Abstract |
The gene for feline herpesvirus type 1 (FHV-1) glycoprotein B (gB) has been cloned into an expression vector, pRVSVneo, containing the long terminal repeat of Rous sarcoma virus and polyadenylation signal of SV40. This expression vector containing FHV-1 gB gene, pRVSVgBneo, was transfected into Crandell feline kidney (CRFK) cells which are susceptible to FHV-1 infection. By indirect immunofluorescence analysis, the expressed gB was recognized with a panel of monoclonal antibodies (MAbs) against FHV-1 gp143/108. Immunoprecipitation analysis using a MAb 34H12 showed that molecular weights of the gB were 143 and 108 kDa under non-denaturing conditions that 108, 70, 64, and 58 kDa under denaturing conditions. The molecular weights were similar to those of the gB expressed in FHV-1-infected CRFK cells. In addition, when plasmid DNAs were injected into mice to obtain gB-monospecific serum, the pooled serum from mice inoculated with pRVSVgBneo, but not with pRVSVgDneo or pRVSVneo, recognized the FHV-1 gB polypeptides.
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Authors | K Maeda, K Hirasawa, Y Kawaguchi, M Ono, T Mori, T Gemma, N Yokoyama, K Doi, T Mikami |
Journal | Virus research
(Virus Res)
Vol. 39
Issue 1
Pg. 55-61
(Nov 1995)
ISSN: 0168-1702 [Print] Netherlands |
PMID | 8607284
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Monoclonal
- Antibodies, Viral
- Recombinant Proteins
- Viral Envelope Proteins
- glycoprotein B, Felid herpesvirus 1
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Topics |
- Animals
- Antibodies, Monoclonal
(immunology)
- Antibodies, Viral
(biosynthesis)
- Cats
- Cells, Cultured
- Cloning, Molecular
- Gene Expression
- Genes, Viral
- Genetic Vectors
- Herpesviridae
(genetics)
- Mice
- Mice, Inbred BALB C
- Molecular Weight
- Recombinant Proteins
(biosynthesis, immunology)
- Transfection
(methods)
- Vaccination
- Viral Envelope Proteins
(biosynthesis, genetics, immunology)
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