{"title":"A sandwich ELISA method for detection of Staphylococcus aureus enterotoxins.","authors":"B P Berdal, O Olsvik, T Omland","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Staphylococcus aureus enterotoxins A, B, and C, were detected by means of a four-layer sandwich ELISA method. With toxin produced in broth supernatants, this ELISA method had a detection limit of 0.5 ng enterotoxin per ml. Conjoint with enterotoxin, S. aureus most often produces protein A. The protein A will interfere and produce false positive reactions in a sandwich ELISA, by binding nonspecifically the IgG in different layers, simulating the immunospecific toxin binding. With rabbit IgG coupled to Sepharose CL-4B gel, 99% of protein A could be removed from solutions, bringing the level under the interfering limit in the ELISA.</p>","PeriodicalId":75410,"journal":{"name":"Acta pathologica et microbiologica Scandinavica. Section B, Microbiology","volume":"89 6","pages":"411-5"},"PeriodicalIF":0.0000,"publicationDate":"1981-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta pathologica et microbiologica Scandinavica. Section B, Microbiology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Staphylococcus aureus enterotoxins A, B, and C, were detected by means of a four-layer sandwich ELISA method. With toxin produced in broth supernatants, this ELISA method had a detection limit of 0.5 ng enterotoxin per ml. Conjoint with enterotoxin, S. aureus most often produces protein A. The protein A will interfere and produce false positive reactions in a sandwich ELISA, by binding nonspecifically the IgG in different layers, simulating the immunospecific toxin binding. With rabbit IgG coupled to Sepharose CL-4B gel, 99% of protein A could be removed from solutions, bringing the level under the interfering limit in the ELISA.
采用四层夹心ELISA法检测金黄色葡萄球菌肠毒素A、B、C。当毒素产生于肉汤上清液时,本ELISA方法的检出限为0.5 ng / ml。金黄色葡萄球菌与肠毒素结合时,最常产生蛋白a,蛋白a在夹心ELISA中通过非特异性结合不同层的IgG,模拟免疫特异性的毒素结合,从而干扰并产生假阳性反应。兔IgG与Sepharose CL-4B凝胶偶联,可去除溶液中99%的蛋白A,使其水平低于ELISA的干扰限。