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An approach to a FMD vaccine based on genetic engineered attenuated pseudorabies virus: one experiment using VP1 gene alone generates an antibody responds on FMD and pseudorabies in swine

机译:一种基于基因工程减毒伪狂犬病病毒的口蹄疫疫苗的方法:仅使用VP1基因的一项实验就产生了一种对猪口蹄疫和伪狂犬病有反应的抗体

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摘要

Foot-and-mouth disease (FMD) and pseudorabies (PR) are two important infectious diseases in swine. An attenuated pseudorabies virus (PRV) has been successfully used as a gene delivery vector for the development of live-viral vaccines. In this study, a recombinant PRV-VP1 virus was constructed by fusioning the VP2 gene of FMD virus in frame to the N-terminal sequence of the gG gene of PRV. To test the protective immunity, 15 FMDV sero-negative white swine were divided into three groups and immunized with the recombinant PRV-VP1 virus, commercial FMD vaccine and vector virus (TK-/gG(-)/LacZ(+)), respectively, and challenged intramuscularly with 20 minimal infecting doses (MID) of virulent type 0 FMDV 4 weeks after booster immunization. Swine vaccinated with PRV-VP1 acquired antibodies against both FMDV and PRV, however, anti-FMDV antibodies were much lower than those vaccinated with the commercial FMD vaccine. Our results suggested that the recombinant PRV-VP1 virus, which only expressed FMDV VP1 gene controlled by PRV gG promoter, could not protect swine from the challenge of 20 MID type 0 FMDV, but could delay and reduce the clinical symptoms of FMD.
机译:口蹄疫(FMD)和伪狂犬病(PR)是猪的两种重要传染病。减毒的伪狂犬病病毒(PRV)已成功用作基因传递载体,用于开发活病毒疫苗。在这项研究中,通过将符合框架的FMD病毒的VP2基因与PRV的gG基因的N端序列融合,构建了重组PRV-VP1病毒。为了测试保护性免疫,将15株FMDV血清阴性的白猪分为三组,分别用重组PRV-VP1病毒,商业FMD疫苗和载体病毒(TK- / gG(-)/ LacZ(+))进行免疫。 ,并在加强免疫后4周用20种最小感染剂量(MID)的强毒0型FMDV进行肌内攻击。接种了PRV-VP1疫苗的猪获得了针对FMDV和PRV的抗体,但是抗FMDV抗体的含量远低于使用商业FMD疫苗接种的抗体。我们的结果表明,仅表达由PRV gG启动子控制的FMDV VP1基因的重组PRV-VP1病毒不能保护猪免受20 MID 0型FMDV的攻击,但可以延迟并减轻FMD的临床症状。

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