Bibliography: pages 134-149.Enzyme-linked immunosorbent assay (ELISA) was used successfully to detect cauliflower mosaic virus (CaMV) in crude leaf extracts. Small serological differences between CaMV isolates could be shown by ELISA and serum cross-absorption. Serological reactivity of CaMV was found to depend on the proteolytic degradation state of the virus coat protein so making it impossible to establish definite serological relationships among the virus isolates tested. Proteolysis during purification of CaMV could not be entirely eliminated. The coat protein of CaMV was shown to be glycosylated by the specific binding of labelled Concanavalin A. The role of carbohydrate residues in CaMV serological reactivity was evaluated
To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.