Motzel S L, Riley L K
Department of Veterinary Pathology, University of Missouri, Columbia 65211.
J Clin Microbiol. 1991 Nov;29(11):2566-70. doi: 10.1128/jcm.29.11.2566-2570.1991.
Purified flagella from multiple isolates of Bacillus piliformis were obtained and examined by electron microscopy. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blot (immunoblot) analyses were used to assess the purity, antigenicity, and cross-reactivity of purified flagellar preparations. SDS-PAGE demonstrated a single, major protein band evident at approximately 53 to 56 kDa in all isolates tested. Results of Western blot analyses indicated a lack of cross-reactivity between flagellar antigens and heterologous isolates. Enzyme-linked immunosorbent assays (ELISAs) were used to compare the efficacies of flagellar preparations from the various isolates as antigens in detecting B. piliformis serum antibodies from several host species. ELISA results indicated that no single flagellar preparation could be relied on to consistently identify serum antibodies in all the host species tested; however, ELISAs that utilized a trivalent flagellar antigen preparation were shown to be specific and sensitive for the detection of antibodies to B. piliformis.
从多株丝状芽孢杆菌中获取纯化的鞭毛,并通过电子显微镜进行检查。采用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质免疫印迹(免疫印迹)分析来评估纯化鞭毛制剂的纯度、抗原性和交叉反应性。SDS-PAGE显示,在所有测试菌株中均出现一条明显的主要蛋白带,分子量约为53至56 kDa。蛋白质免疫印迹分析结果表明,鞭毛抗原与异源菌株之间缺乏交叉反应性。使用酶联免疫吸附测定(ELISA)比较来自不同菌株的鞭毛制剂作为抗原检测几种宿主物种丝状芽孢杆菌血清抗体的效果。ELISA结果表明,没有单一的鞭毛制剂能够始终如一地识别所有测试宿主物种中的血清抗体;然而,使用三价鞭毛抗原制剂的ELISA对丝状芽孢杆菌抗体的检测具有特异性和敏感性。