Marshall R, Pongparit S, Kaufman A K
Department of Microbiology, California State University, Los Angeles 90032.
Eur J Clin Microbiol. 1987 Aug;6(4):395-401. doi: 10.1007/BF02013093.
The purpose of this investigation was to develop a serological procedure for rapid identification of the following five Bacteroides species: Bacteroides distasonis, Bacteroides fragilis, Bacteroides ovatus, Bacteroides uniformis, and Bacteroides vulgatus. The outer membrane fractions were assayed using SDS-polyacrylamide slab gel electrophoretic techniques. The species-specific protein band from each species as well as the group-specific protein were purified and used to develop an indirect enzyme-linked immunosorbent assay to detect the species-specific and group-specific protein from the outer membrane of five reference species. The sensitivity and specificity of the procedure were evaluated by indirect ELISA methodology using 506 clinical isolates of organisms in this group, ten other species of anaerobic gram-negative bacilli, and three species of aerobic gram-negative bacilli. Each species evaluated yielded unique outer membrane protein patterns, suggesting the potential for development of a rapid, species-specific diagnostic procedure.
本研究的目的是开发一种血清学方法,用于快速鉴定以下五种拟杆菌属细菌:解脲拟杆菌、脆弱拟杆菌、卵形拟杆菌、单形拟杆菌和普通拟杆菌。使用SDS-聚丙烯酰胺平板凝胶电泳技术分析外膜组分。纯化每种细菌的种特异性蛋白条带以及组特异性蛋白,并用于开发间接酶联免疫吸附测定法,以检测五种参考细菌外膜中的种特异性和组特异性蛋白。使用该组中的506株临床分离菌、其他十种厌氧革兰氏阴性杆菌和三种需氧革兰氏阴性杆菌,通过间接ELISA方法评估该方法的敏感性和特异性。所评估的每种细菌都产生了独特的外膜蛋白图谱,表明开发一种快速、种特异性诊断方法具有潜力。