Toth T E, Jankura D
Virginia-Maryland Regional College of Veterinary Medicine, Virginia Tech, Blacksburg 24061.
J Virol Methods. 1990 Jan;27(1):113-9. doi: 10.1016/0166-0934(90)90151-5.
The temporal manifestation of bovine parainfluenza-3 virus (BPI3V) proteins in the cytoplasm and on the surface of bovine embryonic lung (BEL) cells was characterized by indirect fluorescent antibody (IFA) and hemadsorption (HAd) assays. Intracellular proteins appeared earliest at 0.5 h post inoculation (p.i.) and the infection spread to virtually all cells by 48 h p.i. Viral proteins on the surface of cells were seen first at 16 h p.i., and by 48 h p.i. the entire cell monolayer was IFA positive. Hundred-fold less virus in the inoculum delayed appearance of the intracellular as well as cell-surface viral proteins by 24 h and allowed the infection of only about 1/3 of the cells by 48 h p.i. Kinetics of the development in the proportion of HAd-positive cells correlated with those of the surface fluorescence-positive cells. Morphology of the manifestation of BPI3V proteins is characterized by microphotography.
通过间接荧光抗体(IFA)和血细胞吸附(HAd)试验,对牛副流感3型病毒(BPI3V)蛋白在牛胚胎肺(BEL)细胞胞质和表面的时间表现进行了表征。接种后(p.i.)最早在0.5小时出现细胞内蛋白,到接种后48小时感染几乎扩散到所有细胞。细胞表面的病毒蛋白最早在接种后16小时出现,到接种后48小时整个细胞单层IFA呈阳性。接种物中病毒数量减少100倍会使细胞内以及细胞表面病毒蛋白的出现延迟24小时,并使接种后48小时仅约1/3的细胞受到感染。HAd阳性细胞比例的发展动力学与表面荧光阳性细胞的动力学相关。通过显微摄影对BPI3V蛋白表现的形态进行了表征。