Grodzicker T, Lewis J B, Anderson C W
J Virol. 1976 Aug;19(2):559-71. doi: 10.1128/JVI.19.2.559-571.1976.
Adenovirus type 2 (Ad2) grows 1,000 times less well in monkey cells than in human cells. This defect can be overcome, not only upon co-infection of cells with simian virus 40 (SV40), but also when the relevant part of the SV40 genome is integrated into the adenovirus genome to form an adenovirus-SV40 hybrid virus. We have used the nondefective Ad2-SV40 hybrid virus Ad2+ND1, which contains an insertion of 17% of the SV40 genome, to isolate host-range mutants which are defective in growth on monkey cells although they grow normally on human cells. Like Ad2, these mutants are defective in the synthesis of late proteins in monkey cells. A 30,000-molecular-weight protein (30K), unique to Ad2+ND1-infected cells, can be synthesized in vitro, using Ad2+ND1 mRNA that contains SV40 sequences. 30K is not seen in cells infected with those host-range mutants that are most defective in growth on monkey cells, and translation in vitro of SV40-specific mRNA from these cells produces new unique polypeptides, instead of 30K. Genetic and biochemical analyses indicate that these mutants carry point mutations rather than deletions.
2型腺病毒(Ad2)在猴细胞中的生长情况比在人细胞中差1000倍。这种缺陷不仅可以通过细胞与猴病毒40(SV40)共同感染来克服,而且当SV40基因组的相关部分整合到腺病毒基因组中形成腺病毒-SV40杂交病毒时也可以克服。我们使用了无缺陷的Ad2-SV40杂交病毒Ad2+ND1,它含有17%的SV40基因组插入片段,来分离宿主范围突变体,这些突变体在猴细胞上生长有缺陷,但在人细胞上能正常生长。与Ad2一样,这些突变体在猴细胞中晚期蛋白质的合成存在缺陷。一种分子量为30000的蛋白质(30K),是Ad2+ND1感染细胞所特有的,可以利用含有SV40序列的Ad2+ND1 mRNA在体外合成。在那些在猴细胞上生长缺陷最严重的宿主范围突变体感染的细胞中看不到30K,并且从这些细胞中体外翻译SV40特异性mRNA会产生新的独特多肽,而不是30K。遗传和生化分析表明,这些突变体携带的是点突变而非缺失突变。