Codon optimization of the rabbit hemorrhagic disease virus (RHDV) capsid gene leads to increased gene expression in Spodoptera frugiperda 9 (Sf9) cells.
10.4142/jvs.2013.14.4.441
- Author:
Jingpeng GAO
1
;
Chunchun MENG
;
Zongyan CHEN
;
Chuanfeng LI
;
Guangqing LIU
Author Information
1. Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai 200241, China. liugq@shvri.ac.cn
- Publication Type:Original Article ; Evaluation Studies ; Research Support, Non-U.S. Gov't
- Keywords:
capsid protein;
codon optimization;
rabbit hemorrhagic disease;
Spodoptera frugiperda 9 cells
- MeSH:
Animals;
Antigens, Viral/genetics/metabolism;
Caliciviridae Infections/prevention & control/*veterinary/virology;
Capsid Proteins/*genetics/metabolism;
Cell Culture Techniques/*methods;
Codon/genetics/metabolism;
Enzyme-Linked Immunosorbent Assay/veterinary;
*Gene Expression Regulation, Viral;
Hemorrhagic Disease Virus, Rabbit/*genetics/immunology;
*Rabbits;
Recombinant Proteins/genetics/metabolism;
Sf9 Cells;
Spodoptera;
Viral Structural Proteins/*genetics/metabolism;
Viral Vaccines/genetics/immunology
- From:Journal of Veterinary Science
2013;14(4):441-447
- CountryRepublic of Korea
- Language:English
-
Abstract:
Rabbit hemorrhagic disease (RHD) is contagious and highly lethal. Commercial vaccines against RHD are produced from the livers of experimentally infected rabbits. Although several groups have reported that recombinant subunit vaccines against rabbit hemorrhagic disease virus (RHDV) are promising, application of the vaccines has been restricted due to high production costs or low yield. In the present study, we performed codon optimization of the capsid gene to increase the number of preference codons and eliminate rare codons in Spodoptera frugiperda 9 (Sf9) cells. The capsid gene was then subcloned into the pFastBac plasmid, and the recombinant baculoviruses were identified with a plaque assay. As expected, expression of the optimized capsid protein was markedly increased in the Sf9 cells, and the recombinant capsid proteins self-assembled into virus-like particles (VLPs) that were released into the cell supernatant. Rabbits inoculated with the supernatant and the purified VLPs were protected against RHDV challenge. A rapid, specific antibody response against RHDV was detected by an ELISA in all of the experimental groups. In conclusion, this strategy of producing a recombinant subunit vaccine antigen can be used to develop a low-cost, insect cell-derived recombinant subunit vaccine against RHDV.
