C. Porta et al., DEVELOPMENT OF COWPEA MOSAIC-VIRUS AS A HIGH-YIELDING SYSTEM FOR THE PRESENTATION OF FOREIGN PEPTIDES, Virology, 202(2), 1994, pp. 949-955
It has recently been shown that cowpea plants can be infected with a c
owpea mosaic virus (CPMV) chimera containing an antigenic site from fo
ot-and-mouth disease virus (Usha et al., Virology 197, 366-374, 1993).
Analysis of progeny RNA produced during such an infection has reveale
d that the inserted sequence is rapidly lost during serial passaging,
probably by a process of homologous recombination. Using the informati
on gained from this analysis, we have redesigned the chimeras in such
a way that they are now genetically stable. The modified constructs ha
ve been used to obtain large quantities of purified virus particles ex
pressing epitopes derived from human rhinovirus 14 (HRV-14) and human
immunodeficiency virus type 1 (HIV-1). The chimeric virus particles po
ssess the antigenic properties of the inserted sequence and, in the ca
se of the HRV-14-derived construct, it has been shown that the inserte
d epitope is immunogenic in rabbits. These results demonstrate that CP
MV can be used as a high-yielding system for the presentation of forei
gn peptide sequences. (C) 1994 Academic Press, Inc.