Ben-Hur T, Asher Y, Tabor E, Darai G, Becker Y
Arch Virol. 1987;96(1-2):117-22. doi: 10.1007/BF01310995.
The phenotype of pathogenicity by direct intracerebral inoculation of herpes simplex virus type 1 (HSV-1) was mapped in the viral genome. This phenotype could be rescued by cotransfection of unit length HSV-1 DNA of an avirulent strain with the BamHI fragment L (0.70-0.738 map units) cloned from a virulent strain. The virulence function was localized in the 2.0 Kb NruI-BamHI fragment in the right-hand side of BamHI-L, the same region that encodes a virus cell-fusion gene (3). Transduction of virulence was linked with the phenotype of a larger plaque size. It is concluded that a neurovirulence function resides in the BamHI-L fragment of the HSV-1 genome, closely linked to the viral gene for cell fusion.
通过直接脑内接种单纯疱疹病毒1型(HSV-1)的致病性表型在病毒基因组中进行了定位。这种表型可以通过将无毒力毒株的单位长度HSV-1 DNA与从有毒力毒株克隆的BamHI片段L(0.70 - 0.738图谱单位)共转染来挽救。毒力功能定位于BamHI-L右侧的2.0 Kb NruI - BamHI片段中,该区域与编码病毒细胞融合基因的区域相同(3)。毒力的转导与更大噬斑大小的表型相关。结论是神经毒力功能存在于HSV-1基因组的BamHI-L片段中,与病毒细胞融合基因紧密相连。