Addison C, Rixon F J, Palfreyman J W, O'Hara M, Preston V G
Virology. 1984 Oct 30;138(2):246-59. doi: 10.1016/0042-6822(84)90349-0.
A herpes simplex virus type 1 (HSV-1) mutant, ts1204, which has a temperature-sensitive (ts) mutation located within genome map coordinates 0.318 to 0.324, close to but outside the coding sequences of the glycoprotein gB gene, has been characterised. Although this mutant adsorbed to the cell surface at the nonpermissive temperature (NPT), it failed to penetrate the cell membrane. As a consequence of this defect, high multiplicities of infection of ts1204 blocked subsequent infection of cells by wild-type HSV-1. By contrast, at the NPT, superinfection of cells with HSV-2 was not inhibited by prior infection with ts1204. The penetration defect could be overcome either by brief incubation of mutant virus-infected cells at the permissive temperature, or by treatment of the cells with polyethylene glycol, a compound which promotes fusion of membranes. Upon continued incubation of ts1204-infected cells at the NPT, low numbers of capsids were assembled. Although these capsids all had some internal structure, they did not contain DNA. Another mutant, ts1208, which lies in the same complementation group as ts1204, penetrated cells normally at the NPT, but like ts1204, had a defect in the formation of functional capsids. Evidence presented in this paper suggests that the gene in which the ts1204 and ts1208 lesions map encodes a structural polypeptide.
已对1型单纯疱疹病毒(HSV-1)突变体ts1204进行了特性鉴定,该突变体在基因组图谱坐标0.318至0.324范围内存在温度敏感(ts)突变,该区域靠近糖蛋白gB基因的编码序列但在其外。尽管该突变体在非允许温度(NPT)下能吸附到细胞表面,但未能穿透细胞膜。由于这一缺陷,ts1204的高感染复数会阻止野生型HSV-1随后对细胞的感染。相比之下,在NPT下,用ts1204预先感染细胞并不会抑制HSV-2的超感染。穿透缺陷可以通过在允许温度下短暂孵育突变病毒感染的细胞,或者用促进膜融合的化合物聚乙二醇处理细胞来克服。在NPT下持续孵育ts1204感染的细胞时,会组装出少量衣壳。尽管这些衣壳都有一些内部结构,但它们不含DNA。另一个突变体ts1208与ts1204属于同一互补组,在NPT下能正常穿透细胞,但与ts1204一样,在功能性衣壳形成方面存在缺陷。本文提供的证据表明,ts1204和ts1208损伤所定位的基因编码一种结构多肽。