Generation and immunogenicity analysis of recombinant classical swine fever virus glycoprotein E2 and E-rns expressed in baculovirus expression system
文献类型: 外文期刊
作者: Wei, Qiang 1 ; Bai, Yilin 1 ; Song, Yapeng 1 ; Liu, Yunchao 1 ; Yu, Wei 1 ; Sun, Yaning 1 ; Wang, Li 1 ; Deng, Ruiguang 1 ;
作者机构: 1.Henan Acad Agr Sci, Henan Prov Key Lab Anim Immunol, Zhengzhou 450002, Peoples R China
2.Northwest A&F Univ, Coll Vet Med, Yangling 712100, Shaanxi, Peoples R China
3.Henan Agr Univ, Coll Anim Sci & Vet Med, Zhengzhou 450002, Henan, Peoples R China
4.Henan Baiao Biol Project Co Ltd, Zhengzhou 450002, Peoples R China
5.Yangzhou Univ, Coll Vet Med, Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou 225009, Jiangsu, Peoples R China
关键词: Classical swine fever virus; Immunogenicity; E2; E-rns
期刊名称:VIROLOGY JOURNAL ( 影响因子:4.099; 五年影响因子:3.719 )
ISSN:
年卷期: 2021 年 18 卷 1 期
页码:
收录情况: SCI
摘要: Classical swine fever (CSF) caused by the classical swine fever virus (CSFV) is a highly contagious swine disease resulting in large economical losses worldwide. The viral envelope glycoprotein E2 and E-rns are major targets for eliciting antibodies against CSFV in infected animals. In this report, the glycoprotein E2 and E-rns were expressed using the baculovirus system and their protective immunity in rabbits were tested. Twenty CSFV seronegative rabbits were randomly divided into five groups. Each rabbit was intramuscularly immunized with CSFV-E2, CSFV-E-rns, or their combination (CSFV-E2 + E-rns). Besides, a commercial CSFV vaccine (C-strain) and PBS were used as positive or negative controls, respectively. Four weeks after the second immunization, all the rabbits were challenged with 100 RID50 of CSFV C-strain. High levels of CSFV E2-specific antibody, neutralizing antibody and cellular immune responses to CSFV were elicited in the rabbits inoculated with C-strain, CSFV-E2, and CSFV-E2 + E-rns. And the rabbits inoculated with the three vaccines received complete protection against CSFV C-strain. However, no neutralizing antibody was detected in the E-rns vaccinated rabbits and the rabbits exhibited fever typical of CSFV, suggesting the E-rns alone is not able to induce a protective immune response. Taken together, while the E-rns could not confer protection against CSFV, E2 and E2 + E-rns could not only elicit humoral and cell-mediated immune responses but also confer complete protection against CSFV C-strain in rabbits.
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