Halliburton I W, Timbury M C
J Gen Virol. 1976 Feb;30(2):207-21. doi: 10.1099/0022-1317-30-2-207.
Three new complementation groups of type 2 herpes simplex virus are described bringing the total number of complementation groups characterized to 13. Of the three new groups, ts 11 fails to make virus DNA at non-permissive temperature (38 degrees C) whereas ts 12 and ts 13 synthesize only very small amounts of virus or cellular DNA at 38 degrees C. ts 11, like ts 9 (Halliburton & Timbury, 1973) fails to switch off host cell DNA synthesis at 38 degrees C. That this is a failure to switch off cell DNA rather than a stimulation of cell DNA synthesis was confirmed in experiments using resting cells. Both the inability to make virus DNA and the inability to switch off cell DNA are reversed in temperature shift-down experiments with cells infected with ts 9 or ts 11. In temperature shift-up experiments, cellular DNA synthesis is inhibited after the shift but virus DNA is only made in very small amounts, probably due to the continuing functioning of a protein made at permissive temperature (31 degrees C) before the shift but which cannot be made at 38 degrees C. The shift-down experiments and the fact that ts 9 and ts 11 complement one another, suggest that the switch-off of host cell DNA synthesis may involve more than one virus specified function. U.v. irradiated virus fails to switch off host cell DNA synthesis.
本文描述了2型单纯疱疹病毒的三个新互补群,使已鉴定的互补群总数达到13个。在这三个新群中,ts11在非允许温度(38℃)下无法产生病毒DNA,而ts12和ts13在38℃时仅合成极少量的病毒或细胞DNA。ts11与ts9(Halliburton和Timbury,1973)一样,在38℃时无法关闭宿主细胞DNA合成。在使用静止细胞的实验中证实,这是无法关闭细胞DNA,而不是刺激细胞DNA合成。对于感染ts9或ts11的细胞,在温度下降实验中,无法产生病毒DNA以及无法关闭细胞DNA的情况都会逆转。在温度上升实验中,温度变化后细胞DNA合成受到抑制,但病毒DNA仅以极少量产生,这可能是由于在允许温度(31℃)下在温度变化前产生的一种蛋白质持续发挥作用,但在38℃时无法产生。温度下降实验以及ts9和ts11相互互补的事实表明,宿主细胞DNA合成的关闭可能涉及不止一种病毒特定功能。紫外线照射的病毒无法关闭宿主细胞DNA合成。