A SINGLE DILUTION ENZYME-LINKED IMMUNOSORBENT-ASSAY FOR THE QUANTITATIVE DETECTION OF ANTIBODIES TO BOVINE HERPESVIRUS TYPE-1

Three serological assays were compared for detection of antibodies to bovine herpes virus type 1. These were virus neutralization (VN), enhanced complement fixation (CF) and ELISA. The ELISA was developed using an infected cell lysate antigen and purified virus and was optimized in relation to antigen and antisera dilutions. The CF assay was enhanced by the addition of bovine complement. These 3 assays were compared for detection of: specific virus antibody titers; sero-conversions; early antibody response in experimentally-infected cattle. ELISA end-point titers and single dilution values were more sensitive than the CF or VN assays for specific antibody level quantitation. With a single dilution ELISA test procedure a correlation was obtained between ELISA values and VN titers. Using the single dilution ELISA test the assay also detected antibodies in experimentally infected cattle before either the VN or CF assays, and agreed with the VN test in 35/38 seroconversions found by .gtoreq. 4-fold VN changes between acute and convalescent paired sera from naturally-infected animals. The single dilution ELISA was a rapid and sensitive test for routine antibody detection in bovine sera.