Czifra G, Tuboly T, Sundquist B G, Stipkovits L
Veterinary Medical Research Institute, Budapest, Hungary.
Avian Dis. 1993 Jul-Sep;37(3):689-96.
Monoclonal antibodies (MAbs) were prepared to study the immunogenesis of Mycoplasma gallisepticum. Balb/c mice were immunized with M. gallisepticum immunostimulating complexes and the supernatant of heterokaryotes screened with M. gallisepticum and closely related M. synoviae as antigens in indirect enzyme-linked immunosorbent assay. All selected MAbs proved to be M. gallisepticum species-specific when they were tested against 10 different avian Mycoplasma species. After immunoblotting analysis, five polypeptides were identified with estimated molecular weights of 110,000, 66,000, 64,000, 56,000, and 50,000. Cell membrane localization of the recognized polypeptides was studied by immunoelectron microscopy. None of the MAbs inhibited the hemagglutinating activity of freshly prepared M. gallisepticum. However, one MAb (B3) specific for p56 agglutinated the stained M. gallisepticum antigen in the slide agglutination test. Results seemed to correlate with published information on the protein composition and agglutinating activity of Mycoplasma gallisepticum.
制备单克隆抗体(MAb)以研究鸡毒支原体的免疫发生。用鸡毒支原体免疫刺激复合物以及以鸡毒支原体和密切相关的滑液支原体作为抗原在间接酶联免疫吸附测定中筛选的异核体上清液免疫Balb/c小鼠。当针对10种不同的禽支原体物种进行测试时,所有选定的单克隆抗体均被证明是鸡毒支原体物种特异性的。经过免疫印迹分析,鉴定出5种多肽,估计分子量分别为110,000、66,000、64,000、56,000和50,000。通过免疫电子显微镜研究了识别多肽的细胞膜定位。没有一种单克隆抗体抑制新鲜制备的鸡毒支原体的血凝活性。然而,一种针对p56的单克隆抗体(B3)在玻片凝集试验中凝集了染色的鸡毒支原体抗原。结果似乎与关于鸡毒支原体蛋白质组成和凝集活性的已发表信息相关。