Source:http://linkedlifedata.com/resource/pubmed/id/15371153
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2004-9-16
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pubmed:databankReference | |
pubmed:abstractText |
Bovine herpesvirus type 5 (BHV-5) is an alphaherpesvirus that causes fatal encephalitis in calves. Envelope glycoproteins E (gE) and gI of alphaherpesviruses are important for the pathogenesis in vivo. Previously the authors determined that BHV-5 gE is important for BHV-5 neurovirulence. To determine the role of gI in BHV-5 neurovirulence, the authors have constructed gI-deleted and gI-revertant BHV-5 and analyzed their neuropathogenic properties in a rabbit seizure model. Following intranasal infection, 40% of the rabbits infected with the gI-deleted virus showed severe neurological signs. gI-deleted BHV-5 invaded all the central nervous system (CNS) structures invaded by the gI-revertant BHV-5; however, the number of neurons infected by the gI-deleted virus was similar or slightly reduced (two to four fold). Thus, the gI-deleted virus retained significant neurovirulence and/or neuroinvasive properties when compared with the gE-deleted BHV-5. Pulse-chase analysis revealed that the gE of gI-deleted virus was processed to a larger and a diffused 94- to 100-kDa protein (instead of 94 kDa). The 94- to 100-kDa protein was processed in the Golgi with delayed kinetics but it was endoglycosidase H (EndoH) resistant. In cells infected with gI-deleted virus, there was a reduction in cell-surface gE expression compared to wild-type, which correlated to reduced amount of gE processed in the Golgi. The authors believe that in the absence of gI, BHV-5 gE is sufficient for BHV-5 neurovirulence.
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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/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Envelope Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/glycoprotein E, bovine herpesvirus...,
http://linkedlifedata.com/resource/pubmed/chemical/glycoprotein gp1, varicella-zoster...
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1355-0284
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
233-43
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15371153-Animals,
pubmed-meshheading:15371153-Cattle,
pubmed-meshheading:15371153-Cattle Diseases,
pubmed-meshheading:15371153-DNA Primers,
pubmed-meshheading:15371153-Gene Deletion,
pubmed-meshheading:15371153-Herpesviridae Infections,
pubmed-meshheading:15371153-Herpesvirus 5, Bovine,
pubmed-meshheading:15371153-Meningoencephalitis,
pubmed-meshheading:15371153-Molecular Sequence Data,
pubmed-meshheading:15371153-Polymerase Chain Reaction,
pubmed-meshheading:15371153-Recombination, Genetic,
pubmed-meshheading:15371153-Viral Envelope Proteins,
pubmed-meshheading:15371153-Virulence
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pubmed:year |
2004
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pubmed:articleTitle |
In the absence of glycoprotein I (gI), gE determines bovine herpesvirus type 5 neuroinvasiveness and neurovirulence.
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pubmed:affiliation |
Department of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan 66506, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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