Cargando…
miR-214–5p/C1QTNF1 axis enhances PCV2 replication through promoting autophagy by targeting AKT/mTOR signaling pathway
Porcine circovirus type 2 (PCV2) is the causative agent of PCV2-associated disease, which causes a relevant economic impact on the global swine industry. Accumulating data have indicated host microRNAs play essential roles in numerous virus replication of pigs, while their roles in PCV2 replication...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194317/ https://www.ncbi.nlm.nih.gov/pubmed/36302471 http://dx.doi.org/10.1016/j.virusres.2022.198990 |
_version_ | 1785043991909105664 |
---|---|
author | Cao, Yue Jing, Pengfei Yu, Luchen Wu, Zhengchang Gao, Song Bao, Wenbin |
author_facet | Cao, Yue Jing, Pengfei Yu, Luchen Wu, Zhengchang Gao, Song Bao, Wenbin |
author_sort | Cao, Yue |
collection | PubMed |
description | Porcine circovirus type 2 (PCV2) is the causative agent of PCV2-associated disease, which causes a relevant economic impact on the global swine industry. Accumulating data have indicated host microRNAs play essential roles in numerous virus replication of pigs, while their roles in PCV2 replication remain unclear. Herein, we demonstrated that PCV2 infection downregulated the expression of miR-214–5p in PK15 cells, and miR-214–5p promoted PCV2 replication. C1q/tumor necrosis factor-related protein 1 (C1QTNF1) was then identified as a target gene of miR-214–5p, and C1QTNF1 suppressed PCV2 replication. Interestingly, miR-214–5p/C1QTNF1 axis negatively regulated AKT/mTOR signaling, and then enhanced PCV2 replication through promoting autophagy in PK15 cells. Collectively, our findings provide insight into the mechanism of PCV2 replication and highlight miR-214–5p and C1QTNF1 as potential novel targets for the treatment of PCV2 infection. |
format | Online Article Text |
id | pubmed-10194317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101943172023-05-19 miR-214–5p/C1QTNF1 axis enhances PCV2 replication through promoting autophagy by targeting AKT/mTOR signaling pathway Cao, Yue Jing, Pengfei Yu, Luchen Wu, Zhengchang Gao, Song Bao, Wenbin Virus Res Article Porcine circovirus type 2 (PCV2) is the causative agent of PCV2-associated disease, which causes a relevant economic impact on the global swine industry. Accumulating data have indicated host microRNAs play essential roles in numerous virus replication of pigs, while their roles in PCV2 replication remain unclear. Herein, we demonstrated that PCV2 infection downregulated the expression of miR-214–5p in PK15 cells, and miR-214–5p promoted PCV2 replication. C1q/tumor necrosis factor-related protein 1 (C1QTNF1) was then identified as a target gene of miR-214–5p, and C1QTNF1 suppressed PCV2 replication. Interestingly, miR-214–5p/C1QTNF1 axis negatively regulated AKT/mTOR signaling, and then enhanced PCV2 replication through promoting autophagy in PK15 cells. Collectively, our findings provide insight into the mechanism of PCV2 replication and highlight miR-214–5p and C1QTNF1 as potential novel targets for the treatment of PCV2 infection. Elsevier 2022-10-24 /pmc/articles/PMC10194317/ /pubmed/36302471 http://dx.doi.org/10.1016/j.virusres.2022.198990 Text en © 2022 Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Cao, Yue Jing, Pengfei Yu, Luchen Wu, Zhengchang Gao, Song Bao, Wenbin miR-214–5p/C1QTNF1 axis enhances PCV2 replication through promoting autophagy by targeting AKT/mTOR signaling pathway |
title | miR-214–5p/C1QTNF1 axis enhances PCV2 replication through promoting autophagy by targeting AKT/mTOR signaling pathway |
title_full | miR-214–5p/C1QTNF1 axis enhances PCV2 replication through promoting autophagy by targeting AKT/mTOR signaling pathway |
title_fullStr | miR-214–5p/C1QTNF1 axis enhances PCV2 replication through promoting autophagy by targeting AKT/mTOR signaling pathway |
title_full_unstemmed | miR-214–5p/C1QTNF1 axis enhances PCV2 replication through promoting autophagy by targeting AKT/mTOR signaling pathway |
title_short | miR-214–5p/C1QTNF1 axis enhances PCV2 replication through promoting autophagy by targeting AKT/mTOR signaling pathway |
title_sort | mir-214–5p/c1qtnf1 axis enhances pcv2 replication through promoting autophagy by targeting akt/mtor signaling pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194317/ https://www.ncbi.nlm.nih.gov/pubmed/36302471 http://dx.doi.org/10.1016/j.virusres.2022.198990 |
work_keys_str_mv | AT caoyue mir2145pc1qtnf1axisenhancespcv2replicationthroughpromotingautophagybytargetingaktmtorsignalingpathway AT jingpengfei mir2145pc1qtnf1axisenhancespcv2replicationthroughpromotingautophagybytargetingaktmtorsignalingpathway AT yuluchen mir2145pc1qtnf1axisenhancespcv2replicationthroughpromotingautophagybytargetingaktmtorsignalingpathway AT wuzhengchang mir2145pc1qtnf1axisenhancespcv2replicationthroughpromotingautophagybytargetingaktmtorsignalingpathway AT gaosong mir2145pc1qtnf1axisenhancespcv2replicationthroughpromotingautophagybytargetingaktmtorsignalingpathway AT baowenbin mir2145pc1qtnf1axisenhancespcv2replicationthroughpromotingautophagybytargetingaktmtorsignalingpathway |