Schnitzlein W M, Ghildyal N, Tripathy D N
Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Illinois, Urbana 61801.
Virus Res. 1988 Apr;10(1):65-75. doi: 10.1016/0168-1702(88)90058-5.
A permanent cell line of avian origin, QT-35, was used for the propagation of avipoxvirus isolates, including juncopox, pigeon pox, and field and vaccine strains of fowlpox viruses. The genomes of these avipoxvirus isolates were compared by restriction enzyme analysis using BamHI and HindIII endonuclease digestion and subsequent agarose gel electrophoresis. The genetic profiles of the virus strains were very similar, with a high proportion of comigrating fragments, although most strains could still be distinguished; therefore, these avipoxviruses appear to be closely related. Similar results were obtained when the immunogenic proteins of 6 fowlpox virus strains were examined by immunoblotting. Although the majority of the antigens were common, the strains could be differentiated by unique proteins of differing electrophoretic mobilities.
一种源自禽类的永久细胞系QT - 35,被用于禽痘病毒分离株的繁殖,这些分离株包括痘病毒、鸽痘病毒以及禽痘病毒的野外毒株和疫苗株。使用BamHI和HindIII内切酶消化以及随后的琼脂糖凝胶电泳,通过限制性酶切分析对这些禽痘病毒分离株的基因组进行了比较。尽管大多数毒株仍可区分,但病毒株的遗传图谱非常相似,共迁移片段比例很高;因此,这些禽痘病毒似乎密切相关。当通过免疫印迹法检测6株禽痘病毒株的免疫原性蛋白时,也获得了类似结果。虽然大多数抗原是共同的,但这些毒株可通过具有不同电泳迁移率的独特蛋白进行区分。