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单纯疱疹病毒1型17 + γ34.5缺失突变体1716在重症联合免疫缺陷(SCID)小鼠中无致病性。

The herpes simplex virus type 1 strain 17+ gamma 34.5 deletion mutant 1716 is avirulent in SCID mice.

作者信息

Valyi-Nagy T, Fareed M U, O'Keefe J S, Gesser R M, MacLean A R, Brown S M, Spivack J G, Fraser N W

机构信息

Wistar Institute, Philadelphia, Pennsylvania 19104.

出版信息

J Gen Virol. 1994 Aug;75 ( Pt 8):2059-63. doi: 10.1099/0022-1317-75-8-2059.

Abstract

Laboratory animal models are important tools for the identification of avirulent herpes simplex virus type 1 (HSV-1) strains which have potential for use in humans as vaccine strains or gene therapy vectors. We have studied an HSV-1 17+ variant, 1716, that has a deletion in the gamma 34.5 gene and which replicates poorly in the footpads of mice and is unable to grow in the mouse central nervous system or dorsal root ganglia (DRG) of the peripheral nervous system following peripheral inoculation. However, 1716 is known to be capable of establishing latent infections in the DRG of mice. Here we show that 1716 is avirulent after ocular infection and has low virulence after intracranial inoculation in SCID mice. Since SCID mice are much more sensitive to HSV-1 infection than immunocompetent mice, our results clearly demonstrate the drastically reduced virulence of the variant 1716 and provide additional support for the hypothesis that this variant would be avirulent in humans.

摘要

实验动物模型是鉴定1型单纯疱疹病毒(HSV-1)无毒株的重要工具,这些无毒株有潜力作为疫苗株或基因治疗载体应用于人类。我们研究了一种HSV-1 17+变体,即1716,其γ34.5基因存在缺失,在小鼠足垫中复制能力差,在外周接种后无法在小鼠中枢神经系统或外周神经系统的背根神经节(DRG)中生长。然而,已知1716能够在小鼠的DRG中建立潜伏感染。在此我们表明,1716经眼部感染后无毒,在SCID小鼠中颅内接种后毒力较低。由于SCID小鼠比具有免疫能力的小鼠对HSV-1感染更为敏感,我们的结果清楚地证明了变体1716的毒力大幅降低,并为该变体在人类中无毒的假说提供了额外支持。

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