Sopp P, Hooper L B, Clarke M C, Howard C J, Brownlie J
AFRC Institute for Animal Health, Compton Laboratory, Newbury, Berkshire, U.K.
J Gen Virol. 1994 May;75 ( Pt 5):1189-94. doi: 10.1099/0022-1317-75-5-1189.
Flow cytometry and two-colour immunofluorescence were used to detect cytoplasmic bovine viral diarrhoea virus (BVDV) antigen in leukocytes from viraemic cattle. Monoclonal antibody to the p80 protein of BVDV, a non-structural viral antigen, was used to identify the subpopulations of leukocytes in which viral protein synthesis had occurred. Viral antigen was detected in 23% of peripheral blood mononuclear cells. Monocytes were found to have the highest frequency of infection (35%). A higher proportion of CD2+ T cells (23%) were infected, compared with B cells (11%) or WC1+ gamma delta T cells (11%). No significant differences in percentages of different leukocyte subpopulations in blood were detected in persistently viraemic animals compared with controls.
采用流式细胞术和双色免疫荧光法检测病毒血症牛白细胞中的细胞质牛病毒性腹泻病毒(BVDV)抗原。使用针对BVDV非结构病毒抗原p80蛋白的单克隆抗体来鉴定发生病毒蛋白合成的白细胞亚群。在23%的外周血单核细胞中检测到病毒抗原。发现单核细胞的感染频率最高(35%)。与B细胞(11%)或WC1 + γδ T细胞(11%)相比,CD2 + T细胞的感染比例更高(23%)。与对照组相比,持续病毒血症动物血液中不同白细胞亚群的百分比没有显著差异。