Buller R M, Straus S E, Rose J A
J Gen Virol. 1979 Jun;43(3):663-72. doi: 10.1099/0022-1317-43-3-663.
Human adenovirus (Ad) serotypes provide an early factor(s) that is necessary for adenovirus-associated virus (AAV) multiplication in human cell lines. However, little, if any, AAV production occurs in primary African green monkey kidney (AGMK) cells co-infected with AAV and a helper human Ad (non-permissive infection), unless cells are additionally infected with SV40 (permissive infection). To determine the basis of the host restriction of AAV replication in AGMK cells, AAV DNA, RNA and protein synthesis were analyzed under various conditions of infection. Hybridization reactions revealed no detectable AAV-specific DNA or RNA in infections with AAV alone or in combination with SV40. In co-infections with AAV and Ad5 or Ad7, the synthesis of both AAV- and Ad-specific DNA and RNA occurred without a significant rise in titre of either virus. During non-permissive infection, however, AAV DNA synthesis was abnormal in that an expected accumulation of single-stranded progeny molecules was not observed. Finally, although intact 20S AAV transcripts were present in the cytoplasm of AGMK cells during non-permissive infection (in amounts ranging from 50 to 80% of that found during permissive infection), AAV-specific polypeptides were not demonstrable by polyacrylamide gel electrophoresis. Taken together, these experiments indicate that the host restriction of AAV replication in AGMK cells is exerted at the level of translation of the single AAV messenger RNA. In addition, it appears that one or more of the AAV polypeptides specified by this message is required for the production of single-stranded AAV progeny DNA.
人类腺病毒(Ad)血清型提供了腺病毒相关病毒(AAV)在人类细胞系中增殖所必需的早期因子。然而,在与AAV和辅助人类Ad共同感染的原代非洲绿猴肾(AGMK)细胞中(非允许性感染),几乎没有AAV产生,除非细胞另外感染SV40(允许性感染)。为了确定AGMK细胞中AAV复制的宿主限制基础,在各种感染条件下分析了AAV的DNA、RNA和蛋白质合成。杂交反应显示,单独感染AAV或与SV40联合感染时,未检测到AAV特异性DNA或RNA。在AAV与Ad5或Ad7共同感染时,AAV和Ad特异性DNA和RNA的合成均发生,而两种病毒的滴度均未显著升高。然而,在非允许性感染期间,AAV DNA合成异常,因为未观察到预期的单链子代分子积累。最后,尽管在非允许性感染期间AGMK细胞的细胞质中存在完整的20S AAV转录本(其数量为允许性感染期间的50%至80%),但通过聚丙烯酰胺凝胶电泳无法检测到AAV特异性多肽。综上所述,这些实验表明,AGMK细胞中AAV复制的宿主限制作用于单一AAV信使RNA的翻译水平。此外,似乎由该信使指定的一种或多种AAV多肽是产生单链AAV子代DNA所必需的。