Abstract
Vaccinia virus (VV) was successfully used as a live vaccine to eradicate smallpox, but the nature of viral proteins involved in eliciting viral immunity has not yet been identified. A potential candidate is a 14-kDa VV envelope protein that is involved in virus penetration at the level of virus-cell fusion, in cell-cell fusion late in infection, and in virus dissemination. The 14-kDa envelope protein has been produced in Escherichia coli, with properties similar to those of the native protein found in the virus particle and in infected cells (C. Lai, S. Gong, and M. Esteban, J. Biol. Chem. 256:22174-22180, 1990). In this investigation, we showed that mice immunized with purified VV 14-kDa protein synthesized in E. coli in the form of a monomer or a trimer develop high-titer neutralizing antibodies and are protected when challenged with lethal doses of wild-type VV. Our findings demonstrate that it is possible to confer protection against VV through immunization with the 14-kDa envelope protein.
MeSH Terms
Ammonium Sulfate
Animals
Antibodies, Viral/analysis
Antibody Formation
Chromatography
Chromatography, Gel
Chromatography, Ion Exchange
Cloning, Molecular/methods
Durapatite
Escherichia coli/genetics
Hydroxyapatites
Immunization
Mice
Mice, Inbred BALB C
Molecular Weight
Recombinant Proteins/immunology,isolation & purification
Vaccinia/immunology
Vaccinia virus/genetics,immunology
Viral Envelope Proteins/genetics,immunology,isolation & purification
Chemicals
Antibodies, Viral
Hydroxyapatites
Recombinant Proteins
Viral Envelope Proteins
Durapatite
Ammonium Sulfate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lai C F
Department of Biochemistry, State University of New York, Brooklyn 11203.
Gong S C
Esteban M
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