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Monospecific ssra against protein subunlts of bovine adenovirus (BAV) types 2» 3 and 7 were produced in rabbits, using agarose immunopreeipitates prepared by preparative Immunoelectrophoresis, Various forms o( solubillxed viral antigens were separated in line or crossed Immunoelectrophoresis using type-specific hyperimmune sera. The specifi­ cities of these sera were determined by icmunoprecipitation/sodium dodecylsulfate polyacrylamide gel electrophoreaia (IP/SOS PAGE)» Western blot and immunodiffusion. The viral neutralization potentials of these sera were analyzed using in vitro tests in homologous and heterologous systems. Since both viral neutralizing and non-neutralizing mono­ specific sera to hexons were obtained, a peptide mapping system using limited proteolysis in SOS PACE was employed to detect any differences that may be present in the hexon polypeptides precipitated in IP/SOS PACE. In addition, BAV-3 hexon subunlts, produced by deoxycholate and heat treatment followed by DEAE BioCel A chromatography, were used to produce hyperimmune sera. These anei-hexon sera seemed to be superior to the monospecific sera produced from agarose inmunoprecipitates in that they possessed subgroup-reactive neutralizing activities in addition to type-reactive ones. The presence of hexon subunlts capable of inducing both subgroupand type-specific viral neutralizing antibodies makes this subunit preparation an ideal candidate for use in a multivalent subunit vaccine.

Isolation and evaluation of the immunizing subunits of bovine adenovirus types 2, 3 and 7