| Project/Area Number |
01860041
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| Research Category |
Grant-in-Aid for Developmental Scientific Research
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| Allocation Type | Single-year Grants |
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| Research Field |
Applied veterinary science
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| Research Institution | The university of Tokyo |
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Principal Investigator |
MIKAMI Takeshi Univ. of Tokyo, Fac. of Agr., Professor, 農学部, 教授 (20091506)
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| Co-Investigator(Kenkyū-buntansha) |
OKAZAKI Katsunori Tokyo Univ. of Agr. and Tec. Fac. of Agr. Research Associate, 農学部, 助手 (90160663)
NAKAJIMA Kazuhiro Natl. Res. Inst. of Aquaculture, Fisheries Agency, 養殖研究所, 研究員 (60207777)
MATSUDA Haruo Hiroshima Univ. Fac. of Appl. Biolog. Sci. Assoc. Prof., 生物生産学部, 助教授 (80116863)
HIRAI Kanji Tokyo Med. and Dent. Univ. Professor, 医学部, 教授 (00100991)
TAKAHASHI Eiji Univ. of Tokyo, Fac. of Agr., Professor, 農学部, 教授 (50183439)
東原 朋子 帝京大学, 医学部, 助手 (90173145)
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| Project Period (FY) |
1989 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥17,700,000 (Direct Cost: ¥17,700,000)
Fiscal Year 1991: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1990: ¥7,100,000 (Direct Cost: ¥7,100,000)
Fiscal Year 1989: ¥9,100,000 (Direct Cost: ¥9,100,000)
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| Keywords | very virulent Marek's disease virus / vaccine / Marek's disease / CD4-depleted chicken / CD-8depleted chicken / mechanism of vaccine protection / mechanism of tumorigenesis / preventive measure / マレック病ウイルスA抗原 / マレック病ウイルスB抗原 / バキュロウイルス / リコンビナントウイルス / 起強毒マレック病ウイルス / ワクチンブレイク / 遺伝子構造 / 単クロ-ン性抗体 |
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| Research Abstract |
For prevention of Marek's disease (MD) caused by Marek's disease virus (MDV), monovalent vaccine of herpesvirus of turkey has been widely used for chickens in the field. Recently, however, MD caused by very virulent MDV (vvMDV) was observed in vaccinated chicknes. The final aim of the present study is to develop MD vaccine such as recombiant, polyvalent or component vaccine for controlling the outbreak of MD due to vvMDV. The following results were obtained.
1) Arecombinant baculovirus expressing the A antigen (rBV-A) of MDV was constructed. In Spodoptera frugiperda (Sf) cells infectedwith the rBV-A, A antigen (A Ag) expression was localized to the cell surface. By immunoprecipitation of ^<35>S labelled A Ag with a monoclonal antibody to A Ag, a large amount of the A Ag(58-68kDa) was dtected of the rBV-A infected cells but a small amount of the antigen (46-54kDa) was found in the culture supenatant of infected cells. The reconminant A Ag was shown to be reactive with sera of MDV-infected chickens. In sera of chickens immunized with the A Ag, MDV-specific antibody reactive with MDV-infected cells was found.
2) A gene encoding a homolog of glycoprotein B of herpes simplex virus (gB homolog) has been identified on the MDV genome. The recombinant baculovirus encoding the gB homolog (rBV-B) of MDV expressed the protein in the cytoplasm and on the surface of Sf cells infected with the rBV-B, when examined by immunofluorescent assay using anti-B sera from chickens or rabbits, and monoclonal antibody against B antigen. The expressed protein had three molecular sized (88/100, 64 and 54kDa).
3) Chicks thymectomized and injected with either monoclonal antibody to chicken CD4 of CD8 were infected with vvMDV. The CD8-depleed chcks developed both nerve enlargement and visceral tumor, whereas the CD4-depleted chicks showed only nerve enlargement.
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