Bishai F R, Spence L, Goodwin D, Petro R
Can J Microbiol. 1979 Sep;25(9):1118-24. doi: 10.1139/m79-174.
Two ELISA systems for the detection of human rotaviruses were developed. In the first system antibodies to Nebraska calf diarrhea virus (NCDV) were used for coating the solid matrix and for the preparation of the enzyme conjugate. In the second system antibodies to human rotavirus and antibodies to simian rotavirus (SA11) were used for coating the solid matrix and for the preparation of the enzyme conjugate respectively. The second ELISA system proved to have a broader spectrum for the detection of human rotaviruses. By using the two ELISA systems, the different types of human rotavirus could be distinguished. The ELISA tests developed were 8 to 64 times as sensitive as electron microscopy (EM) and (or) counterimmunoelectrophoresis (CIEP). The antigen detected by ELISA was shown to be different from that detected by the hemagglutination test.
开发了两种用于检测人类轮状病毒的酶联免疫吸附测定(ELISA)系统。在第一种系统中,使用抗内布拉斯加小牛腹泻病毒(NCDV)的抗体包被固相基质并制备酶结合物。在第二种系统中,分别使用抗人类轮状病毒的抗体和抗猴轮状病毒(SA11)的抗体包被固相基质并制备酶结合物。事实证明,第二种ELISA系统在检测人类轮状病毒方面具有更广泛的谱。通过使用这两种ELISA系统,可以区分不同类型的人类轮状病毒。所开发的ELISA试验的灵敏度是电子显微镜(EM)和(或)对流免疫电泳(CIEP)的8至64倍。ELISA检测到的抗原显示与血凝试验检测到的抗原不同。