Fowl plague virus replication in mammalian cell-avian erythrocyte heterokaryons: Studies concerning the actinomycin D and ultra-violet light sensitive phase in influenza virus replication
Identifieur interne : 002C14 ( Main/Exploration ); précédent : 002C13; suivant : 002C15Fowl plague virus replication in mammalian cell-avian erythrocyte heterokaryons: Studies concerning the actinomycin D and ultra-violet light sensitive phase in influenza virus replication
Auteurs : D. C. Kelly [Royaume-Uni] ; N. J. Dimmock [Royaume-Uni]Source :
- Virology [ 0042-6822 ] ; 1974.
English descriptors
- Teeft :
- Actinomycin, Avian, Avian erythrocyte nuclei, Avian erythrocyte nucleus, Avian erythrocytes, Cell nucleus, Cytoplasmic fluorescence, Dimmock, Erythrocyte, Erythrocyte heterokaryon, Erythrocyte nuclei, Erythrocyte nucleus, Fowl, Fowl plague, Fowl plague virus, Functional nucleolus, Haemagglutinin, Heterokaryon, Heterokaryons, Infectious virus, Influenza, Influenza virus, Influenza virus infection, Influenza virus replication, Influenza viruses, Kelly, Mammalian cells, Monochromatic light, Nucleolus, Nucleus, Polymerase, Polymerase activity, Postfusion, Replication, Room temperature, Sendai, Sendai virus, Ultraviolet irradiation, Ultraviolet light, Unpublished results, Various wavelengths, Virology, Virus, Virus suspension.
Abstract
Abstract: The replication of fowl plague virus in BHK and L cells specifically blocked prior to infection with inhibitors of influenza virus replication (actinomycin D and ultraviolet light irradiation) has been studied by the introduction of a metabolically dormant avian erythrocyte nucleus. This permits the synthesis of just the influenza virus nucleoprotein in actinomycin D (but not ultraviolet light) blocked cells. The NP antigen is first detected in the avian erythrocyte nucleus and subsequently in the heterokaryon cytoplasm.
Url:
DOI: 10.1016/0042-6822(74)90255-4
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream Istex, to step Curation: 001322
- to stream Istex, to step Checkpoint: 001769
- to stream Main, to step Merge: 002D88
- to stream Main, to step Curation: 002C14
Le document en format XML
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<term>Avian erythrocyte nuclei</term>
<term>Avian erythrocyte nucleus</term>
<term>Avian erythrocytes</term>
<term>Cell nucleus</term>
<term>Cytoplasmic fluorescence</term>
<term>Dimmock</term>
<term>Erythrocyte</term>
<term>Erythrocyte heterokaryon</term>
<term>Erythrocyte nuclei</term>
<term>Erythrocyte nucleus</term>
<term>Fowl</term>
<term>Fowl plague</term>
<term>Fowl plague virus</term>
<term>Functional nucleolus</term>
<term>Haemagglutinin</term>
<term>Heterokaryon</term>
<term>Heterokaryons</term>
<term>Infectious virus</term>
<term>Influenza</term>
<term>Influenza virus</term>
<term>Influenza virus infection</term>
<term>Influenza virus replication</term>
<term>Influenza viruses</term>
<term>Kelly</term>
<term>Mammalian cells</term>
<term>Monochromatic light</term>
<term>Nucleolus</term>
<term>Nucleus</term>
<term>Polymerase</term>
<term>Polymerase activity</term>
<term>Postfusion</term>
<term>Replication</term>
<term>Room temperature</term>
<term>Sendai</term>
<term>Sendai virus</term>
<term>Ultraviolet irradiation</term>
<term>Ultraviolet light</term>
<term>Unpublished results</term>
<term>Various wavelengths</term>
<term>Virology</term>
<term>Virus</term>
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<front><div type="abstract" xml:lang="en">Abstract: The replication of fowl plague virus in BHK and L cells specifically blocked prior to infection with inhibitors of influenza virus replication (actinomycin D and ultraviolet light irradiation) has been studied by the introduction of a metabolically dormant avian erythrocyte nucleus. This permits the synthesis of just the influenza virus nucleoprotein in actinomycin D (but not ultraviolet light) blocked cells. The NP antigen is first detected in the avian erythrocyte nucleus and subsequently in the heterokaryon cytoplasm.</div>
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