Jy. Ho et al., Expression, purification, and characterization of the infectious bursal disease virus-like particles produced by insect cells, J CHIN CHEM, 46(5), 1999, pp. 743-750
The cDNA of the large genomic segment A (ORF A1) of infectious bursal disea
se virus (IBDV) strain P3009 was synthesized and cloned into the transfer v
ector pBlueBac4. Following cotransfection and plaque purification, a plaque
-pure recombinant baculovirus, vIBDVJ6, was selected to express IBDV capsid
proteins. When Sf9 cells were infected with vIBDVJ6, IBDV precursor protei
n (polypeptide of VP2-VR4-VP3) was expressed and proteolytically processed
to give VP2, VP3, and VP4 proteins by a viral protease. These resulting rec
ombinant proteins can self-assemble to form virus-like particles (VLPs). Th
e shape and size of the negatively stained purified IBDV-like particles wer
e demonstrated to be similar to those of the complete P3009 IBDV particles
under direct electron microscopic observation. Furthermore, the purified pa
rticles were strongly recognized by an anti-VP2 monoclonal antibody as conf
irmed by an immune-gold labeling experiment. IBDV-like particles will offer
a unique opportunity to create completely non-infectious viral vaccines fo
r use in the vaccination of chickens. The immunologic response in chickens
stimulated by IBDV-like particles is currently being evaluated.