Qian Ping, Li Xiang-Min, Jin Mei-Lin, Peng Gui-Qing, Chen Huan-Chun
Laboratory of Animal Virology, College of Veterinary Medical Sciences, Huazhong Agricultural University, Wuhan 430070, PR China.
Vaccine. 2004 Jun 2;22(17-18):2129-36. doi: 10.1016/j.vaccine.2003.12.005.
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.
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。