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Volume 65,
Issue 12,
1984
Volume 65, Issue 12, 1984
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Biochemical and Serological Studies of Pathogenesis-related Proteins of Nicotiana Species
More LessSUMMARYPathogenesis-related proteins (PR proteins), found in leaves of different Nicotiana spp. infected with tobacco mosaic virus (TMV) or treated with potassium salicylate, were compared biochemically and also serologically using an antibody to PR1a purified from TMV-infected leaves of Nicotiana tabacum cv. Samsun NN. The antibody preparation reacted with PR proteins, PR1a, PR1b and PR1c, from four cultivars of N. tabacum and with a PR protein, b1″, from TMV-infected leaves of Nicotiana glutinosa, but not with a PR protein, PR2, from cv. Samsun NN. The isoelectric points in 9 m-urea of PR1a and PR1b from N. tabacum cv. Samsun NN were pH 4.3 and 4.8, respectively. Partial proteolysis of PR1a and PR1b with Pronase E yielded peptides which, although similar in size to those from PR1b, differed from them serologically. When Staphylococcus aureus V8 protease was used, the peptides released from each protein differed both in size and serological reaction. The patterns of peptides released from b1″ of N. glutinosa by V8 protease and Pronase E were different from those of peptides from PR1a and PR1b from N. tabacum. The antibody preparation reacted strongly with one of four peptides released by Pronase E and with two of the three peptides released by V8 protease. These results indicate that PR1a, PR1b and PR1c from N. tabacum and b1″ from N. glutinosa contain some similar antigenic determinants and have similar structures, and confirm that PR1a and PR1b are very similar but not identical in their primary structures.
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Distribution of Barley Stripe Mosaic Virus Protein in Infected Wheat Root and Shoot Tips
More LessSUMMARYPost-sectioning immunogold—silver staining (IGSS) specifically detected barley stripe mosaic virus (BSMV) protein in Lowicryl- or Araldite-embedded plant tissues at the light microscope level. Electron microscopy of adjacent sections showed that BSMV particles were present where the IGSS reaction was positive. BSMV protein was localized in or near the apical meristems of root and shoot tips of systemically infected wheat. Infected cells were distributed in a mosaic pattern.
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Serological Studies of Dianthoviruses Using Monoclonal and Polyclonal Antibodies
More LessSUMMARYIn comparative serological studies of dianthoviruses, reverse passive haemagglutination inhibition (RPHI) tests distinguished between sweet clover necrotic mosaic virus (SCNMV) and each of a Swedish isolate of red clover necrotic mosaic virus (RCNMV-SW), the clover primary leaf necrosis strain of RCNMV (RCNMV-C) and carnation ringspot virus (CRSV). Twenty-one monoclonal antibodies prepared against SCNMV were highly specific and failed to react with RCNMV-SW, RCNMV-C or CRSV when tested by RPHI. The extent of the differences between these dianthoviruses was assessed by direct ELISA using polyclonal antibodies. No heterologous reaction was detected by direct ELISA, but indirect ELISA revealed a distant serological relationship between CRSV and each of the other viruses. This is the first report of a positive serological relationship between CRSV and other dianthoviruses.
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