An indirect enzyme-linked immunosorbent assay (ELISA) for the diagnosis of bovine leukaemia virus (BLV) infection was developed and compared with the agar gel immunodiffusion test (ACID?. Western blotting (WB) was used as confirmatory test. ELISA and AGIDT had specificities that were comparable with that of WB, however, ELSA showed a higher sensitivity than AGIDT. The ELISA was useful for screening a large number of samples, whereas WB was important for detecting the antibody response against the individual BLV-proteins. Different types of positive serological reactions were discerned in m, that correlated with reactions of sera in AGIDT and ELISA. The most important antigen in WB and
E~S Awas the BLV protein p24, whereas the BLV glycoproteins gp51 and gp30 were o f special importance in AGIDT. The relevance of repeatedly testing the antibody response in BLV-infected herds for control 2nd eradication programmes using assays with higher sensiuvity than AGIDT was demonstrated.