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Porcine Circovirus Type 2 ORF5 Protein Induces Autophagy to Promote Viral Replication via the PERK-eIF2α-ATF4 and mTOR-ERK1/2-AMPK Signaling Pathways in PK-15 Cells

Porcine circovirus type 2 (PCV2) is the primary causative agent that causing porcine circovirus-associated disease (PCVAD). The open reading frame 5 (ORF5) protein is a newly discovered non-structural protein in PCV2, which the function in viral pathogenesis remains unknown. The aim of this study wa...

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Autores principales: Lv, Jiangman, Jiang, Yanfen, Feng, Quanwen, Fan, Zhixin, Sun, Ying, Xu, Panpan, Hou, Yufeng, Zhang, Xiuping, Fan, Yuxin, Xu, Xingang, Zhang, Yanming, Guo, Kangkang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058596/
https://www.ncbi.nlm.nih.gov/pubmed/32184774
http://dx.doi.org/10.3389/fmicb.2020.00320
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author Lv, Jiangman
Jiang, Yanfen
Feng, Quanwen
Fan, Zhixin
Sun, Ying
Xu, Panpan
Hou, Yufeng
Zhang, Xiuping
Fan, Yuxin
Xu, Xingang
Zhang, Yanming
Guo, Kangkang
author_facet Lv, Jiangman
Jiang, Yanfen
Feng, Quanwen
Fan, Zhixin
Sun, Ying
Xu, Panpan
Hou, Yufeng
Zhang, Xiuping
Fan, Yuxin
Xu, Xingang
Zhang, Yanming
Guo, Kangkang
author_sort Lv, Jiangman
collection PubMed
description Porcine circovirus type 2 (PCV2) is the primary causative agent that causing porcine circovirus-associated disease (PCVAD). The open reading frame 5 (ORF5) protein is a newly discovered non-structural protein in PCV2, which the function in viral pathogenesis remains unknown. The aim of this study was to investigate the mechanism of PCV2 ORF5 protein on autophagy and viral replication. The pEGFP-tagged ORF5 gene was ectopic expressed in PK-15 cells and an ORF5-deficient PCV2 mutant strain (PCV2(ΔORF5)) were used to infected PK-15 cells. This study demonstrated that the ORF5 is essential for the of PCV2-induced autophagy. The ORF5 protein triggers the phosphorylation of PERK, eIF2α and the expression of downstream transcription factor ATF4. In addition, ORF5 protein activated the AMPK-ERK1/2-mTOR signaling pathways. These findings suggest that ORF5 play essential roles in the induction of autophagy by PCV2. We further revealed that PCV2 ORF5 promotes viral replication through PERK-eIF2α-ATF4 and AMPK-ERK1/2-mTOR pathways. In conclusion, we showed that PCV2 ORF5 induces autophagy to promote virus replication in PK-15 cells.
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spelling pubmed-70585962020-03-17 Porcine Circovirus Type 2 ORF5 Protein Induces Autophagy to Promote Viral Replication via the PERK-eIF2α-ATF4 and mTOR-ERK1/2-AMPK Signaling Pathways in PK-15 Cells Lv, Jiangman Jiang, Yanfen Feng, Quanwen Fan, Zhixin Sun, Ying Xu, Panpan Hou, Yufeng Zhang, Xiuping Fan, Yuxin Xu, Xingang Zhang, Yanming Guo, Kangkang Front Microbiol Microbiology Porcine circovirus type 2 (PCV2) is the primary causative agent that causing porcine circovirus-associated disease (PCVAD). The open reading frame 5 (ORF5) protein is a newly discovered non-structural protein in PCV2, which the function in viral pathogenesis remains unknown. The aim of this study was to investigate the mechanism of PCV2 ORF5 protein on autophagy and viral replication. The pEGFP-tagged ORF5 gene was ectopic expressed in PK-15 cells and an ORF5-deficient PCV2 mutant strain (PCV2(ΔORF5)) were used to infected PK-15 cells. This study demonstrated that the ORF5 is essential for the of PCV2-induced autophagy. The ORF5 protein triggers the phosphorylation of PERK, eIF2α and the expression of downstream transcription factor ATF4. In addition, ORF5 protein activated the AMPK-ERK1/2-mTOR signaling pathways. These findings suggest that ORF5 play essential roles in the induction of autophagy by PCV2. We further revealed that PCV2 ORF5 promotes viral replication through PERK-eIF2α-ATF4 and AMPK-ERK1/2-mTOR pathways. In conclusion, we showed that PCV2 ORF5 induces autophagy to promote virus replication in PK-15 cells. Frontiers Media S.A. 2020-02-28 /pmc/articles/PMC7058596/ /pubmed/32184774 http://dx.doi.org/10.3389/fmicb.2020.00320 Text en Copyright © 2020 Lv, Jiang, Feng, Fan, Sun, Xu, Hou, Zhang, Fan, Xu, Zhang and Guo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Lv, Jiangman
Jiang, Yanfen
Feng, Quanwen
Fan, Zhixin
Sun, Ying
Xu, Panpan
Hou, Yufeng
Zhang, Xiuping
Fan, Yuxin
Xu, Xingang
Zhang, Yanming
Guo, Kangkang
Porcine Circovirus Type 2 ORF5 Protein Induces Autophagy to Promote Viral Replication via the PERK-eIF2α-ATF4 and mTOR-ERK1/2-AMPK Signaling Pathways in PK-15 Cells
title Porcine Circovirus Type 2 ORF5 Protein Induces Autophagy to Promote Viral Replication via the PERK-eIF2α-ATF4 and mTOR-ERK1/2-AMPK Signaling Pathways in PK-15 Cells
title_full Porcine Circovirus Type 2 ORF5 Protein Induces Autophagy to Promote Viral Replication via the PERK-eIF2α-ATF4 and mTOR-ERK1/2-AMPK Signaling Pathways in PK-15 Cells
title_fullStr Porcine Circovirus Type 2 ORF5 Protein Induces Autophagy to Promote Viral Replication via the PERK-eIF2α-ATF4 and mTOR-ERK1/2-AMPK Signaling Pathways in PK-15 Cells
title_full_unstemmed Porcine Circovirus Type 2 ORF5 Protein Induces Autophagy to Promote Viral Replication via the PERK-eIF2α-ATF4 and mTOR-ERK1/2-AMPK Signaling Pathways in PK-15 Cells
title_short Porcine Circovirus Type 2 ORF5 Protein Induces Autophagy to Promote Viral Replication via the PERK-eIF2α-ATF4 and mTOR-ERK1/2-AMPK Signaling Pathways in PK-15 Cells
title_sort porcine circovirus type 2 orf5 protein induces autophagy to promote viral replication via the perk-eif2α-atf4 and mtor-erk1/2-ampk signaling pathways in pk-15 cells
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058596/
https://www.ncbi.nlm.nih.gov/pubmed/32184774
http://dx.doi.org/10.3389/fmicb.2020.00320
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