Source:http://linkedlifedata.com/resource/pubmed/id/21697348
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
Pt 10
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pubmed:dateCreated |
2011-9-20
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pubmed:abstractText |
Elucidating the cellular and molecular factors governing herpes simplex virus type 1 (HSV-1) neurotropism is a prerequisite for understanding HSV-1 encephalitis and for targeting HSV-1-derived vectors for gene transfer to the brain. Earlier we had described an ex vivo system of mouse brain slices and demonstrated a selective and unique infection pattern, mostly around the ventricles. Here, we examined tissue factors controlling HSV-1 infection of brain slices. We demonstrated that heparan sulphate, while an important factor, does not determine the infection pattern. Hyaluronic acid, but not collagen, appears to enhance HSV-1 brain infection. To investigate whether tissue distribution of viral receptors determines the infection pattern, we examined transcription of herpes virus entry mediator and nectin-1 receptor genes in infected and uninfected brain regions. Both the infected and the uninfected regions express the receptors. We also explored the influence of intra-cellular factors. HSV-1 does not preferentially infect proliferating cells in the brain slices, despite its predilection to the ventricular zones. To delineate the step at which the HSV-1 infection cascade is restricted, mRNA was isolated following tissue infection, and transcription of the immediate-early and late viral genes was evaluated. The results indicated that HSV-1 genes are not expressed in regions that do not express a viral reporter gene. Therefore, we conclude that tissue resistance to infection is associated with a block at or prior to the immediate-early mRNA synthesis. Taken together, using the ex vivo system of organotypic culture we describe here extra-cellular and intra-cellular restriction levels of HSV-1 brain infection.
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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 |
Oct
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pubmed:issn |
1465-2099
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
92
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2383-93
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pubmed:meshHeading |
pubmed-meshheading:21697348-Animals,
pubmed-meshheading:21697348-Brain,
pubmed-meshheading:21697348-Disease Models, Animal,
pubmed-meshheading:21697348-Encephalitis, Herpes Simplex,
pubmed-meshheading:21697348-Gene Expression Profiling,
pubmed-meshheading:21697348-Herpesvirus 1, Human,
pubmed-meshheading:21697348-Mice,
pubmed-meshheading:21697348-Mice, Inbred BALB C,
pubmed-meshheading:21697348-RNA, Viral,
pubmed-meshheading:21697348-Receptors, Virus,
pubmed-meshheading:21697348-Viral Tropism,
pubmed-meshheading:21697348-Virus Replication
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pubmed:year |
2011
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pubmed:articleTitle |
Restrictions that control herpes simplex virus type 1 infection in mouse brain ex vivo.
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pubmed:affiliation |
Laboratory of Neurovirology, IMRIC, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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