Peterkin P I, Sharpe A N
Appl Environ Microbiol. 1984 May;47(5):1047-53. doi: 10.1128/aem.47.5.1047-1053.1984.
Based on enzyme-linked immunosorbent assay, a convenient method has been devised for the direct demonstration of enterotoxin B production by Staphylococcus aureus colonies grown for 24 h on membrane filters. The problem of false-positive reactions due to binding of immunoglobulin G to protein A was turned to advantage by conjugating horseradish peroxidase directly to protein A, which then mediated the labeling of the antitoxin. The test requires 3 h to complete and yields a purple stain at the site of enterotoxin B-producing colonies, thus allowing direct enumeration of confirmed S. aureus in foods within 27 h. The method should be applicable to other enterotoxins of S. aureus.
基于酶联免疫吸附测定法,已设计出一种简便方法,可直接证明在膜滤器上生长24小时的金黄色葡萄球菌菌落产生的肠毒素B。通过将辣根过氧化物酶直接与蛋白A偶联,利用免疫球蛋白G与蛋白A结合导致的假阳性反应问题,蛋白A随后介导抗毒素的标记。该检测需要3小时完成,并在产生肠毒素B的菌落部位产生紫色染色,从而能够在27小时内直接计数食品中经确认的金黄色葡萄球菌。该方法应适用于金黄色葡萄球菌的其他肠毒素。