Abstract
Successful field oral vaccination and protection against viral diseases have so far been achieved only with live-attenuated or live-recombinant virus vaccines. In this communication, we present data that demonstrate that a glycoprotein derived from recombinant baculovirus-infected insect cells is efficacious as an oral vaccine. The glycoprotein (G) of rabies virus (Evelyn Rokitnicki Abelseth strain) was abundantly expressed in a baculovirus expression system and oral vaccination of racoons with the baculovirus-expressed G protein resulted in the production of rabies virus-neutralizing antibodies and protection against a lethal challenge with a street rabies virus. The potential for using the baculovirus-expressed G protein for oral immunization of wildlife is discussed.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Administration, Oral
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Animals
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Antibodies, Viral / biosynthesis*
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Antibodies, Viral / immunology
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Antigens, Viral*
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Baculoviridae*
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Cells, Cultured
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Cricetinae
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Glycoproteins / administration & dosage
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Glycoproteins / immunology*
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Kidney
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Mesocricetus
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Moths
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Rabies / prevention & control
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Rabies Vaccines / administration & dosage*
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Rabies Vaccines / immunology
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Rabies virus / immunology*
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Raccoons / immunology*
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Recombinant Fusion Proteins / immunology
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Vaccination / methods
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Vaccination / veterinary*
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Vaccines, Synthetic / administration & dosage*
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Vaccines, Synthetic / immunology
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Viral Envelope Proteins / administration & dosage
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Viral Envelope Proteins / immunology*
Substances
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Antibodies, Viral
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Antigens, Viral
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Glycoproteins
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Rabies Vaccines
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Recombinant Fusion Proteins
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Vaccines, Synthetic
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Viral Envelope Proteins
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glycoprotein G, Rabies virus