Fernandez-Lago L, Rodriguez-Nebreda M S, Chordi A
Department of Microbiology, Faculty of Pharmacy, University of Salamanca, Spain.
Ann Inst Pasteur Microbiol. 1988 Jul-Aug;139(4):461-71. doi: 10.1016/0769-2609(88)90108-1.
A rapid co-agglutination test using monospecific antisera was developed for the serological typing of enteropathogenic strains of Yersinia enterocolitica. A total of 70 bacterial strains (17 reference strains and 53 clinical isolates) were examined. Absorption of immune sera against serotypes O:3, O:8 and O:9 with their heterologous antigens (S-LPS) was necessary to avoid the appearance of different cross-reactions, as observed by co-agglutination. The proteins present in the S-LPS preparations obtained from each serotype seemed to be responsible for such cross-reactions. Results obtained with a total of 57 clinical isolates belonging to other members of the family Enterobacteriaceae indicate a high specificity of the assay.
开发了一种使用单特异性抗血清的快速协同凝集试验,用于小肠结肠炎耶尔森菌致病菌株的血清学分型。共检测了70株细菌(17株参考菌株和53株临床分离株)。如协同凝集所观察到的,用其异源抗原(S-LPS)吸收针对O:3、O:8和O:9血清型的免疫血清,以避免出现不同的交叉反应。从每种血清型获得的S-LPS制剂中存在的蛋白质似乎是造成这种交叉反应的原因。对总共57株属于肠杆菌科其他成员的临床分离株所获得的结果表明该检测具有高度特异性。