Björkman C, Holmdahl O J, Uggla A
Dept. Cattle and Sheep Diseases, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Vet Parasitol. 1997 Feb;68(3):251-60. doi: 10.1016/s0304-4017(96)01076-x.
An indirect enzyme-linked immunosorbent assay (ELISA) for detection of antibodies to Neospora caninum in serum from cattle is described. Extracted tachyzoite proteins incorporated into immunostimulating complexes (iscoms) were used as coating antigen and a mouse monoclonal antibody to bovine immunoglobulin G1 as conjugate. Western blot analysis of the iscom preparation revealed a restricted number of antigens compared with whole parasite homogenates. When probed with a serum from an experimentally infected calf, heavily stained antigens with apparent molecular masses of 28, 35, 45 and 78 kDa were seen. The sensitivity and specificity of the ELISA was 100% and 96%, respectively, against an indirect fluorescent antibody test as indicator of true status. The applicability of the ELISA for demonstration of antibodies in milk was evaluated and the agreement between serum and milk ELISA was 95%.
本文描述了一种用于检测牛血清中犬新孢子虫抗体的间接酶联免疫吸附测定(ELISA)方法。将提取的速殖子蛋白掺入免疫刺激复合物(iscoms)中作为包被抗原,并使用抗牛免疫球蛋白G1的小鼠单克隆抗体作为共轭物。与整个寄生虫匀浆相比,iscom制剂的蛋白质印迹分析显示抗原数量有限。用实验感染小牛的血清进行检测时,可观察到表观分子量为28、35、45和78 kDa的深色染色抗原。以间接荧光抗体试验作为真实状态的指标,该ELISA的敏感性和特异性分别为100%和96%。评估了该ELISA在检测牛奶中抗体方面的适用性,血清ELISA和牛奶ELISA之间的一致性为95%。