Artamonova V A, Shevliagin V Ia
Vopr Virusol. 1978 Mar-Apr(2):187-92.
The quantitative study of adsorption, elution, and penetration of oncogenic polyoma virus (PV) labeled with 3H-thymidine under the influence of beta-propiolactone-inactivated Sendai virus (SV) was carried out in a permissive culture of mouse embryo fibroblasts and in two nonpermissive cultures of human embryo and chick embryo fibroblasts. In adsorption of PV on permissive and nonpermissive cells SV was found to reduce the amount of the adsorbed virus if used before the adsorption and to have no effect on adsorption upon reverse order of treatment of the cells with the two viruses. SV facilitates elution with 5 mM EDTA of PV adsorbed on both permissive and nonpermissive cells. Under the influence of SV, PV could be eluted from the surface of the permissive cells within 1 hour after adsorption and from the surface of the nonpermissive cells within 5-6 hours. Three hours after PV adsorption on permissive cells, both treated and untreated with SV, most of PV DNA (approximately 60%) was found in the nuclear fraction. At the same time, in the nuclear fraction of nonpermissive cells, treated or untreated with SV, the amount of PV DNA was insignificant (about 13%). The fraction containing large granules isolated from the cells which had been in contact with SV was found to contain approximately 50% of 3H-thymidine label.
在小鼠胚胎成纤维细胞的允许性培养以及人胚胎和鸡胚胎成纤维细胞的两种非允许性培养中,开展了对经β-丙内酯灭活的仙台病毒(SV)影响下用³H-胸腺嘧啶核苷标记的致癌多瘤病毒(PV)的吸附、洗脱和穿透的定量研究。在PV吸附于允许性和非允许性细胞的过程中,发现若在吸附前使用SV,会减少吸附的病毒量,而若两种病毒对细胞的处理顺序相反,则对吸附无影响。SV有助于用5 mM EDTA洗脱吸附于允许性和非允许性细胞上的PV。在SV的影响下,吸附后1小时内PV可从允许性细胞表面洗脱,5 - 6小时内可从非允许性细胞表面洗脱。PV吸附于允许性细胞3小时后,无论是否用SV处理,大部分PV DNA(约60%)存在于细胞核部分。与此同时,在非允许性细胞的细胞核部分,无论是否用SV处理,PV DNA的量都很少(约13%)。从与SV接触过的细胞中分离出的含大颗粒的部分,发现含有约50%的³H-胸腺嘧啶核苷标记。