Horzinek M, Keldermans L, Stuurman T, Black J, Herrewegh A, Sillekens P, Koolen M
Department of Virology, Veterinary Faculty, State University of Utrecht, The Netherlands.
J Gen Virol. 1991 Dec;72 ( Pt 12):2923-8. doi: 10.1099/0022-1317-72-12-2923.
Bovine immunodeficiency virus (BIV) was purified by isodensity centrifugation; viral activities were monitored in gradient fractions using the reverse transcriptase assay and a p26-specific monoclonal antibody ELISA. In the coincident peak fractions (density about 1.17 g/ml) proteins with Mr values of 26K, 17K, 53K, 14K and 100K (with decreasing intensity) were detected by Western blotting using serum of a calf after experimental BIV infection. When 957 randomly collected cattle sera from The Netherlands were tested by indirect immunofluorescence and confirmed using Western blot and/or radioimmunoprecipitation, 1.4% appeared seropositive. Thus BIV infection is not uncommon in one European cattle population.
牛免疫缺陷病毒(BIV)通过等密度离心法进行纯化;使用逆转录酶测定法和p26特异性单克隆抗体酶联免疫吸附测定法(ELISA)对梯度级分中的病毒活性进行监测。在重叠的峰值级分(密度约为1.17 g/ml)中,通过使用实验性感染BIV后的小牛血清进行蛋白质印迹法,检测到分子量为26K、17K、53K、14K和100K(强度递减)的蛋白质。当用间接免疫荧光法检测来自荷兰的957份随机采集的牛血清,并使用蛋白质印迹法和/或放射免疫沉淀法进行确认时,1.4%的血清呈阳性。因此,BIV感染在一个欧洲牛群中并不罕见。