Abstract
Two recombinant adenoviruses were constructed expressing foot-and-mouth disease virus (FMDV) capsid and 3C/3CD proteins in replicative deficient human adenovirus type 5 vector. Guinea pigs vaccinated with 1-3 x 10(8)TCID(50) Ad-P12x3C recombinant adenovirus were completely protected against 10,000GID(50) homologous virulent FMDV challenge 25 days post vaccination (dpv). Ad-P12x3CD vaccinated guinea pigs were only partially protected. Swine were vaccinated once with 1x10(9)TCID(50) Ad-P12x3C hybrid virus and challenged 28 days later. Three of four vaccinated swine were completely protected against 200 pig 50% infectious doses (ID(50)) of homologous FMDV challenge, and vaccinated pigs developed specific cellular and humoral immune responses. The immune effect of Ad-P12x3C in swine further indicated that the recombinant adenovirus was highly efficient in transferring the foreign gene. This approach may thus be a very hopeful tool for developing FMD live virus vector vaccine.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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3C Viral Proteases
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Adenoviridae* / genetics
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Animals
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Antibodies, Viral / blood
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Capsid* / immunology
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Capsid* / metabolism
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Cysteine Endopeptidases* / genetics
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Cysteine Endopeptidases* / immunology
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Cysteine Endopeptidases* / metabolism
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Foot-and-Mouth Disease / immunology
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Foot-and-Mouth Disease / prevention & control*
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Foot-and-Mouth Disease / virology
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Foot-and-Mouth Disease Virus / classification
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Foot-and-Mouth Disease Virus / immunology*
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Guinea Pigs
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Recombinant Proteins* / administration & dosage
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Recombinant Proteins* / immunology
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Recombinant Proteins* / metabolism
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Serotyping
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Swine
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Swine Diseases / immunology
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Swine Diseases / prevention & control*
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Swine Diseases / virology
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Vaccination / veterinary
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Viral Proteins* / genetics
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Viral Proteins* / immunology
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Viral Proteins* / metabolism
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Viral Vaccines / administration & dosage
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Viral Vaccines / immunology
Substances
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Antibodies, Viral
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Recombinant Proteins
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Viral Proteins
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Viral Vaccines
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Cysteine Endopeptidases
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3C Viral Proteases