Kern J, Gilden R V, Huebner R J
Appl Microbiol. 1969 Jun;17(6):914-9. doi: 10.1128/am.17.6.914-919.1969.
The intracellular development in acutely infected cells of bovine and canine adenovirus T antigens was followed by immunofluorescent staining. With both species of adenovirus, antigen was first detected as intranuclear pin-points at 18 hr postinfection and coalescence into large lobular masses was noticed by 24 hr. Cross-reactions between bovine 1 (nononcogenic) and bovine 3 (oncogenic) T antigens were not observed by the direct technique although the more sensitive indirect procedure did reveal cross-reactivity. Extensive cross-reactions were observed between the T antigens of the oncogenic canine hepatitis virus and the "nononcogenic" Toronto strain of canine adenovirus. The magnitude of these reactions places the two canine strains in the same T antigen subgroup. The canine and bovine T antigens were not stained by tumor antisera against any of the known human or simian T antigen subgroups. Antigen synthesis was not prevented by inhibitors of deoxyribonucleic acid synthesis although the appearance was altered markedly.
通过免疫荧光染色追踪牛和犬腺病毒T抗原在急性感染细胞中的细胞内发育情况。对于这两种腺病毒,感染后18小时抗原首先被检测为核内的针尖状,到24小时时可观察到其聚合成大的小叶状团块。尽管更灵敏的间接方法确实显示出交叉反应性,但直接技术未观察到牛1型(非致癌性)和牛3型(致癌性)T抗原之间的交叉反应。在致癌性犬肝炎病毒的T抗原与犬腺病毒的“非致癌性”多伦多株之间观察到广泛的交叉反应。这些反应的程度将两种犬病毒株归为同一T抗原亚组。犬和牛的T抗原不会被针对任何已知人类或猿猴T抗原亚组的肿瘤抗血清染色。尽管外观发生了明显改变,但脱氧核糖核酸合成抑制剂并未阻止抗原合成。