Alderete J F
Infect Immun. 1983 Apr;40(1):284-91. doi: 10.1128/iai.40.1.284-291.1983.
Characterization of immunogenic Trichomonas vaginalis membrane proteins was accomplished by using extrinsically and intrinsically labeled organisms and a highly sensitive and specific radioimmunoprecipitation procedure. Intact motile trichomonads were compared with detergent extracts as a source of antigen in radioimmunoprecipitation experiments. Approximately 20 proteins accessible to antibody were identified and ranged in molecular weight from 200,000 to 20,000. Localization on the parasite surface of the highly immunogenic membrane proteins was attempted by using, as the indicator system, formaldehyde-fixed protein A-bearing Staphylococcus aureus pretreated with the various antiserum reagents and incubated with live, motile parasites. Also, indirect immunofluorescence with fluorescein isothiocyanate--anti-rabbit immunoglobulin was also employed after incubation of organisms with either control serum or antiserum from immunized rabbits or after treatment of trichomonads with the immunoglobulin G fraction from each respective serum. No immunoglobulin G antibody appeared to be directed at the anterior trichomonal flagella or the posterior axostyle, whereas strong fluorescence was detected throughout the rest of the T. vaginalis surface. The biological significance of these data is discussed.
通过使用外在和内在标记的生物体以及高度灵敏和特异的放射免疫沉淀程序,对具有免疫原性的阴道毛滴虫膜蛋白进行了表征。在放射免疫沉淀实验中,将完整的活动滴虫与去污剂提取物作为抗原来源进行了比较。鉴定出约20种可与抗体结合的蛋白质,其分子量范围为200,000至20,000。通过使用经各种抗血清试剂预处理并与活的活动寄生虫孵育的甲醛固定的含蛋白A金黄色葡萄球菌作为指示系统,尝试确定高免疫原性膜蛋白在寄生虫表面的定位。此外,在用对照血清或免疫兔的抗血清孵育生物体后,或在用来自各自血清的免疫球蛋白G组分处理滴虫后,还采用了异硫氰酸荧光素 - 抗兔免疫球蛋白进行间接免疫荧光检测。似乎没有免疫球蛋白G抗体针对滴虫前部的鞭毛或后部的轴柱,而在阴道毛滴虫表面的其余部分检测到强荧光。讨论了这些数据的生物学意义。