Laughon B E, Viscidi R P, Gdovin S L, Yolken R H, Bartlett J G
J Infect Dis. 1984 May;149(5):781-8. doi: 10.1093/infdis/149.5.781.
Enzyme immunoassays for detection of Clostridium difficile toxins A and B were developed with use of a double-sandwich microtiter plate format. Each assay was specific for its respective toxin and was sensitive to 0.1 ng of toxin. Neither assay was reactive with 13 other species of clostridia. One hundred fifty fecal specimens submitted for tissue culture cytotoxicity assay were evaluated by enzyme-linked immunosorbent assay (ELISA). Of the 79 tissue culture-positive specimens, 72 (91%) were positive in the A assay, 63 (80%) were positive in the B assay, and 75 (95%) were positive in either assay. Specimens with tissue culture titers of greater than or equal to 10(3) were uniformly positive in both assays. The specificities of the toxin A and B ELISAs were 98.6% and 100%, respectively. An ELISA for both toxins could serve as a substitute for the tissue culture cytotoxicity assay.
采用双夹心微量滴定板形式开发了用于检测艰难梭菌毒素A和B的酶免疫测定法。每种测定法对其相应的毒素具有特异性,对0.1 ng毒素敏感。两种测定法均与其他13种梭菌无反应。通过酶联免疫吸附测定法(ELISA)对150份提交进行组织培养细胞毒性测定的粪便标本进行了评估。在79份组织培养阳性标本中,72份(91%)在A测定法中呈阳性,63份(80%)在B测定法中呈阳性,75份(95%)在任一测定法中呈阳性。组织培养滴度大于或等于10(3)的标本在两种测定法中均呈阳性。毒素A和B ELISA的特异性分别为98.6%和100%。两种毒素的ELISA可替代组织培养细胞毒性测定法。