Russell J, Preston C M
J Gen Virol. 1986 Feb;67 ( Pt 2):397-403. doi: 10.1099/0022-1317-67-2-397.
An in vitro latency system for herpes simplex virus type 2 (HSV-2) in cultured cells has been developed. Virus replication was suppressed by infection of human foetal lung cells at the supraoptimal temperature of 42 degrees C, and, following transfer of such cell cultures to the normal growth temperature of 37 degrees C, infectious virus was generally undetectable for at least 6 days. HSV-2 was reactivated by intertypic superinfection at 38.5 degrees C with temperature-sensitive mutants of HSV-1, or with human cytomegalovirus, but not by superinfection with adenovirus types 2 or 5. The HSV-1 mutant tsKsyn, which produces only immediate early polypeptides at 38.5 degrees C, was as effective as the late mutant tsIsyn, but tsK which had been irradiated with u.v. light to prevent gene expression did not reactivate HSV-2. The efficiency of reactivation was very high, since 15 to 34% of the theoretical input of infectious HSV-2 particles could be retrieved by superinfection with 0.3 p.f.u. of tsKsyn per cell. Reactivation of latent virus was not induced by cell subculture or by other treatments which alter cell metabolism. The system described here may be important for studies on the molecular basis of HSV latency.
已开发出一种用于在培养细胞中研究单纯疱疹病毒2型(HSV - 2)体外潜伏系统。通过在42℃的超适温度下感染人胎儿肺细胞来抑制病毒复制,并且,将此类细胞培养物转移至37℃的正常生长温度后,通常至少6天检测不到感染性病毒。HSV - 2可通过在38.5℃下用HSV - 1的温度敏感突变体或人巨细胞病毒进行异型超感染而重新激活,但用2型或5型腺病毒进行超感染则不能激活。在38.5℃仅产生立即早期多肽的HSV - 1突变体tsKsyn与晚期突变体tsIsyn一样有效,但经紫外线照射以阻止基因表达的tsK不能重新激活HSV - 2。重新激活的效率非常高,因为通过每细胞用0.3个噬斑形成单位(p.f.u.)的tsKsyn进行超感染,可回收15%至34%的感染性HSV - 2颗粒理论输入量。细胞传代培养或其他改变细胞代谢的处理不会诱导潜伏病毒的重新激活。此处描述的系统对于研究HSV潜伏的分子基础可能很重要。