(I
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