Iwata A, Consigli R A
J Virol. 1971 Jan;7(1):29-40. doi: 10.1128/JVI.7.1.29-40.1971.
The addition of phleomycin (25 mug) to primary mouse embryo cells infected with polyoma virus was found to cause 96% inhibition of the synthesis of infectious virus. When ribonucleic acid and protein synthesis was investigated in these cells by use of isotope incorporation, it was found that neither was inhibited drastically. Immunofluorescent staining studies with the use of antibody directed to the viral structural proteins showed that proteins were synthesized in the presence of the antibiotic. However, when deoxyribonucleic acid (DNA) synthesis was investigated, it was found that DNA synthesis in uninfected cells was completely inhibited within the initial 10 hr of phleomycin addition, whereas DNA synthesis in infected cells proceeded at a reduced rate. Selective DNA extraction (Hirt method) of phleomycin-treated infected cells demonstrated that synthesized viral DNA was salt-extractable, similar to that in infected control cells lacking phleomycin. This extracted DNA was further fractionated by ethidium bromide-cesium chloride density gradient equilibrium centrifugation. The phleomycin-treated preparations revealed twice as much component II (circular nicked and linear) as component I (supercoiled) DNA, whereas the DNA from normally infected control cells showed the reverse picture. It was also demonstrated that viral particles synthesized in the presence of phleomycin did not contain component I DNA. This packaged DNA was found to consist of fragments of both the host and viral types. Cells that were prelabeled with (3)H-thymidine and then treated with phleomycin demonstrated host DNA degradation. However, fragments formed from prelabeled host DNA were not encapsidated into viral particles.
研究发现,向感染多瘤病毒的原代小鼠胚胎细胞中添加博来霉素(25微克)可使感染性病毒的合成受到96%的抑制。当通过同位素掺入法研究这些细胞中的核糖核酸和蛋白质合成时,发现两者均未受到严重抑制。使用针对病毒结构蛋白的抗体进行免疫荧光染色研究表明,在抗生素存在的情况下蛋白质仍可合成。然而,当研究脱氧核糖核酸(DNA)合成时,发现添加博来霉素后的最初10小时内,未感染细胞中的DNA合成完全受到抑制,而感染细胞中的DNA合成则以较低的速率进行。对经博来霉素处理的感染细胞进行选择性DNA提取(赫特方法)表明,合成的病毒DNA可被盐提取,这与缺乏博来霉素的感染对照细胞中的情况相似。将这种提取的DNA进一步通过溴化乙锭-氯化铯密度梯度平衡离心进行分级分离。经博来霉素处理的制剂显示,组分II(环状切口和线性)的DNA是组分I(超螺旋)DNA的两倍,而正常感染对照细胞的DNA情况则相反。还证明,在博来霉素存在下合成的病毒颗粒不含组分I DNA。这种包装的DNA被发现由宿主和病毒类型的片段组成。用(3)H-胸腺嘧啶核苷预先标记然后用博来霉素处理的细胞显示出宿主DNA降解。然而,由预先标记的宿主DNA形成的片段并未被包装到病毒颗粒中。