AcMNPV core gene ac109 is required for budded virion transport to the nucleus and for occlusion of viral progeny.

The Autographa californica multiple nucleopolyhedrovirus (AcMNPV) ac109 core gene has been previously characterized as an essential late gene. Our results showed that budded virions could be detected in supernatants of infected Sf-9 cells, even when ac109 knockout viruses displayed a single-cell inf...

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Main Authors: Victoria Alfonso, Guillermo A Maroniche, Sol R Reca, María Gabriela López, Mariana del Vas, Oscar Taboga
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3458853?pdf=render
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spelling doaj-b7fde1a2b7694966bc9092bd9643eaaf2020-11-25T01:25:06ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4614610.1371/journal.pone.0046146AcMNPV core gene ac109 is required for budded virion transport to the nucleus and for occlusion of viral progeny.Victoria AlfonsoGuillermo A MaronicheSol R RecaMaría Gabriela LópezMariana del VasOscar TabogaThe Autographa californica multiple nucleopolyhedrovirus (AcMNPV) ac109 core gene has been previously characterized as an essential late gene. Our results showed that budded virions could be detected in supernatants of infected Sf-9 cells, even when ac109 knockout viruses displayed a single-cell infection phenotype. Moreover, confocal microscopy analysis revealed that budded virions can enter the cytoplasm but are unable to enter the cell nucleus. This defect could be repaired by complementing ac109 in trans. In addition, polyhedra of normal size could be detected in Sf-9 nuclei infected with ac109 knockout viruses. However, electron microscopy demonstrated that these occlusion bodies were empty. Altogether, these results indicate that ac109 is required for infectivity of both phenotypes of virus.http://europepmc.org/articles/PMC3458853?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Victoria Alfonso
Guillermo A Maroniche
Sol R Reca
María Gabriela López
Mariana del Vas
Oscar Taboga
spellingShingle Victoria Alfonso
Guillermo A Maroniche
Sol R Reca
María Gabriela López
Mariana del Vas
Oscar Taboga
AcMNPV core gene ac109 is required for budded virion transport to the nucleus and for occlusion of viral progeny.
PLoS ONE
author_facet Victoria Alfonso
Guillermo A Maroniche
Sol R Reca
María Gabriela López
Mariana del Vas
Oscar Taboga
author_sort Victoria Alfonso
title AcMNPV core gene ac109 is required for budded virion transport to the nucleus and for occlusion of viral progeny.
title_short AcMNPV core gene ac109 is required for budded virion transport to the nucleus and for occlusion of viral progeny.
title_full AcMNPV core gene ac109 is required for budded virion transport to the nucleus and for occlusion of viral progeny.
title_fullStr AcMNPV core gene ac109 is required for budded virion transport to the nucleus and for occlusion of viral progeny.
title_full_unstemmed AcMNPV core gene ac109 is required for budded virion transport to the nucleus and for occlusion of viral progeny.
title_sort acmnpv core gene ac109 is required for budded virion transport to the nucleus and for occlusion of viral progeny.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The Autographa californica multiple nucleopolyhedrovirus (AcMNPV) ac109 core gene has been previously characterized as an essential late gene. Our results showed that budded virions could be detected in supernatants of infected Sf-9 cells, even when ac109 knockout viruses displayed a single-cell infection phenotype. Moreover, confocal microscopy analysis revealed that budded virions can enter the cytoplasm but are unable to enter the cell nucleus. This defect could be repaired by complementing ac109 in trans. In addition, polyhedra of normal size could be detected in Sf-9 nuclei infected with ac109 knockout viruses. However, electron microscopy demonstrated that these occlusion bodies were empty. Altogether, these results indicate that ac109 is required for infectivity of both phenotypes of virus.
url http://europepmc.org/articles/PMC3458853?pdf=render
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