Key Laboratory of Virology and Biosafety, Chinese Academy of Sciences, Wuhan 430071, China.
University of Chinese Academy of Sciences, Beijing 101499, China.
Viruses. 2023 Nov 14;15(11):2256. doi: 10.3390/v15112256.
Human herpes simplex virus (HSV), a double-stranded DNA virus belonging to the family and alpha herpesvirus subfamily, is one of the most epidemic pathogens in the population. Cell-to-cell spread is a special intercellular transmission mechanism of HSV that indicates the virulence of this virus. Through numerous studies on mutant HSV strains, many viral and host proteins involved in this process have been identified; however, the mechanisms remain poorly understood. Here, we evaluated the effect of the membrane protein genes and on cell-to-cell spread in vitro between two HSV-1 (HB94 and HN19) strains using a plaque assay, syncytium formation assay, and the CRISPR/Cas9 technique. knockout resulted in the inhibition of viral cell-to-cell spread; additionally, glycoprotein I () of the HB94 strain was found to promote cell-to-cell spread compared to that of the HN19 strain. knockout did not affect plaque size and syncytium formation; however, the gene product of from the HN19 strain inhibited plaque formation and membrane infusion. This study presents preliminary evidence of the functions of and in the cell-to-cell spread of HSV-1, which will provide important clues to reveal the mechanisms of cell-to-cell spread, and contributes to the clinical drugs development.
人类单纯疱疹病毒(HSV)是一种双链 DNA 病毒,属于疱疹病毒科和α疱疹病毒亚科,是人群中最流行的病原体之一。细胞间传播是 HSV 的一种特殊细胞间传播机制,表明该病毒的毒力。通过对突变 HSV 株的大量研究,已经鉴定出许多参与该过程的病毒和宿主蛋白;然而,其机制仍知之甚少。在这里,我们使用噬斑试验、合胞体形成试验和 CRISPR/Cas9 技术评估了膜蛋白基因和在两种 HSV-1(HB94 和 HN19)株之间体外细胞间传播中的作用。基因敲除导致病毒细胞间传播受到抑制;此外,与 HN19 株相比,HB94 株的糖蛋白 I()被发现促进细胞间传播。基因敲除不影响噬斑大小和合胞体形成;然而,HN19 株的基因产物抑制了斑块形成和膜浸润。本研究初步证明了和在 HSV-1 细胞间传播中的作用,这将为揭示细胞间传播机制提供重要线索,并有助于临床药物的开发。