Efstratiou A, Maxted W R
J Clin Pathol. 1979 Dec;32(12):1228-33. doi: 10.1136/jcp.32.12.1228.
Streptococcal grouping sera for groups A, B, C, and G prepared for conventional testing by precipitation were made specific by absorption and used to identify streptococci by slide agglutination with and without staphyloccocal coagglutination. Trypsinised suspensions of 1055 strains, identified by precipitation as belonging to group A, B, C, or G, were tested by slide agglutination. Of these, 998 were correctly identified using a streptococcal suspension and antisera alone and a further 65 were identified when a loopful of protein A-positive staphylococci was added. Suspensions of 88 strains not of groups A, B, C, or G gave no reaction in the agglutination test with or without the addition of staphylococci. Group polysaccharide extracted by conventional methods also caused agglutination of staphylococci on a slide when specific antiserum was added. Growth from primary or secondary cultures digested in streptomyces enzyme for only 15-30 minutes provided an excellent antigen for a quick and simple method of streptococcal grouping using non-sensitised staphylococcal suspension and specific antisera for coagglutination.
通过沉淀法制备的用于常规检测的A、B、C和G群链球菌分组血清,经吸收后具有特异性,并用于通过玻片凝集试验(有无葡萄球菌协同凝集)鉴定链球菌。对1055株经沉淀法鉴定为属于A、B、C或G群的菌株制成的胰蛋白酶消化悬液进行玻片凝集试验。其中,仅使用链球菌悬液和抗血清时,998株被正确鉴定,另外添加一满环蛋白A阳性葡萄球菌时,又有65株被鉴定出来。88株不属于A、B、C或G群的菌株悬液,无论是否添加葡萄球菌,在凝集试验中均无反应。用常规方法提取的群多糖,加入特异性抗血清后,在玻片上也能引起葡萄球菌凝集。在链霉菌酶中消化15 - 30分钟的初代或次代培养物生长物,为使用未致敏葡萄球菌悬液和特异性抗血清进行协同凝集的快速简便的链球菌分组方法提供了优良抗原。