Cargando…
Cellular microRNA miR-26a suppresses replication of porcine reproductive and respiratory syndrome virus by activating innate antiviral immunity
Porcine reproductive and respiratory syndrome (PRRS) has caused large economic losses in the swine industry in recent years. Current PRRS vaccines fail to effectively prevent and control this disease. Consequently, there is a need to develop new antiviral strategies. MicroRNAs play critical roles in...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445041/ https://www.ncbi.nlm.nih.gov/pubmed/26013676 http://dx.doi.org/10.1038/srep10651 |
_version_ | 1782373227667914752 |
---|---|
author | Jia, Xiaojuan Bi, Yuhai Li, Jing Xie, Qing Yang, Hanchun Liu, Wenjun |
author_facet | Jia, Xiaojuan Bi, Yuhai Li, Jing Xie, Qing Yang, Hanchun Liu, Wenjun |
author_sort | Jia, Xiaojuan |
collection | PubMed |
description | Porcine reproductive and respiratory syndrome (PRRS) has caused large economic losses in the swine industry in recent years. Current PRRS vaccines fail to effectively prevent and control this disease. Consequently, there is a need to develop new antiviral strategies. MicroRNAs play critical roles in intricate host-pathogen interaction networks, but the involvement of miRNAs during PRRS virus (PRRSV) infection is not well understood. In this study, pretreatment with miR-26a induced a significant inhibition of PRRSV replication and remission of the cytopathic effect in MARC-145 cells, and this antiviral effect was sustained for at least 120 h. Luciferase reporter analysis showed that the PRRSV genome was not the target of miRNA-26a. Instead, RNA-seq analysis demonstrated that miR-26a significantly up-regulated innate anti-viral responses, including activating the type I interferon (IFN) signaling pathway and promoting the production of IFN-stimulated genes. These findings suggest that delivery of miR-26a may provide a potential strategy for anti-PRRSV therapies. |
format | Online Article Text |
id | pubmed-4445041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44450412015-06-01 Cellular microRNA miR-26a suppresses replication of porcine reproductive and respiratory syndrome virus by activating innate antiviral immunity Jia, Xiaojuan Bi, Yuhai Li, Jing Xie, Qing Yang, Hanchun Liu, Wenjun Sci Rep Article Porcine reproductive and respiratory syndrome (PRRS) has caused large economic losses in the swine industry in recent years. Current PRRS vaccines fail to effectively prevent and control this disease. Consequently, there is a need to develop new antiviral strategies. MicroRNAs play critical roles in intricate host-pathogen interaction networks, but the involvement of miRNAs during PRRS virus (PRRSV) infection is not well understood. In this study, pretreatment with miR-26a induced a significant inhibition of PRRSV replication and remission of the cytopathic effect in MARC-145 cells, and this antiviral effect was sustained for at least 120 h. Luciferase reporter analysis showed that the PRRSV genome was not the target of miRNA-26a. Instead, RNA-seq analysis demonstrated that miR-26a significantly up-regulated innate anti-viral responses, including activating the type I interferon (IFN) signaling pathway and promoting the production of IFN-stimulated genes. These findings suggest that delivery of miR-26a may provide a potential strategy for anti-PRRSV therapies. Nature Publishing Group 2015-05-27 /pmc/articles/PMC4445041/ /pubmed/26013676 http://dx.doi.org/10.1038/srep10651 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jia, Xiaojuan Bi, Yuhai Li, Jing Xie, Qing Yang, Hanchun Liu, Wenjun Cellular microRNA miR-26a suppresses replication of porcine reproductive and respiratory syndrome virus by activating innate antiviral immunity |
title | Cellular microRNA miR-26a suppresses replication of porcine reproductive and respiratory syndrome virus by activating innate antiviral immunity |
title_full | Cellular microRNA miR-26a suppresses replication of porcine reproductive and respiratory syndrome virus by activating innate antiviral immunity |
title_fullStr | Cellular microRNA miR-26a suppresses replication of porcine reproductive and respiratory syndrome virus by activating innate antiviral immunity |
title_full_unstemmed | Cellular microRNA miR-26a suppresses replication of porcine reproductive and respiratory syndrome virus by activating innate antiviral immunity |
title_short | Cellular microRNA miR-26a suppresses replication of porcine reproductive and respiratory syndrome virus by activating innate antiviral immunity |
title_sort | cellular microrna mir-26a suppresses replication of porcine reproductive and respiratory syndrome virus by activating innate antiviral immunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445041/ https://www.ncbi.nlm.nih.gov/pubmed/26013676 http://dx.doi.org/10.1038/srep10651 |
work_keys_str_mv | AT jiaxiaojuan cellularmicrornamir26asuppressesreplicationofporcinereproductiveandrespiratorysyndromevirusbyactivatinginnateantiviralimmunity AT biyuhai cellularmicrornamir26asuppressesreplicationofporcinereproductiveandrespiratorysyndromevirusbyactivatinginnateantiviralimmunity AT lijing cellularmicrornamir26asuppressesreplicationofporcinereproductiveandrespiratorysyndromevirusbyactivatinginnateantiviralimmunity AT xieqing cellularmicrornamir26asuppressesreplicationofporcinereproductiveandrespiratorysyndromevirusbyactivatinginnateantiviralimmunity AT yanghanchun cellularmicrornamir26asuppressesreplicationofporcinereproductiveandrespiratorysyndromevirusbyactivatinginnateantiviralimmunity AT liuwenjun cellularmicrornamir26asuppressesreplicationofporcinereproductiveandrespiratorysyndromevirusbyactivatinginnateantiviralimmunity |