Lunt R A, White J R, Della-Porta A J
CSIRO, Australian Animal Health Laboratory, Geelong, Vic.
Vet Microbiol. 1988 Apr;16(4):323-38. doi: 10.1016/0378-1135(88)90014-4.
An ELISA for the detection of serum antibody in sheep, cattle and goats to the viruses of bluetongue (BTV) and epizootic haemorrhagic disease of deer (EHDV) has been developed. Two methods of antigen preparation were analysed for efficacy in the ELISA and inter-group seroreactivity. A freeze-thaw (F/T) antigen appeared to have a narrower specificity than a cytoskeletal preparation from infected cells (P200) which contained all viral proteins. A higher background reactivity was seen when using the P200 antigen, suggesting that a F/T antigen, perhaps as a composite of serotypes, would be of greater value in an ELISA to replace current methods for antibody screening. The effect of multiple infections with unrelated orbiviruses was found to have no effect on the detection of antibody to BTV and EHDV by ELISA. The ELISA was able to demonstrate development and persistence of antibody to BTV in cattle over the course of 120 days.
已开发出一种酶联免疫吸附测定法(ELISA),用于检测绵羊、牛和山羊血清中针对蓝舌病病毒(BTV)和鹿流行性出血病病毒(EHDV)的抗体。分析了两种抗原制备方法在ELISA中的效果以及组间血清反应性。冻融(F/T)抗原的特异性似乎比来自感染细胞的细胞骨架制剂(P200,其中包含所有病毒蛋白)更窄。使用P200抗原时观察到更高的背景反应性,这表明F/T抗原,也许作为血清型的复合物,在ELISA中替代当前抗体筛查方法可能具有更大价值。发现感染无关环状病毒对通过ELISA检测针对BTV和EHDV的抗体没有影响。该ELISA能够证明牛在120天内针对BTV抗体的产生和持续存在。