Presentation of subunit vaccines in a highly ordered aggregate form ca
n result in enhanced immune responses. Coat protein (CP) monomers of a
potyvirus (Johnsongrass mosaic virus) when produced in heterologous h
ost expression systems (Escherichia coli, yeast and insect cells) self
-polymerized to produce potyvirus-like particles (PVLPs). The N- and C
-terminal regions of potyvirus CP are surface-exposed and are not requ
ired for assembly. Hybrid CP monomers containing short peptides fused
to their N- and/or C-termini, or large target antigens fused to the N-
terminus or replacing most of the N- or C-terminal exposed regions ret
ained the ability to assemble into hybrid PVLPs. Such chimeric PVLPs w
ere highly immunogenic in mice and rabbits even in the absence of any
adjuvant. Potyvirus CP is highly versatile in accommodating peptides o
r large antigens and is able to present antigens exposed on the surfac
e of virus-like particles. This, combined with the efficiency of high
level bacterial and insect cell expression systems, makes PVLPs an att
ractive non-pathogenic and non-replicative vaccine carrier.