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Identification of miRNomes reveals ssc-miR-30d-R_1 as a potential therapeutic target for PRRS viral infection
Porcine reproductive and respiratory syndrome virus (PRRSV) is known to cause reproductive disorders, such as abortion, in pregnant sows as well as immunosuppressive respiratory complications, leading to severe respiratory tract infections in young pigs. In this study, an in-depth analysis of the mi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846818/ https://www.ncbi.nlm.nih.gov/pubmed/27117627 http://dx.doi.org/10.1038/srep24854 |
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author | Wang, Chengmin Zhang, Yanyu Luo, Jing Ding, Hua Liu, Shelan Amer, Said Xie, Li Lyv, Wenting Su, Wen Li, Meng Sun, Qinmiao Dai, Jiayin He, Hongxuan |
author_facet | Wang, Chengmin Zhang, Yanyu Luo, Jing Ding, Hua Liu, Shelan Amer, Said Xie, Li Lyv, Wenting Su, Wen Li, Meng Sun, Qinmiao Dai, Jiayin He, Hongxuan |
author_sort | Wang, Chengmin |
collection | PubMed |
description | Porcine reproductive and respiratory syndrome virus (PRRSV) is known to cause reproductive disorders, such as abortion, in pregnant sows as well as immunosuppressive respiratory complications, leading to severe respiratory tract infections in young pigs. In this study, an in-depth analysis of the miRNomes in mock- and virus-infected pig lungs was carried out. We found that highly expressed ssc-miR-30d-R_1 was decreased in infected lungs, and reduced levels were significantly correlated with infection by PRRSV. Moreover, ssc-miR-30d-R_1 was shown to target Toll-like receptor 4 (TLR4) and to suppress the production of immune cytokines through inhibition of the TLR4/MyD88/NF-κB pathway. ssc-miR-30d-R_1 significantly reduced viral infections and pathological changes in pig lungs in vivo. Our current study reveals the miRNomes of PRRSV-infected pig lungs and indicates that ssc-miR-30d-R_1 is potential therapeutic agent for controlling PRRSV infection. |
format | Online Article Text |
id | pubmed-4846818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48468182016-04-29 Identification of miRNomes reveals ssc-miR-30d-R_1 as a potential therapeutic target for PRRS viral infection Wang, Chengmin Zhang, Yanyu Luo, Jing Ding, Hua Liu, Shelan Amer, Said Xie, Li Lyv, Wenting Su, Wen Li, Meng Sun, Qinmiao Dai, Jiayin He, Hongxuan Sci Rep Article Porcine reproductive and respiratory syndrome virus (PRRSV) is known to cause reproductive disorders, such as abortion, in pregnant sows as well as immunosuppressive respiratory complications, leading to severe respiratory tract infections in young pigs. In this study, an in-depth analysis of the miRNomes in mock- and virus-infected pig lungs was carried out. We found that highly expressed ssc-miR-30d-R_1 was decreased in infected lungs, and reduced levels were significantly correlated with infection by PRRSV. Moreover, ssc-miR-30d-R_1 was shown to target Toll-like receptor 4 (TLR4) and to suppress the production of immune cytokines through inhibition of the TLR4/MyD88/NF-κB pathway. ssc-miR-30d-R_1 significantly reduced viral infections and pathological changes in pig lungs in vivo. Our current study reveals the miRNomes of PRRSV-infected pig lungs and indicates that ssc-miR-30d-R_1 is potential therapeutic agent for controlling PRRSV infection. Nature Publishing Group 2016-04-27 /pmc/articles/PMC4846818/ /pubmed/27117627 http://dx.doi.org/10.1038/srep24854 Text en Copyright © 2016, 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 Wang, Chengmin Zhang, Yanyu Luo, Jing Ding, Hua Liu, Shelan Amer, Said Xie, Li Lyv, Wenting Su, Wen Li, Meng Sun, Qinmiao Dai, Jiayin He, Hongxuan Identification of miRNomes reveals ssc-miR-30d-R_1 as a potential therapeutic target for PRRS viral infection |
title | Identification of miRNomes reveals ssc-miR-30d-R_1 as a potential therapeutic target for PRRS viral infection |
title_full | Identification of miRNomes reveals ssc-miR-30d-R_1 as a potential therapeutic target for PRRS viral infection |
title_fullStr | Identification of miRNomes reveals ssc-miR-30d-R_1 as a potential therapeutic target for PRRS viral infection |
title_full_unstemmed | Identification of miRNomes reveals ssc-miR-30d-R_1 as a potential therapeutic target for PRRS viral infection |
title_short | Identification of miRNomes reveals ssc-miR-30d-R_1 as a potential therapeutic target for PRRS viral infection |
title_sort | identification of mirnomes reveals ssc-mir-30d-r_1 as a potential therapeutic target for prrs viral infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846818/ https://www.ncbi.nlm.nih.gov/pubmed/27117627 http://dx.doi.org/10.1038/srep24854 |
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