Silverstein G, Strohl W A
Arch Virol. 1986;87(3-4):241-64. doi: 10.1007/BF01315303.
The nature of the infection of mouse B3T3 cells by adenovirus type 2 (Ad2) has been studied in vitro. Following infection with an adsorbed MOI of 225, more than 90 percent of the cells synthesized both early and late virus-specific antigens. In contrast, the yield of progeny virus varied from only 2 X 10(4) to 2 X 10(6) FFU/2 X 10(5) cells. The range in yields was related, in part, to the number of cell generations from the time of the initial subcloning, the yield increasing with passage level. Infectious center analysis suggested that fewer than 0.5 percent of infected cells synthesized progeny virus. Analysis of DNA synthesis in infected multiplying B3T3 cells demonstrated that cellular DNA synthesis began to be shut off at 12 hours p.i., a time when viral DNA synthesis was beginning. The maximum rate of viral DNA synthesis was approximately 12 percent of that in infected human cells. In contrast to infected multiplying cells, infection of quiescent B3T3 cell cultures resulted in the induction of cellular, along with viral, DNA synthesis. Analysis of late gene expression detected synthesis of most viral polypeptides, but revealed greater than 90 percent reductions in the rate of synthesis of polypeptides II, III, IV, and IX, as compared with infected human cells.
对2型腺病毒(Ad2)感染小鼠B3T3细胞的性质进行了体外研究。以225的吸附感染复数进行感染后,超过90%的细胞合成了早期和晚期病毒特异性抗原。相比之下,子代病毒的产量仅在2×10⁴至2×10⁶空斑形成单位/2×10⁵个细胞之间变化。产量范围部分与从最初亚克隆时起的细胞代数有关,产量随传代水平增加。感染中心分析表明,不到0.5%的感染细胞合成子代病毒。对感染的增殖性B3T3细胞中的DNA合成分析表明,细胞DNA合成在感染后12小时开始关闭,此时病毒DNA合成开始。病毒DNA合成的最大速率约为感染人类细胞的12%。与感染的增殖细胞相反,静止的B3T3细胞培养物感染后导致细胞DNA合成以及病毒DNA合成的诱导。对晚期基因表达的分析检测到大多数病毒多肽的合成,但与感染人类细胞相比,多肽II、III、IV和IX的合成速率降低了90%以上。