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Baculovirus infection induces disruption of the nuclear lamina

Baculovirus nucleocapsids egress from the nucleus primarily via budding at the nuclear membrane. The nuclear lamina underlying the nuclear membrane represents a substantial barrier to nuclear egress. Whether the nuclear lamina undergoes disruption during baculovirus infection remains unknown. In thi...

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Autores principales: Zhang, Xiaomei, Xu, Kaiyan, Wei, Denghui, Wu, Wenbi, Yang, Kai, Yuan, Meijin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552856/
https://www.ncbi.nlm.nih.gov/pubmed/28798307
http://dx.doi.org/10.1038/s41598-017-08437-5
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author Zhang, Xiaomei
Xu, Kaiyan
Wei, Denghui
Wu, Wenbi
Yang, Kai
Yuan, Meijin
author_facet Zhang, Xiaomei
Xu, Kaiyan
Wei, Denghui
Wu, Wenbi
Yang, Kai
Yuan, Meijin
author_sort Zhang, Xiaomei
collection PubMed
description Baculovirus nucleocapsids egress from the nucleus primarily via budding at the nuclear membrane. The nuclear lamina underlying the nuclear membrane represents a substantial barrier to nuclear egress. Whether the nuclear lamina undergoes disruption during baculovirus infection remains unknown. In this report, we generated a clonal cell line, Sf9-L, that stably expresses GFP-tagged Drosophila lamin B. GFP autofluorescence colocalized with immunofluorescent anti-lamin B at the nuclear rim of Sf9-L cells, indicating GFP-lamin B was incorporated into the nuclear lamina. Meanwhile, virus was able to replicate normally in Sf9-L cells. Next, we investigated alterations to the nuclear lamina during baculovirus infection in Sf9-L cells. A portion of GFP-lamin B localized diffusely at the nuclear rim, and some GFP-lamin B was redistributed within the nucleus during the late phase of infection, suggesting the nuclear lamina was partially disrupted. Immunoelectron microscopy revealed associations between GFP-lamin B and the edges of the electron-dense stromal mattes of the virogenic stroma, intranuclear microvesicles, and ODV envelopes and nucleocapsids within the nucleus, indicating the release of some GFP-lamin B from the nuclear lamina. Additionally, GFP-lamin B phosphorylation increased upon infection. Based on these data, baculovirus infection induced lamin B phosphorylation and disruption of the nuclear lamina.
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spelling pubmed-55528562017-08-14 Baculovirus infection induces disruption of the nuclear lamina Zhang, Xiaomei Xu, Kaiyan Wei, Denghui Wu, Wenbi Yang, Kai Yuan, Meijin Sci Rep Article Baculovirus nucleocapsids egress from the nucleus primarily via budding at the nuclear membrane. The nuclear lamina underlying the nuclear membrane represents a substantial barrier to nuclear egress. Whether the nuclear lamina undergoes disruption during baculovirus infection remains unknown. In this report, we generated a clonal cell line, Sf9-L, that stably expresses GFP-tagged Drosophila lamin B. GFP autofluorescence colocalized with immunofluorescent anti-lamin B at the nuclear rim of Sf9-L cells, indicating GFP-lamin B was incorporated into the nuclear lamina. Meanwhile, virus was able to replicate normally in Sf9-L cells. Next, we investigated alterations to the nuclear lamina during baculovirus infection in Sf9-L cells. A portion of GFP-lamin B localized diffusely at the nuclear rim, and some GFP-lamin B was redistributed within the nucleus during the late phase of infection, suggesting the nuclear lamina was partially disrupted. Immunoelectron microscopy revealed associations between GFP-lamin B and the edges of the electron-dense stromal mattes of the virogenic stroma, intranuclear microvesicles, and ODV envelopes and nucleocapsids within the nucleus, indicating the release of some GFP-lamin B from the nuclear lamina. Additionally, GFP-lamin B phosphorylation increased upon infection. Based on these data, baculovirus infection induced lamin B phosphorylation and disruption of the nuclear lamina. Nature Publishing Group UK 2017-08-10 /pmc/articles/PMC5552856/ /pubmed/28798307 http://dx.doi.org/10.1038/s41598-017-08437-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhang, Xiaomei
Xu, Kaiyan
Wei, Denghui
Wu, Wenbi
Yang, Kai
Yuan, Meijin
Baculovirus infection induces disruption of the nuclear lamina
title Baculovirus infection induces disruption of the nuclear lamina
title_full Baculovirus infection induces disruption of the nuclear lamina
title_fullStr Baculovirus infection induces disruption of the nuclear lamina
title_full_unstemmed Baculovirus infection induces disruption of the nuclear lamina
title_short Baculovirus infection induces disruption of the nuclear lamina
title_sort baculovirus infection induces disruption of the nuclear lamina
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552856/
https://www.ncbi.nlm.nih.gov/pubmed/28798307
http://dx.doi.org/10.1038/s41598-017-08437-5
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