대한바이러스학회지 (The Journal of Korean Society of Virology)
- 제26권2호
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- Pages.163-171
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- 1996
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- 1225-2344(pISSN)
Baculovirus Vector System에 의해 발현된 재조합 Pseudorabies Virus Major Capsid Protein의 면역원성
Immunogenicity of the Recombinant Pseudorabies Virus Major Capsid Protein Expressed by Baculovirus Vector System
- 전무형 (충남대학교 수의과대학) ;
- 안동준 (수의과학연구소) ;
- 장경수 (충남대학교 수의과대학) ;
- 조용성 (충남대학교 수의과대학) ;
- 박종현 (수의과학연구소) ;
- 송재영 (수의과학연구소) ;
- 현방훈 (수의과학연구소) ;
- 안수환 (수의과학연구소)
- Jun, Moo-Hyung (College of Veterinary Medicine, Chungnam National University) ;
- An, Dong-Jun (Veterinary Research Institute) ;
- Chang, Kyung-Soo (College of Veterinary Medicine, Chungnam National University) ;
- Cho, Young-Sung (College of Veterinary Medicine, Chungnam National University) ;
- Park, Jong-Hyeon (Veterinary Research Institute) ;
- Song, Jae-Young (Veterinary Research Institute) ;
- Hyun, Bang-Hun (Veterinary Research Institute) ;
- An, Soo-Hwan (Veterinary Research Institute)
- 발행 : 1996.12.30
초록
The recombinant pseudorabies virus major capsid protein (rMCP) was produced by expression of the MCP gene in Sf-9 cell using baculovirus transfer vector system. Following evaluation of the immunochemical properties of the rMCP, the immunogenicity of the recombinant subunit protiens were investigated in guinea pig and swine to obtain the preliminary guide line for the subunit vaccine using rMCP and gP50. It was proved that ultrasonication and 30% ammonium sulfate was most efficient to concentrate and purify the protein. The rMCP was safe in mice, guinea pigs and piglets. In guinea pigs, rMCP mixed with various adjuvants induced substantial degree of serum neutralizing antibody titers, but revealed incomplete protectivity against challenge. In swine, the combination of rMCP and gP50 showed the higher serum neutralizing antibody titers and cellular immune responses than rMCP alone. However, the protectivity was lower in comparison with the commercial gI-deleted inactivated vaccine. We expect these results to contribute to characterization of MCP gene of Korean isolate of PRV and to ultilize as preliminary information for prodution and evaluation of PRV recombinant subunit vaccines.
키워드