MiR-125b reduces porcine reproductive and respiratory syndrome virus replication by negatively regulating the NF-κB pathway.

Porcine reproductive and respiratory syndrome virus (PRRSV) is an Arterivirus that has been devastating the swine industry worldwide since the late 1980s. To investigate the impact of cellular microRNAs (miRNAs) on the replication of PRRSV, we screened 10 highly conserved miRNAs implicated in innate...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Dang Wang, Lu Cao, Zheng Xu, Liurong Fang, Yao Zhong, Quangang Chen, Rui Luo, Huanchun Chen, Kui Li, Shaobo Xiao
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
R
Q
Acceso en línea:https://doaj.org/article/8313e8e6e6a84c0e963257215f684c70
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:8313e8e6e6a84c0e963257215f684c70
record_format dspace
spelling oai:doaj.org-article:8313e8e6e6a84c0e963257215f684c702021-11-18T07:58:18ZMiR-125b reduces porcine reproductive and respiratory syndrome virus replication by negatively regulating the NF-κB pathway.1932-620310.1371/journal.pone.0055838https://doaj.org/article/8313e8e6e6a84c0e963257215f684c702013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23409058/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Porcine reproductive and respiratory syndrome virus (PRRSV) is an Arterivirus that has been devastating the swine industry worldwide since the late 1980s. To investigate the impact of cellular microRNAs (miRNAs) on the replication of PRRSV, we screened 10 highly conserved miRNAs implicated in innate immunity or antiviral function and identified miR-125b as an inhibitor of PRRSV replication. Virus titer and western blot assays demonstrated that miR-125b reduced PRRSV replication and viral gene expression in a dose-dependent manner in both MARC-145 cell line and primary porcine alveolar macrophages. Mechanistically, miR-125b did not target the PRRSV genome. Rather, it inhibited activation of NF-κB, which we found to be required for PRRSV replication. PRRSV, in turn, down-regulated miR-125b expression post-infection to promote viral replication. Collectively, miR-125b is an antiviral host factor against PRRSV, but it is subject to manipulation by PRRSV. Our study reveals an example of manipulation of a cellular miRNA by an arterivirus to re-orchestrate host gene expression for viral propagation and sheds new light on targeting host factors to develop effective control measures for PRRS.Dang WangLu CaoZheng XuLiurong FangYao ZhongQuangang ChenRui LuoHuanchun ChenKui LiShaobo XiaoPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 2, p e55838 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Dang Wang
Lu Cao
Zheng Xu
Liurong Fang
Yao Zhong
Quangang Chen
Rui Luo
Huanchun Chen
Kui Li
Shaobo Xiao
MiR-125b reduces porcine reproductive and respiratory syndrome virus replication by negatively regulating the NF-κB pathway.
description Porcine reproductive and respiratory syndrome virus (PRRSV) is an Arterivirus that has been devastating the swine industry worldwide since the late 1980s. To investigate the impact of cellular microRNAs (miRNAs) on the replication of PRRSV, we screened 10 highly conserved miRNAs implicated in innate immunity or antiviral function and identified miR-125b as an inhibitor of PRRSV replication. Virus titer and western blot assays demonstrated that miR-125b reduced PRRSV replication and viral gene expression in a dose-dependent manner in both MARC-145 cell line and primary porcine alveolar macrophages. Mechanistically, miR-125b did not target the PRRSV genome. Rather, it inhibited activation of NF-κB, which we found to be required for PRRSV replication. PRRSV, in turn, down-regulated miR-125b expression post-infection to promote viral replication. Collectively, miR-125b is an antiviral host factor against PRRSV, but it is subject to manipulation by PRRSV. Our study reveals an example of manipulation of a cellular miRNA by an arterivirus to re-orchestrate host gene expression for viral propagation and sheds new light on targeting host factors to develop effective control measures for PRRS.
format article
author Dang Wang
Lu Cao
Zheng Xu
Liurong Fang
Yao Zhong
Quangang Chen
Rui Luo
Huanchun Chen
Kui Li
Shaobo Xiao
author_facet Dang Wang
Lu Cao
Zheng Xu
Liurong Fang
Yao Zhong
Quangang Chen
Rui Luo
Huanchun Chen
Kui Li
Shaobo Xiao
author_sort Dang Wang
title MiR-125b reduces porcine reproductive and respiratory syndrome virus replication by negatively regulating the NF-κB pathway.
title_short MiR-125b reduces porcine reproductive and respiratory syndrome virus replication by negatively regulating the NF-κB pathway.
title_full MiR-125b reduces porcine reproductive and respiratory syndrome virus replication by negatively regulating the NF-κB pathway.
title_fullStr MiR-125b reduces porcine reproductive and respiratory syndrome virus replication by negatively regulating the NF-κB pathway.
title_full_unstemmed MiR-125b reduces porcine reproductive and respiratory syndrome virus replication by negatively regulating the NF-κB pathway.
title_sort mir-125b reduces porcine reproductive and respiratory syndrome virus replication by negatively regulating the nf-κb pathway.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/8313e8e6e6a84c0e963257215f684c70
work_keys_str_mv AT dangwang mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
AT lucao mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
AT zhengxu mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
AT liurongfang mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
AT yaozhong mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
AT quangangchen mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
AT ruiluo mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
AT huanchunchen mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
AT kuili mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
AT shaoboxiao mir125breducesporcinereproductiveandrespiratorysyndromevirusreplicationbynegativelyregulatingthenfkbpathway
_version_ 1718422677898657792