Furze J, Wertz G, Lerch R, Taylor G
AFRC Institute for Animal Health, Compton Laboratory, Berkshire, U.K.
J Gen Virol. 1994 Feb;75 ( Pt 2):363-70. doi: 10.1099/0022-1317-75-2-363.
A panel of 23 monoclonal antibodies (MAbs) specific for the attachment (G) glycoprotein of bovine respiratory syncytial virus (BRS virus), recognizing seven antigenic areas on the G protein, was used to determine the antigenic heterogeneity among 19 BRS viruses isolated over a 20 year period from various parts of the world. The pattern of reactivity of the isolates, as determined by ELISA, identified two major subgroups of BRSV. This finding was confirmed by radioimmunoprecipitation of the G protein by the MAbs and was also demonstrated using polyclonal sera obtained from calves hyperimmunized with BRS virus strains from each subgroup. The subgroups could also be differentiated by differences in the apparent M(r) of the fusion (F) glycoprotein and its cleavage products. The apparent M(r)s of the F0, F1 and F2 polypeptides were 73K, 46K and 17K for subgroup A strains and 77K, 46K and 23K for subgroup B strains. These studies provide evidence for two major lineages of BRS virus, similar to the situation with human RS virus.
一组针对牛呼吸道合胞病毒(BRS病毒)附着(G)糖蛋白的23种单克隆抗体(MAb),可识别G蛋白上的七个抗原区域,用于确定在20年期间从世界各地分离的19株BRS病毒之间的抗原异质性。通过ELISA确定的分离株反应模式,确定了BRSV的两个主要亚组。MAb对G蛋白的放射免疫沉淀证实了这一发现,并且使用从用每个亚组的BRS病毒株进行超免疫的小牛获得的多克隆血清也证明了这一点。亚组之间还可以通过融合(F)糖蛋白及其裂解产物的表观M(r)差异来区分。对于A亚组毒株,F0、F1和F2多肽的表观M(r)分别为73K、46K和17K,对于B亚组毒株分别为77K、46K和23K。这些研究为BRS病毒的两个主要谱系提供了证据,类似于人类呼吸道合胞病毒的情况。