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A conditional-lethal vaccinia virus mutant demonstrates that the I7L gene product is required for virion morphogenesis

A conditional-lethal recombinant virus was constructed in which the expression of the vaccinia virus I7L gene is under the control of the tetracycline operator/repressor system. In the absence of I7L expression, processing of the major VV core proteins is inhibited and electron microscopy reveals de...

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Detalles Bibliográficos
Autores principales: Byrd, Chelsea M, Hruby, Dennis E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548685/
https://www.ncbi.nlm.nih.gov/pubmed/15701171
http://dx.doi.org/10.1186/1743-422X-2-4
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author Byrd, Chelsea M
Hruby, Dennis E
author_facet Byrd, Chelsea M
Hruby, Dennis E
author_sort Byrd, Chelsea M
collection PubMed
description A conditional-lethal recombinant virus was constructed in which the expression of the vaccinia virus I7L gene is under the control of the tetracycline operator/repressor system. In the absence of I7L expression, processing of the major VV core proteins is inhibited and electron microscopy reveals defects in virion morphogenesis subsequent to the formation of immature virion particles but prior to core condensation. Plasmid-borne I7L is capable of rescuing the growth of this virus and rescue is optimal when the I7L gene is expressed using the authentic I7L promoter. Taken together, these data suggest that correct temporal expression of the VV I7L cysteine proteinase is required for core protein maturation, virion assembly and production of infectious progeny.
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spelling pubmed-5486852005-02-13 A conditional-lethal vaccinia virus mutant demonstrates that the I7L gene product is required for virion morphogenesis Byrd, Chelsea M Hruby, Dennis E Virol J Short Report A conditional-lethal recombinant virus was constructed in which the expression of the vaccinia virus I7L gene is under the control of the tetracycline operator/repressor system. In the absence of I7L expression, processing of the major VV core proteins is inhibited and electron microscopy reveals defects in virion morphogenesis subsequent to the formation of immature virion particles but prior to core condensation. Plasmid-borne I7L is capable of rescuing the growth of this virus and rescue is optimal when the I7L gene is expressed using the authentic I7L promoter. Taken together, these data suggest that correct temporal expression of the VV I7L cysteine proteinase is required for core protein maturation, virion assembly and production of infectious progeny. BioMed Central 2005-02-08 /pmc/articles/PMC548685/ /pubmed/15701171 http://dx.doi.org/10.1186/1743-422X-2-4 Text en Copyright © 2005 Byrd and Hruby; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Byrd, Chelsea M
Hruby, Dennis E
A conditional-lethal vaccinia virus mutant demonstrates that the I7L gene product is required for virion morphogenesis
title A conditional-lethal vaccinia virus mutant demonstrates that the I7L gene product is required for virion morphogenesis
title_full A conditional-lethal vaccinia virus mutant demonstrates that the I7L gene product is required for virion morphogenesis
title_fullStr A conditional-lethal vaccinia virus mutant demonstrates that the I7L gene product is required for virion morphogenesis
title_full_unstemmed A conditional-lethal vaccinia virus mutant demonstrates that the I7L gene product is required for virion morphogenesis
title_short A conditional-lethal vaccinia virus mutant demonstrates that the I7L gene product is required for virion morphogenesis
title_sort conditional-lethal vaccinia virus mutant demonstrates that the i7l gene product is required for virion morphogenesis
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548685/
https://www.ncbi.nlm.nih.gov/pubmed/15701171
http://dx.doi.org/10.1186/1743-422X-2-4
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