Roeder P L, Le Blanc Smith P M
Australian Animal Health Laboratory, Geelong, Victoria.
Res Vet Sci. 1987 Sep;43(2):225-32.
A highly sensitive indirect sandwich enzyme-linked immunosorbent assay suitable for adoption as the routine diagnostic and typing test for foot-and-mouth disease virus of all seven serotypes is described. The assay uses rabbit and guinea pig antisera raised against inactivated 146S virus antigens. Strong homotypic and minimal heterotypic reactions with both whole virion 146S and derived virion subunit 12S antigens achieved a detection sensitivity approximately 125 times that of the complement fixation test. When applied to diagnostic material with positive-negative threshold criteria generated from testing a large number of negative samples, a positive result was obtained on 83.3 per cent of original virus-positive epithelia, three times the rate for the complement fixation test, and all were typed after one passage in culture.
本文描述了一种高度灵敏的间接夹心酶联免疫吸附测定法,适用于作为所有七种血清型口蹄疫病毒的常规诊断和分型检测。该测定法使用针对灭活的146S病毒抗原产生的兔和豚鼠抗血清。与完整病毒粒子146S和衍生的病毒粒子亚基12S抗原均产生强烈的同型反应和最小的异型反应,检测灵敏度约为补体结合试验的125倍。当将其应用于根据大量阴性样品检测产生的阳性-阴性阈值标准的诊断材料时,在83.3%的原始病毒阳性上皮细胞上获得了阳性结果,是补体结合试验阳性率的三倍,并且所有样品在培养传代一次后均进行了分型。