Identification of B-cell epitopes on the betanodavirus capsid protein

The pepscan procedure was used to identify betanodavirus B-cell epitopes recognized by neutralizing mouse monoclonal antibodies (MAbs) and serum samples obtained from sea bass, Dicentrarchus labrax, naturally infected with betanodavirus. Pepscan was performed with a panel of thirty-four 12-mer synth...

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Détails bibliographiques
Publié dans:Journal of fish diseases. - 1998. - 30(2007), 7 vom: 15. Juli, Seite 419-26
Auteur principal: Costa, J Z (Auteur)
Autres auteurs: Adams, A, Bron, J E, Thompson, K D, Starkey, W G, Richards, R H
Format: Article
Langue:English
Publié: 2007
Accès à la collection:Journal of fish diseases
Sujets:Journal Article Research Support, Non-U.S. Gov't Antibodies, Monoclonal Capsid Proteins Epitopes, B-Lymphocyte
Description
Résumé:The pepscan procedure was used to identify betanodavirus B-cell epitopes recognized by neutralizing mouse monoclonal antibodies (MAbs) and serum samples obtained from sea bass, Dicentrarchus labrax, naturally infected with betanodavirus. Pepscan was performed with a panel of thirty-four 12-mer synthetic peptides that mimicked the entire betanodavirus capsid protein. Sea bass serum samples reacted strongly with three regions of the capsid protein comprising amino acid residues 1-32, 91-162 and 181-212. The latter region was also recognized by neutralizing MAbs and coincided with a region of high antigenic propensity identified by an antigen prediction algorithm. These data suggest that a region of the betanodavirus capsid protein spanning amino acid residues 181-212 may represent a neutralization domain that could potentially be used to inform the development of nodavirus vaccines and immunodiagnostic reagents
Description:Date Completed 28.09.2007
Date Revised 30.09.2020
published: Print
Citation Status MEDLINE
ISSN:1365-2761