Abstract
Mouse monoclonal antibodies (McAbs) for cryptotopes or neotopes of tulip breaking polyvirus (TBV) were selected on antigen-coated plates. These antigenic determinants were apparently selected because of the instability of the virus in the alkaline condition. Cryptotopes are exposed when the virus is degraded, and neotopes are created due to novel antigenic specificities under a particular environment. In double-antibody sandwich enzyme-linked immunosorbent assay (DAS ELISA), lower A405 readings were obtained with TBV McAb-coated than with TBV polyclonal antibody (PAb)-coated plates. In ELISA on antigen-coated plates, detection of purified TBV was more sensitive with enzyme-labeled McAbs than with enzyme-labeled PAbs. In plates coated with TBV-infected saps, a higher A405 reading was obtained with enzyme-labeled PAbs than with enzyme-labeled McAbs. Tulip breaking virus McAbs could be used to differentiate strains of TBV, and some also reacted to bean yellow mosaic polyvirus. One McAb also reacted to iris severe mosaic polyvirus. None of the McAbs reacted to lily symptomless carlavirus or lily potexvirus X.