Cargando…
MiR-140 inhibits classical swine fever virus replication by targeting Rab25 in swine umbilical vein endothelial cells
Classical swine fever virus (CSFV) is one of the most important viral pathogens leading worldwide threats to pig industry. MicroRNAs (miRNAs) play important roles in regulating virus replication, but whether miRNAs affect CSFV infection is still poorly understood. In previous study, we identified fo...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051144/ https://www.ncbi.nlm.nih.gov/pubmed/32114898 http://dx.doi.org/10.1080/21505594.2020.1735051 |
_version_ | 1783502721037369344 |
---|---|
author | Xu, Panpan Jia, Shuangkai Wang, Kai Fan, Zhixin Zheng, Hongqing Lv, Jiangman Jiang, Yanfen Hou, Yufeng Lou, Bihao Zhou, Hongchao Zhang, Yanming Guo, Kangkang |
author_facet | Xu, Panpan Jia, Shuangkai Wang, Kai Fan, Zhixin Zheng, Hongqing Lv, Jiangman Jiang, Yanfen Hou, Yufeng Lou, Bihao Zhou, Hongchao Zhang, Yanming Guo, Kangkang |
author_sort | Xu, Panpan |
collection | PubMed |
description | Classical swine fever virus (CSFV) is one of the most important viral pathogens leading worldwide threats to pig industry. MicroRNAs (miRNAs) play important roles in regulating virus replication, but whether miRNAs affect CSFV infection is still poorly understood. In previous study, we identified four miRNAs that were down-regulated by CSFV in swine umbilical vein endothelial cells (SUVEC). In this study, miR-140, one of the most potently down-regulated genes was investigated. We found that the miRNA expression was significantly inhibited by CSFV infection. Subsequent studies revealed that miR-140 mimics significantly inhibited CSFV replication, while the inhibition of endogenous miR-140 enhanced CSFV replication. By using bioinformatics prediction, luciferase reporter system, real-time fluorescence quantitative PCR (RT-qPCR) and Western blot assays, we further demonstrated that miR-140 bind to the 3ʹ UTR of Rab25 mRNA to regulate its expression. We also analyzed the expression pattern of Rab25 in SUVECs after CSFV infection. The results showed that CSFV infection induced Rab25 expression. Finally, Rab25 was found to promote CSFV replication. In conclusion, this study demonstrated that CSFV inhibits miR-140 expression and miR-140 inhibits replication by binding to host factor Rab25. |
format | Online Article Text |
id | pubmed-7051144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-70511442020-03-10 MiR-140 inhibits classical swine fever virus replication by targeting Rab25 in swine umbilical vein endothelial cells Xu, Panpan Jia, Shuangkai Wang, Kai Fan, Zhixin Zheng, Hongqing Lv, Jiangman Jiang, Yanfen Hou, Yufeng Lou, Bihao Zhou, Hongchao Zhang, Yanming Guo, Kangkang Virulence Research Paper Classical swine fever virus (CSFV) is one of the most important viral pathogens leading worldwide threats to pig industry. MicroRNAs (miRNAs) play important roles in regulating virus replication, but whether miRNAs affect CSFV infection is still poorly understood. In previous study, we identified four miRNAs that were down-regulated by CSFV in swine umbilical vein endothelial cells (SUVEC). In this study, miR-140, one of the most potently down-regulated genes was investigated. We found that the miRNA expression was significantly inhibited by CSFV infection. Subsequent studies revealed that miR-140 mimics significantly inhibited CSFV replication, while the inhibition of endogenous miR-140 enhanced CSFV replication. By using bioinformatics prediction, luciferase reporter system, real-time fluorescence quantitative PCR (RT-qPCR) and Western blot assays, we further demonstrated that miR-140 bind to the 3ʹ UTR of Rab25 mRNA to regulate its expression. We also analyzed the expression pattern of Rab25 in SUVECs after CSFV infection. The results showed that CSFV infection induced Rab25 expression. Finally, Rab25 was found to promote CSFV replication. In conclusion, this study demonstrated that CSFV inhibits miR-140 expression and miR-140 inhibits replication by binding to host factor Rab25. Taylor & Francis 2020-02-29 /pmc/articles/PMC7051144/ /pubmed/32114898 http://dx.doi.org/10.1080/21505594.2020.1735051 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Xu, Panpan Jia, Shuangkai Wang, Kai Fan, Zhixin Zheng, Hongqing Lv, Jiangman Jiang, Yanfen Hou, Yufeng Lou, Bihao Zhou, Hongchao Zhang, Yanming Guo, Kangkang MiR-140 inhibits classical swine fever virus replication by targeting Rab25 in swine umbilical vein endothelial cells |
title | MiR-140 inhibits classical swine fever virus replication by targeting Rab25 in swine umbilical vein endothelial cells |
title_full | MiR-140 inhibits classical swine fever virus replication by targeting Rab25 in swine umbilical vein endothelial cells |
title_fullStr | MiR-140 inhibits classical swine fever virus replication by targeting Rab25 in swine umbilical vein endothelial cells |
title_full_unstemmed | MiR-140 inhibits classical swine fever virus replication by targeting Rab25 in swine umbilical vein endothelial cells |
title_short | MiR-140 inhibits classical swine fever virus replication by targeting Rab25 in swine umbilical vein endothelial cells |
title_sort | mir-140 inhibits classical swine fever virus replication by targeting rab25 in swine umbilical vein endothelial cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051144/ https://www.ncbi.nlm.nih.gov/pubmed/32114898 http://dx.doi.org/10.1080/21505594.2020.1735051 |
work_keys_str_mv | AT xupanpan mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT jiashuangkai mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT wangkai mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT fanzhixin mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT zhenghongqing mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT lvjiangman mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT jiangyanfen mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT houyufeng mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT loubihao mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT zhouhongchao mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT zhangyanming mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells AT guokangkang mir140inhibitsclassicalswinefevervirusreplicationbytargetingrab25inswineumbilicalveinendothelialcells |