Lung N P, Thompson J P, Kollias G V, Klein P A
Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville 32610, USA.
Am J Vet Res. 1996 Aug;57(8):1157-61.
To produce monoclonal antibodies (MAB) with specificity for the heavy chain of macaw IgG; to incorporate these MAB into an ELISA to measure IgG responses of macaws inoculated with bovine serum albumin (BSA); and to evaluate the antigenicity of BSA in Blue and Gold Macaws.
Four 1-year-old Blue and Gold Macaws, 2 males and 2 females.
1 male and 1 female 1 were randomly assigned to each of 2 study groups. Group-1 birds were inoculated with 200 micrograms of BSA on days 0, 14, 28, and 42. Group-2 birds were inoculated with 200 micrograms of BSA on days 0 and 28. Blood was collected weekly for measurement of anti-BSA titer. Hybridomas were prepared from mice immunized with Scarlet Macaw (Ara macao) IgG purified by salt precipitation and gel chromatography. Specificity for IgG of Scarlet Macaw and other macaw species was confirmed by ELISA and western blot analysis. Hybridoma HL544 was cloned and the antibody purified. Following biotinylation, MAB HL544 was incorporated into an ELISA that measured IgG responses of macaws inoculated with BSA.
Adult Blue and Gold Macaws developed strong primary and secondary anti-BSA antibody titers 14 days after inoculation with 200 micrograms of BSA. An inoculation interval of 28 days resulted in stronger secondary responses than an interval of only 14 days.
MAB specific for macaw immunoglobulins can be used in ELISA to evaluate the humoral immune responses of macaws. 1-year-old Blue and Gold Macaws developed strong anti-BSA titer when inoculated with 200 micrograms of BSA. An inoculation interval of 28 days resulted in stronger secondary responses than did an interval of only 14 days.
These MAB, the first reported to have specificity for a psittacine antibody class, will be useful in the evaluation of psittacine antibody responses and in the development of psittacine diagnostic assays.
制备对金刚鹦鹉IgG重链具有特异性的单克隆抗体(MAB);将这些单克隆抗体整合到酶联免疫吸附测定(ELISA)中,以检测接种牛血清白蛋白(BSA)的金刚鹦鹉的IgG反应;并评估蓝黄金刚鹦鹉中BSA的抗原性。
4只1岁的蓝黄金刚鹦鹉,2只雄性和2只雌性。
将1只雄性和1只雌性随机分配到2个研究组中的每组。第1组的鸟在第0、14、28和42天接种200微克BSA。第2组的鸟在第0和28天接种200微克BSA。每周采集血液以测量抗BSA滴度。用通过盐沉淀和凝胶色谱法纯化的绯红金刚鹦鹉(Ara macao)IgG免疫小鼠制备杂交瘤。通过ELISA和蛋白质印迹分析确认对绯红金刚鹦鹉和其他金刚鹦鹉物种IgG的特异性。克隆杂交瘤HL544并纯化抗体。生物素化后,将单克隆抗体HL544整合到ELISA中,该ELISA用于检测接种BSA的金刚鹦鹉的IgG反应。
成年蓝黄金刚鹦鹉在接种200微克BSA后14天产生强烈的初次和二次抗BSA抗体滴度。28天的接种间隔比仅14天的间隔产生更强的二次反应。
对金刚鹦鹉免疫球蛋白具有特异性的单克隆抗体可用于ELISA,以评估金刚鹦鹉的体液免疫反应。1岁的蓝黄金刚鹦鹉接种200微克BSA时产生强烈的抗BSA滴度。28天的接种间隔比仅14天的间隔产生更强的二次反应。
这些单克隆抗体是首次报道对鹦鹉抗体类别具有特异性,将有助于鹦鹉抗体反应的研究以及鹦鹉诊断检测方法的开发。