Wigand R, Gelderblom H, Ozel M, Distler H, Adrian T
Arch Virol. 1983;76(4):307-19. doi: 10.1007/BF01311198.
Adenovirus 8 (Ad 8, strain 1127) has the general structural features of an adenovirus; it produces the genus-specific hexon antigen. The fiber length of 12 nm corresponds to that of other subgenus D adenoviruses. In hemagglutination-inhibition, Ad 8 is related to Ad9 and Ad 15/H9. The slow multiplication, compared to most other subgenus D viruses, was shown not to be caused by an extended growth cycle, but appears to be due to an inefficient virus release into the medium. After restriction analysis with the enzymes Sma I and Bgl II, the typical fragment patterns of species from subgenus D were obtained, while very different patterns emerged from the analysis with Hind III, Bam HI, and Bst E II endonucleases. Several strains of Ad 8 produced more penton-associated toxin than Ad 15/H9 used as reference virus from subgenus D, which could explain the "clumping CPE" caused by Ad 8. Ad 8 toxin was neutralized by antisera from many adenovirus species. The poor virus yield of Ad 8 was not improved by removing soluble viral or cellular substances; all other attempts to improve virus yield by varying the conditions of cell culture also failed.
腺病毒8型(Ad 8,毒株1127)具有腺病毒的一般结构特征;它能产生属特异性六邻体抗原。12纳米的纤维长度与其他D亚属腺病毒的纤维长度相当。在血凝抑制试验中,Ad 8与Ad9和Ad 15/H9相关。与大多数其他D亚属病毒相比,Ad 8增殖缓慢,这并非由于生长周期延长所致,而是似乎归因于病毒向培养基中的释放效率低下。在用Sma I和Bgl II酶进行限制性分析后,获得了D亚属各物种的典型片段模式,而在用Hind III、Bam HI和Bst E II核酸内切酶进行分析时出现了非常不同的模式。与用作D亚属参考病毒的Ad 15/H9相比,几种Ad 8毒株产生了更多与五邻体相关的毒素,这可以解释Ad 8引起的“聚集性细胞病变效应”。Ad 8毒素被许多腺病毒物种的抗血清中和。去除可溶性病毒或细胞物质并不能提高Ad 8的病毒产量;通过改变细胞培养条件来提高病毒产量的所有其他尝试也均告失败。