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Nonstructural proteins 2C and 3D are involved in autophagy as induced by the encephalomyocarditis virus

BACKGROUND: Encephalomyocarditis virus (EMCV) can infect a variety of animal species and humans. Although the EMCV infection is known to induce autophagy to promote its replication in host cells, the viral proteins that are responsible for inducing autophagy are unknown. METHODS: The recombinant pla...

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Autores principales: Hou, Lei, Ge, Xinna, Xin, Lingxiang, Zhou, Lei, Guo, Xin, Yang, Hanchun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161894/
https://www.ncbi.nlm.nih.gov/pubmed/25178311
http://dx.doi.org/10.1186/1743-422X-11-156
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author Hou, Lei
Ge, Xinna
Xin, Lingxiang
Zhou, Lei
Guo, Xin
Yang, Hanchun
author_facet Hou, Lei
Ge, Xinna
Xin, Lingxiang
Zhou, Lei
Guo, Xin
Yang, Hanchun
author_sort Hou, Lei
collection PubMed
description BACKGROUND: Encephalomyocarditis virus (EMCV) can infect a variety of animal species and humans. Although the EMCV infection is known to induce autophagy to promote its replication in host cells, the viral proteins that are responsible for inducing autophagy are unknown. METHODS: The recombinant plasmids that were expressing the EMCV proteins were constructed to analyze the role of each protein in the induction of autophagy. Autophagy inductions by the EMCV proteins in BHK-21 cells were investigated by confocal microscopy, Western blotting and transmission electron microscopy. ER stress in BHK-21 cells was examined by detecting the marker molecules using western blotting and luciferase assays. RESULTS: This study presents the first demonstration that the nonstructural proteins 2C or 3D of EMCV were involved in inducing autophagy in BHK-21 cells that were expressing 2C or 3D, and we found that inhibiting Beclin1 expression influenced this autophagy induction process. Next, 2C and 3D were shown to be involved in inducing autophagy by activating the ER stress pathway. Finally, EMCV 2C or 3D were demonstrated to regulate the proteins associated with PERK and ATF6alpha pathway. CONCLUSIONS: Our findings indicate that 2C and 3D are involved in EMCV-induced autophagy by activating ER stress molecules and regulating the proteins expression associated with UPR pathway, helping to better understand the EMCV-induced autophagy process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1743-422X-11-156) contains supplementary material, which is available to authorized users.
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spelling pubmed-41618942014-09-13 Nonstructural proteins 2C and 3D are involved in autophagy as induced by the encephalomyocarditis virus Hou, Lei Ge, Xinna Xin, Lingxiang Zhou, Lei Guo, Xin Yang, Hanchun Virol J Research BACKGROUND: Encephalomyocarditis virus (EMCV) can infect a variety of animal species and humans. Although the EMCV infection is known to induce autophagy to promote its replication in host cells, the viral proteins that are responsible for inducing autophagy are unknown. METHODS: The recombinant plasmids that were expressing the EMCV proteins were constructed to analyze the role of each protein in the induction of autophagy. Autophagy inductions by the EMCV proteins in BHK-21 cells were investigated by confocal microscopy, Western blotting and transmission electron microscopy. ER stress in BHK-21 cells was examined by detecting the marker molecules using western blotting and luciferase assays. RESULTS: This study presents the first demonstration that the nonstructural proteins 2C or 3D of EMCV were involved in inducing autophagy in BHK-21 cells that were expressing 2C or 3D, and we found that inhibiting Beclin1 expression influenced this autophagy induction process. Next, 2C and 3D were shown to be involved in inducing autophagy by activating the ER stress pathway. Finally, EMCV 2C or 3D were demonstrated to regulate the proteins associated with PERK and ATF6alpha pathway. CONCLUSIONS: Our findings indicate that 2C and 3D are involved in EMCV-induced autophagy by activating ER stress molecules and regulating the proteins expression associated with UPR pathway, helping to better understand the EMCV-induced autophagy process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1743-422X-11-156) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-01 /pmc/articles/PMC4161894/ /pubmed/25178311 http://dx.doi.org/10.1186/1743-422X-11-156 Text en © Hou et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Hou, Lei
Ge, Xinna
Xin, Lingxiang
Zhou, Lei
Guo, Xin
Yang, Hanchun
Nonstructural proteins 2C and 3D are involved in autophagy as induced by the encephalomyocarditis virus
title Nonstructural proteins 2C and 3D are involved in autophagy as induced by the encephalomyocarditis virus
title_full Nonstructural proteins 2C and 3D are involved in autophagy as induced by the encephalomyocarditis virus
title_fullStr Nonstructural proteins 2C and 3D are involved in autophagy as induced by the encephalomyocarditis virus
title_full_unstemmed Nonstructural proteins 2C and 3D are involved in autophagy as induced by the encephalomyocarditis virus
title_short Nonstructural proteins 2C and 3D are involved in autophagy as induced by the encephalomyocarditis virus
title_sort nonstructural proteins 2c and 3d are involved in autophagy as induced by the encephalomyocarditis virus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161894/
https://www.ncbi.nlm.nih.gov/pubmed/25178311
http://dx.doi.org/10.1186/1743-422X-11-156
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