Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9604378 | Journal of Biotechnology | 2005 | 10 Pages |
Abstract
The VP60 capsid protein from rabbit hemorrhagic disease virus (RHDV) (Spanish isolate AST/89) was cloned and expressed in Pichia pastoris. The transformed yeast was grown at high cell density and an expression level of about 1.5 g VP60 Lâ1 culture was obtained. The protein was detected associated with the cell debris fraction of the recombinant yeast after mechanical disruption. It was purified by a simple method and was obtained N-glycosylated with purity of approximately 70% as deduced from densitometry scan analysis. The recombinant product was antigenically similar to the native capsid protein as determined with polyclonal antibodies obtained from rabbits vaccinated with VP60 protein purified from native virus. The immunogenicity of VP60 protein purified from P. pastoris was demonstrated by ELISA in a vaccination experiment conducted with two groups of rabbits subcutaneously immunized. Animals vaccinated with VP60 in Freund's incomplete adjuvant developed a significant (p < 0.01) virus-specific antibody response while the group injected with placebo remained seronegative. Preliminary results showed that the antigen administered within the cell debris fraction of the transformed yeast protected rabbits immunized by the oral route against an intramuscular challenge with 100 LD50 (16,000 hemagglutination units) of homologous virus.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Omar Farnós, Oscar Boué, Francisco Parra, José Manuel MartÃn-Alonso, Odaysa Valdés, Marisdania Joglar, Leonor Navea, Paula Naranjo, Ricardo Lleonart,