Kathmann P, Schick J, Winnacker E L, Doerfler W
J Virol. 1976 Jul;19(1):43-53. doi: 10.1128/JVI.19.1.43-53.1976.
Fourteen temperature-sensitive mutants of human adenovirus type2, which differed in their plaquing efficiencies at at the permissive and nonpermissive temperatures by 4 to 5 orders of magnitude, were isolated. These mutants, which could be assigned to seven complementation groups, were tested for their capacity to synthesize adenovirus DNA at the nonpermissive temperature. Three mutants in three different complementation groups proved deficient in viral DNA synthesis. The DNA-negative mutant H2ts206 complemented the DNA-negative mutants H5ts36 and H5ts125, whereas mutant H2ts201 complemented H5ts36 only. Among the DNA-negative mutants, H2ts206 synthesized the smallest amount of viral DNA at the nonpermissive temperature (39.5 C). Data obtained in temperature shift experiments indicated that a very early function was involved in temperature sensitivity. In keeping with this observation, early virus-specific mRNA was not detected in cells infected with H2ts206 and maintained at 39.5 C. Prolonged (52 h) incubation of cells infected with H2ts206 at the nonpermissive temperature led to the synthesis of a high-molecular-weight form of viral DNA.
分离出了14种人腺病毒2型的温度敏感突变体,它们在允许温度和非允许温度下的空斑形成效率相差4到5个数量级。这些可分为7个互补组的突变体,在非允许温度下测试了它们合成腺病毒DNA的能力。三个不同互补组中的三个突变体被证明在病毒DNA合成方面存在缺陷。DNA阴性突变体H2ts206能互补DNA阴性突变体H5ts36和H5ts125,而突变体H2ts201仅能互补H5ts36。在DNA阴性突变体中,H2ts206在非允许温度(39.5℃)下合成的病毒DNA量最少。温度转换实验获得的数据表明,温度敏感性涉及一个非常早期的功能。与此观察结果一致,在感染H2ts206并维持在39.5℃的细胞中未检测到早期病毒特异性mRNA。在非允许温度下用H2ts206感染细胞并延长培养(52小时)导致合成了高分子量形式的病毒DNA。