Source:http://linkedlifedata.com/resource/pubmed/id/10580045
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1999-12-15
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pubmed:databankReference | |
pubmed:abstractText |
Expression cassettes containing the codons for the pestivirus E (rns) signal peptide (Sig) followed by a chemically synthesized ORF that encoded the bovine viral diarrhoea virus (BVDV) strain C86 glycoprotein E2, a class I membrane glycoprotein, were constructed with and without a chimeric intron sequence immediately upstream of the translation start codon, and incorporated into the genome of bovine herpesvirus-1 (BHV-1). The resulting recombinants, BHV- 1/SigE2(syn) and BHV-1/SigE2(syn)-intron, expressed comparable quantities of glycoprotein E2, and Northern blot hybridizations indicated that the presence of the intron did not increase significantly the steady-state levels of transcripts encompassing the SigE2(syn) ORF. In BHV-1/SigE2(syn)- infected cells, the 54 kDa E2 glycoprotein formed a dimer with an apparent molecular mass of 94 kDa, which was further modified to a 101 kDa form found in the envelope of recombinant virus particles. Penetration kinetics and single-step growth curves indicated that the incorporation of the BVDV E2 glycoprotein in the BHV-1 envelope, which apparently did not require BHV-1-specific signals, interfered with entry into target cells and egress of progeny virions. These results demonstrate that a pestivirus glycoprotein can be expressed efficiently by BHV-1 and incorporated into the viral envelope. BHV-1 thus represents a promising tool for the development of efficacious live and inactivated BHV-1-based vector vaccines.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0022-1317
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
80 ( Pt 11)
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2839-48
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10580045-Amino Acid Sequence,
pubmed-meshheading:10580045-Animals,
pubmed-meshheading:10580045-Base Sequence,
pubmed-meshheading:10580045-Cattle,
pubmed-meshheading:10580045-Cells, Cultured,
pubmed-meshheading:10580045-Diarrhea Viruses, Bovine Viral,
pubmed-meshheading:10580045-Herpesvirus 1, Bovine,
pubmed-meshheading:10580045-Introns,
pubmed-meshheading:10580045-Molecular Sequence Data,
pubmed-meshheading:10580045-Open Reading Frames,
pubmed-meshheading:10580045-Recombinant Proteins,
pubmed-meshheading:10580045-Transcription, Genetic,
pubmed-meshheading:10580045-Viral Envelope Proteins,
pubmed-meshheading:10580045-Virion
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pubmed:year |
1999
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pubmed:articleTitle |
Expression of bovine viral diarrhoea virus glycoprotein E2 by bovine herpesvirus-1 from a synthetic ORF and incorporation of E2 into recombinant virions.
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pubmed:affiliation |
Institute of Molecular Biology, Friedrich-Loeffler-Institutes, Federal Research Centre for Virus Diseases of Animals, D-17498 Insel Riems, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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