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一种基于基因工程减毒伪狂犬病病毒的口蹄疫疫苗研发方法:仅使用VP1基因进行的一项实验可在猪体内引发针对口蹄疫和伪狂犬病的抗体反应。

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.

作者信息

Qian Ping, Li Xiang-Min, Jin Mei-Lin, Peng Gui-Qing, Chen Huan-Chun

机构信息

Laboratory of Animal Virology, College of Veterinary Medical Sciences, Huazhong Agricultural University, Wuhan 430070, PR China.

出版信息

Vaccine. 2004 Jun 2;22(17-18):2129-36. doi: 10.1016/j.vaccine.2003.12.005.

Abstract

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 VP1 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 O 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 O FMDV, but could delay and reduce the clinical symptoms of FMD.

摘要

口蹄疫(FMD)和伪狂犬病(PR)是猪的两种重要传染病。一种减毒伪狂犬病病毒(PRV)已成功用作基因传递载体,用于开发活病毒疫苗。在本研究中,通过将口蹄疫病毒的VP1基因与PRV的gG基因的N端序列框内融合,构建了重组PRV-VP1病毒。为了测试保护性免疫,将15头FMDV血清阴性的白色猪分为三组,分别用重组PRV-VP1病毒、市售FMD疫苗和载体病毒(TK(-)/gG(-)/LacZ(+))进行免疫,并在加强免疫4周后肌肉注射20个最小感染剂量(MID)的强毒O型口蹄疫病毒进行攻毒。用PRV-VP1免疫的猪获得了针对FMDV和PRV的抗体,然而,抗FMDV抗体远低于用市售FMD疫苗免疫的猪。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个MID O型FMDV的攻毒,但可以延迟和减轻FMD的临床症状。

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