Ono E, Tasaki T, Kobayashi T, Taharaguchi S, Nikami H, Miyoshi I, Kasai N, Arikawa J, Kida H, Shimizu Y
Institute of Immunological Science, Hokkaido University, Sapporo, 060-0815, Japan.
Virology. 1999 Sep 15;262(1):72-8. doi: 10.1006/viro.1999.9899.
A chimeric gene encoding a fusion protein consisting of the DNA-binding domain of the immediate-early (IE) protein of pseudorabies virus (PRV) and a tail-truncated VP16 of herpes simplex virus 1, lacking the transcription activation domain, has been shown to repress transcription of the PRV IE gene, resulting in the inhibition of PRV growth in vitro. To assess the antiviral potential of the fusion protein in vivo, transgenic mice containing the chimeric gene under the control of the virus- and interferon-inducible Mx 1 promoter were generated. A transgenic mouse line showed marked resistance to PRV infection when the mice were challenged intranasally with PRV. Inhibition of PRV replication was also observed in monolayers of embryonic cells prepared from the transgenic mice. In the cells infected with PRV, transcription of the PRV IE gene was repressed. The present results indicate that the chimeric gene is able to exert a significant antiviral effect against PRV infection in vivo.
一种嵌合基因编码一种融合蛋白,该融合蛋白由伪狂犬病病毒(PRV)即刻早期(IE)蛋白的DNA结合结构域和单纯疱疹病毒1尾部截短的VP16组成,缺失转录激活结构域,已证明其可抑制PRV IE基因的转录,从而在体外抑制PRV生长。为了评估该融合蛋白在体内的抗病毒潜力,构建了在病毒和干扰素诱导型Mx 1启动子控制下含有嵌合基因的转基因小鼠。当用PRV经鼻攻击小鼠时,一个转基因小鼠品系对PRV感染表现出显著抗性。在从转基因小鼠制备的胚胎细胞单层中也观察到PRV复制受到抑制。在感染PRV的细胞中,PRV IE基因的转录受到抑制。目前的结果表明,该嵌合基因能够对体内PRV感染发挥显著的抗病毒作用。