Klauck S M, Hampl W, Kleinschmidt A K
Department of Virology, University of Ulm, Federal Republic of Germany.
Arch Virol. 1995;140(7):1195-213. doi: 10.1007/BF01322746.
We studied possible genomic changes occurring in herpes simplex virus type 1 (HSV-1) during long-term cell culture which served as a model system for persistence and latency studies as introduced earlier. Sixteen HSV-1 reisolates were isolated from persistently productive HSV-1 (strains F and AK)-infected Burkitt lymphoma cell lines Raji and BJAB at four different times. They were roughly characterized in plaque morphology, plaque size, and infectivity. The viral reisolate DNAs revealed deletions and insertions of up to 1,150 base pairs in fragments BamHI-B, -E, -F, -J, -V, -X, and in the L-terminal and junction fragments S and K. Results were confirmed by additional restriction enzyme analyses and DNA sequencing of selected genomic regions between map units 0.642-0.650, 0.763-0.778 and 0.887-0.934. There was a progressive increase in genomic variability over a three-year period. However, changes in DNA fragment size occurred at different rates, with some reisolates showing stability over several months. The selective pressure for HSV-1 (F and AK) genomic changes was stronger in Raji than in BJAB cells, and stronger for F than for AK strain.
我们研究了单纯疱疹病毒1型(HSV-1)在长期细胞培养过程中可能发生的基因组变化,如前文所述,该长期细胞培养作为持续性和潜伏性研究的模型系统。在四个不同时间点,从持续产生HSV-1(F株和AK株)感染的伯基特淋巴瘤细胞系Raji和BJAB中分离出16株HSV-1重分离株。对它们的噬斑形态、噬斑大小和感染性进行了大致表征。病毒重分离株的DNA显示,在BamHI-B、-E、-F、-J、-V、-X片段以及L末端和连接片段S和K中存在高达1150个碱基对的缺失和插入。通过额外的限制性内切酶分析以及对图谱单位0.642 - 0.650、0.763 - 0.778和0.887 - 0.934之间选定基因组区域的DNA测序,证实了结果。在三年时间里,基因组变异性逐渐增加。然而,DNA片段大小的变化速率不同,一些重分离株在几个月内表现出稳定性。HSV-1(F株和AK株)基因组变化的选择压力在Raji细胞中比在BJAB细胞中更强,且对F株比对AK株更强。