Yamazaki S, Notkins A L
J Virol. 1973 Apr;11(4):473-8. doi: 10.1128/JVI.11.4.473-478.1973.
Lactic dehydrogenase virus replicated rapidly in monolayers of primary mouse embryo cells and reached a titer of 10(8) mean infective dose per ml within 18 h after infection. Despite the high virus yield, cytopathology was not observed. Examination of the tissue culture media failed to reveal any evidence of interferon, but the virus was found to be as sensitive to mouse interferon as vesicular stomatitis virus. Incubation of mouse embryo cells with actinomycin D markedly inhibited viral replication, whereas cytosine-beta-d-arabinofuranoside and 5-fluorodeoxyuridine had no effect on replication. These findings indicate that new DNA synthesis is not required but suggest that the intact function of cellular DNA may be required for lactic dehydrogenase virus replication.
乳酸脱氢酶病毒在原代小鼠胚胎细胞单层中迅速复制,感染后18小时内达到每毫升10⁸平均感染剂量的滴度。尽管病毒产量很高,但未观察到细胞病变。对组织培养基的检查未发现任何干扰素的证据,但发现该病毒对小鼠干扰素的敏感性与水疱性口炎病毒相同。用放线菌素D孵育小鼠胚胎细胞可显著抑制病毒复制,而胞嘧啶-β-D-阿拉伯呋喃糖苷和5-氟脱氧尿苷对复制无影响。这些发现表明乳酸脱氢酶病毒复制不需要新的DNA合成,但提示细胞DNA的完整功能可能是其复制所必需的。