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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...

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Autores principales: Xu, Panpan, Jia, Shuangkai, Wang, Kai, Fan, Zhixin, Zheng, Hongqing, Lv, Jiangman, Jiang, Yanfen, Hou, Yufeng, Lou, Bihao, Zhou, Hongchao, Zhang, Yanming, Guo, Kangkang
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
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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.
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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
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