A synthetic peptide corresponding to bovine rotavirus C486 (BRV) VP4 a
mino acid sequence 232-255 (VP4-peptide) was studied with the objectiv
e of defining the origin of the protective immune response reported pr
eviously by Ijaz et al. (J. Virol. 1991, 65, 3106-3113). Pretreatment
of MA-104 cells with the VP4-peptide before infection with rotavirus,
prevented both the attachment of S-35-labelled virus and plaque format
ion in vitro. In vivo studies using a murine rotavirus model demonstra
ted that intragastric administration of VP4-peptide protected subjects
from challenge with virulent rotavirus. These results clearly indicat
e the importance of this epitope in virus-cell interactions and their-
potential as a rotavirus vaccine candidate. (C) 1998 Elsevier Science
Ltd. All rights reserved.