Weck P K, Carroll A R, Shattuck D M, Wagner R R
J Virol. 1979 Jun;30(3):746-53. doi: 10.1128/JVI.30.3.746-753.1979.
UV irradiation of infectious vesicular stomatitis virus was employed to study the relationship between the expression of certain viral gene functions and viral inhibition of RNA synthesis in mouse myeloma (MPC-11) cells. Viral infectivity, protein synthesis, and viral mRNA synthesis were all highly susceptible to inactivation by UV radiation; however, low levels of viral transcriptase activity were detected in vitro in virus preparations subjected to large doses of UV radiation. In sharp contrast, the capacity of vesicular stomatitis virus to shut off cellular transcription was quite resistant to UV radiation. The data presented here indicate that viral transcription is essential to inhibit host RNA metabolism, even though synthesis of viral polypeptides in the inhibited cells could not be detected. At those levels of UV radiation that inactivated all viral gene functions, except viral inhibition of cellular RNA synthesis, the only viral product detected was non-adenylated, low-molecular-weight RNA species.
采用紫外线照射传染性水疱性口炎病毒,以研究小鼠骨髓瘤(MPC - 11)细胞中某些病毒基因功能的表达与病毒对RNA合成的抑制作用之间的关系。病毒感染性、蛋白质合成和病毒mRNA合成均对紫外线辐射高度敏感;然而,在接受大剂量紫外线辐射的病毒制剂中,体外检测到了低水平的病毒转录酶活性。与之形成鲜明对比的是,水疱性口炎病毒关闭细胞转录的能力对紫外线辐射相当耐受。此处呈现的数据表明,病毒转录对于抑制宿主RNA代谢至关重要,尽管在受抑制的细胞中未检测到病毒多肽的合成。在那些使所有病毒基因功能失活(除病毒对细胞RNA合成的抑制作用外)的紫外线辐射水平下,检测到的唯一病毒产物是非腺苷化的低分子量RNA种类。