Jackson S G, Yip-Chuck D A, Brodsky M H
J Immunol Methods. 1985 Oct 24;83(1):141-50. doi: 10.1016/0022-1759(85)90067-5.
A double antibody sandwich enzyme-immunoassay has been developed for detection of Clostridium perfringens enterotoxin. Anti-enterotoxin immunoglobulin G-alkaline phosphatase conjugates were prepared using a rapid minicolumn procedure. The assay can achieve a sensitivity of greater than or equal to 1 ng/ml with purified enterotoxin. Sensitivity for detection of cases of C. perfringens enteritis in a C. perfringens outbreak (86 individuals tested) was between 85.7 and 98.0 per cent depending upon stringency of criteria for defining positive cases. Specificity of the assay was demonstrated by the lack of positive results in 53 individuals involved in a gastroenteritis outbreak of unknown etiology.
已开发出一种双抗体夹心酶免疫测定法用于检测产气荚膜梭菌肠毒素。采用快速微柱法制备抗肠毒素免疫球蛋白G-碱性磷酸酶结合物。该测定法对纯化的肠毒素可达到大于或等于1纳克/毫升的灵敏度。在产气荚膜梭菌暴发(检测了86人)中检测产气荚膜梭菌肠炎病例的灵敏度,根据定义阳性病例的标准严格程度,在85.7%至98.0%之间。在53名涉及不明病因肠胃炎暴发的个体中未得到阳性结果,证明了该测定法的特异性。