Wanger A R, Dunny G M
Infect Immun. 1987 May;55(5):1170-5. doi: 10.1128/iai.55.5.1170-1175.1987.
Immunoblotting was used to analyze the immune response of cows to Streptococcus agalactiae. Antibody from the milk of cows immunized (via the superficial inguinal lymph node) with formalinized S. agalactiae cells or from the milk of cows with S. agalactiae mastitis reacted strongly with a group of high-molecular-weight proteinaceous antigens. The two most predominant antigenic polypeptides in this group had apparent molecular weights of 97,000 and 104,000. Because the data indicated that these two antigens, as well as several minor antigens sometimes observed in the 70- to 100-kilodalton size range, seemed to be different forms of the same protein, we refer to the entire group as Sas97/104. A monoclonal antibody that was reactive with Sas97/104 was derived and was used to purify the antigen by affinity chromatography. Whole-cell and colony blot enzyme-linked immunoassays with either the monoclonal antibody or a polyclonal serum sample raised against the affinity-purified antigen indicated that this antigen (or cross-reactive proteins with higher molecular weights) is present on the S. agalactiae strains that were freshly isolated from mastitic cows. However, the antigen was not detected in S. agalactiae of human origin, bovine strains of S. agalactiae maintained for a prolonged period in the laboratory, or other streptococci. The data are consistent with the notion that Sas97/104 is a surface antigen and does not correspond to previously described type-specific antigens of group B streptococci.
免疫印迹法用于分析奶牛对无乳链球菌的免疫反应。用福尔马林处理的无乳链球菌细胞免疫(通过腹股沟浅淋巴结)的奶牛乳汁中的抗体,或患有无乳链球菌乳腺炎的奶牛乳汁中的抗体,与一组高分子量蛋白质抗原发生强烈反应。该组中两种最主要的抗原多肽的表观分子量分别为97,000和104,000。因为数据表明这两种抗原以及有时在70至100千道尔顿大小范围内观察到的几种次要抗原似乎是同一蛋白质的不同形式,所以我们将整个组称为Sas97/104。获得了一种与Sas97/104反应的单克隆抗体,并用于通过亲和层析纯化抗原。用单克隆抗体或针对亲和纯化抗原产生的多克隆血清样本进行的全细胞和菌落印迹酶联免疫测定表明,这种抗原(或具有更高分子量的交叉反应蛋白)存在于从患乳腺炎奶牛新鲜分离的无乳链球菌菌株上。然而,在人源无乳链球菌、在实验室中长期保存的牛源无乳链球菌菌株或其他链球菌中未检测到该抗原。这些数据与Sas97/104是一种表面抗原且与先前描述的B族链球菌型特异性抗原不符的观点一致。