Source:http://linkedlifedata.com/resource/pubmed/id/16216377
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2006-2-14
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pubmed:databankReference | |
pubmed:abstractText |
Cytopathogenic (cp) bovine viral diarrhea virus (BVDV) strain KS86-1 cp was isolated from a cow persistently infected with non-cytopathogenic (ncp) BVDV strain KS86-ncp after development of mucosal disease by superinfection with cp BVDV strain Nose. cp BVDV strains 799cp and 839cp were also isolated from independent cattle that developed mucosal disease by superinfection with cp BVDV KS86-1cp. In the present study, genetic analysis revealed that the genes of cp BVDV strains 799cp and 839cp were chimeras between the genes of the persisting ncp BVDVs and that of superinfecting KS86-1cp. The genetic recombination that generates 799cp occurred between the identical points in the N(pro) gene region, whereas genetic recombination that generates 839cp occurred between different points in the N(pro) gene region. Both 799cp and 839cp were inherited Jiv gene of KS86-1cp strain and envelope protein genes of the persisting viruses. In addition, neutralization test disclosed that antigenicities of 799cp, 839cp, and KS86-1cp were also similar to each persisting virus. These findings indicate that exogenous cp BVDV containing insertion of Jiv gene in the 5 terminal region can induce genetic recombination with the original ncp BVDV at different points in the N(pro) gene region, and those viruses have high potential to change those antigenicities and pathogenicities by RNA recombination.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Npro protein, bovine viral...,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Envelope Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0168-1702
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
116
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
78-84
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16216377-Animals,
pubmed-meshheading:16216377-Antibodies, Viral,
pubmed-meshheading:16216377-Antigens, Viral,
pubmed-meshheading:16216377-Cattle,
pubmed-meshheading:16216377-Cells, Cultured,
pubmed-meshheading:16216377-Cross Reactions,
pubmed-meshheading:16216377-Diarrhea Viruses, Bovine Viral,
pubmed-meshheading:16216377-Genome, Viral,
pubmed-meshheading:16216377-Molecular Sequence Data,
pubmed-meshheading:16216377-Neutralization Tests,
pubmed-meshheading:16216377-Nucleic Acid Amplification Techniques,
pubmed-meshheading:16216377-RNA, Viral,
pubmed-meshheading:16216377-Recombination, Genetic,
pubmed-meshheading:16216377-Sequence Analysis, DNA,
pubmed-meshheading:16216377-Viral Envelope Proteins,
pubmed-meshheading:16216377-Viral Proteins
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pubmed:year |
2006
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pubmed:articleTitle |
Genetic recombination at different points in the Npro-coding region of bovine viral diarrhea viruses and the potentials to change their antigenicities and pathogenicities.
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pubmed:affiliation |
Laboratory of Microbiology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Kita 18 Nishi 9, Sapporo 060-0818, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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