Ansorg R, Knoche M
Eur J Clin Microbiol. 1984 Jun;3(3):190-4. doi: 10.1007/BF02014876.
Determination of the somatic (O-) antigens of Pseudomonas aeruginosa by conventional slide agglutination is frequently complicated by the barely discernible, slow reaction of native cells. For diagnostic purposes a more practical procedure, a coagglutination test, has been developed in which protein A bearing Staphylococcus aureus (ATCC 12598) cells are added to the agglutination process occurring between specific anti-O serum and native Pseudomonas aeruginosa. Compared to the conventional method, slide O-coagglutination yields larger agglutinates in a shorter mean reaction time, i.e. one minute vs four minutes. Moreover, strains not reacting in the O-agglutination method or reacting only with polyvalent anti-O serum can be grouped by O-coagglutination, and cross reactions between reference strains of different O-groups do not occur. This method facilitates O-grouping of Pseudomonas aeruginosa in epidemiological investigations.
通过传统玻片凝集法测定铜绿假单胞菌的体细胞(O-)抗原,常常因天然细胞难以察觉的缓慢反应而变得复杂。为了诊断目的,已开发出一种更实用的方法——协同凝集试验,即将携带蛋白A的金黄色葡萄球菌(ATCC 12598)细胞加入到特异性抗O血清与天然铜绿假单胞菌之间发生的凝集过程中。与传统方法相比,玻片O-协同凝集在更短的平均反应时间内产生更大的凝集物,即分别为1分钟和4分钟。此外,在O-凝集法中不发生反应或仅与多价抗O血清发生反应的菌株可以通过O-协同凝集进行分组,并且不同O群的参考菌株之间不会发生交叉反应。该方法有助于在流行病学调查中对铜绿假单胞菌进行O群分类。