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Clathrin-mediated endocytosis is a candidate entry sorting mechanism for Bombyx mori cypovirus

Bombyx mori cypovirus (BmCPV), a member of the Reoviridae, specifically infects silkworms and causes extensive economic losses to the sericulture industry. To date, the entry mechanism of BmCPV into cells is unclear. Here we used electron microscopy to study the route of entry of BmCPV into cells, a...

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Autores principales: Chen, Fei, Zhu, Liyuan, Zhang, Yiling, Kumar, Dhiraj, Cao, Guangli, Hu, Xiaolong, Liang, Zi, Kuang, Sulan, Xue, Renyu, Gong, Chengliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940776/
https://www.ncbi.nlm.nih.gov/pubmed/29740149
http://dx.doi.org/10.1038/s41598-018-25677-1
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author Chen, Fei
Zhu, Liyuan
Zhang, Yiling
Kumar, Dhiraj
Cao, Guangli
Hu, Xiaolong
Liang, Zi
Kuang, Sulan
Xue, Renyu
Gong, Chengliang
author_facet Chen, Fei
Zhu, Liyuan
Zhang, Yiling
Kumar, Dhiraj
Cao, Guangli
Hu, Xiaolong
Liang, Zi
Kuang, Sulan
Xue, Renyu
Gong, Chengliang
author_sort Chen, Fei
collection PubMed
description Bombyx mori cypovirus (BmCPV), a member of the Reoviridae, specifically infects silkworms and causes extensive economic losses to the sericulture industry. To date, the entry mechanism of BmCPV into cells is unclear. Here we used electron microscopy to study the route of entry of BmCPV into cells, and the results demonstrated that the entry of BmCPV into BmN cells was mediated by endocytosis. Blocking the entry pathway with four endocytosis inhibitors, including dansylcadaverine, chlorpromazine, genistein, and PP2, significantly decreased the infectivity of BmCPV. This indicates that BmCPV enters BmN cells via endocytosis, and that clathrin-mediated sorting is the predominant entry method. After the relative expression levels of clathrin heavy chain (clathrin, GenBank accession No. NM_001142971.1) and the adaptor protein complex-1 gamma subunit AP-1 (AP-1, GenBank accession No. JQ824201.1), which are involved in clathrin-mediated endocytosis, were inhibited by RNA interference or abolishing the functions of clathrin and AP-1 with their corresponding antibodies, the infectivity of BmCPV was reduced significantly, which suggests that clathrin-mediated endocytosis contributed to the entry of BmCPV into cells. Our findings suggest that the clathrin-mediated endocytosis pathway is a candidate for the development of therapeutics for silkworm cytoplasmic polyhedrosis.
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spelling pubmed-59407762018-05-11 Clathrin-mediated endocytosis is a candidate entry sorting mechanism for Bombyx mori cypovirus Chen, Fei Zhu, Liyuan Zhang, Yiling Kumar, Dhiraj Cao, Guangli Hu, Xiaolong Liang, Zi Kuang, Sulan Xue, Renyu Gong, Chengliang Sci Rep Article Bombyx mori cypovirus (BmCPV), a member of the Reoviridae, specifically infects silkworms and causes extensive economic losses to the sericulture industry. To date, the entry mechanism of BmCPV into cells is unclear. Here we used electron microscopy to study the route of entry of BmCPV into cells, and the results demonstrated that the entry of BmCPV into BmN cells was mediated by endocytosis. Blocking the entry pathway with four endocytosis inhibitors, including dansylcadaverine, chlorpromazine, genistein, and PP2, significantly decreased the infectivity of BmCPV. This indicates that BmCPV enters BmN cells via endocytosis, and that clathrin-mediated sorting is the predominant entry method. After the relative expression levels of clathrin heavy chain (clathrin, GenBank accession No. NM_001142971.1) and the adaptor protein complex-1 gamma subunit AP-1 (AP-1, GenBank accession No. JQ824201.1), which are involved in clathrin-mediated endocytosis, were inhibited by RNA interference or abolishing the functions of clathrin and AP-1 with their corresponding antibodies, the infectivity of BmCPV was reduced significantly, which suggests that clathrin-mediated endocytosis contributed to the entry of BmCPV into cells. Our findings suggest that the clathrin-mediated endocytosis pathway is a candidate for the development of therapeutics for silkworm cytoplasmic polyhedrosis. Nature Publishing Group UK 2018-05-08 /pmc/articles/PMC5940776/ /pubmed/29740149 http://dx.doi.org/10.1038/s41598-018-25677-1 Text en © The Author(s) 2018 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
Chen, Fei
Zhu, Liyuan
Zhang, Yiling
Kumar, Dhiraj
Cao, Guangli
Hu, Xiaolong
Liang, Zi
Kuang, Sulan
Xue, Renyu
Gong, Chengliang
Clathrin-mediated endocytosis is a candidate entry sorting mechanism for Bombyx mori cypovirus
title Clathrin-mediated endocytosis is a candidate entry sorting mechanism for Bombyx mori cypovirus
title_full Clathrin-mediated endocytosis is a candidate entry sorting mechanism for Bombyx mori cypovirus
title_fullStr Clathrin-mediated endocytosis is a candidate entry sorting mechanism for Bombyx mori cypovirus
title_full_unstemmed Clathrin-mediated endocytosis is a candidate entry sorting mechanism for Bombyx mori cypovirus
title_short Clathrin-mediated endocytosis is a candidate entry sorting mechanism for Bombyx mori cypovirus
title_sort clathrin-mediated endocytosis is a candidate entry sorting mechanism for bombyx mori cypovirus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940776/
https://www.ncbi.nlm.nih.gov/pubmed/29740149
http://dx.doi.org/10.1038/s41598-018-25677-1
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