gga-miR-155 Enhances Type I Interferon Expression and Suppresses Infectious Burse Disease Virus Replication via Targeting SOCS1 and TANK

Infectious bursal disease (IBD) is an acute, highly contagious, and immunosuppressive avian disease caused by IBD virus (IBDV). MicroRNAs (miRNAs) are involved in host-pathogen interactions and innate immune response to viral infection. However, the role of miRNAs in host response to IBDV infection...

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Main Authors: Bin Wang, Mengjiao Fu, Yanan Liu, Yongqiang Wang, Xiaoqi Li, Hong Cao, Shijun J. Zheng
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fcimb.2018.00055/full
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spelling doaj-ba3cd015a2b64252b8c1100a329493252020-11-24T22:43:22ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882018-03-01810.3389/fcimb.2018.00055331244gga-miR-155 Enhances Type I Interferon Expression and Suppresses Infectious Burse Disease Virus Replication via Targeting SOCS1 and TANKBin Wang0Bin Wang1Bin Wang2Mengjiao Fu3Mengjiao Fu4Mengjiao Fu5Yanan Liu6Yanan Liu7Yanan Liu8Yongqiang Wang9Yongqiang Wang10Yongqiang Wang11Xiaoqi Li12Hong Cao13Hong Cao14Hong Cao15Shijun J. Zheng16Shijun J. Zheng17Shijun J. Zheng18State Key Laboratory of Agrobiotechnology and College of Veterinary Medicine, China Agricultural University, Beijing, ChinaKey Laboratory of Animal Epidemiology of the Ministry of Agriculture, China Agricultural University, Beijing, ChinaDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing, ChinaState Key Laboratory of Agrobiotechnology and College of Veterinary Medicine, China Agricultural University, Beijing, ChinaKey Laboratory of Animal Epidemiology of the Ministry of Agriculture, China Agricultural University, Beijing, ChinaDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing, ChinaState Key Laboratory of Agrobiotechnology and College of Veterinary Medicine, China Agricultural University, Beijing, ChinaKey Laboratory of Animal Epidemiology of the Ministry of Agriculture, China Agricultural University, Beijing, ChinaDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing, ChinaState Key Laboratory of Agrobiotechnology and College of Veterinary Medicine, China Agricultural University, Beijing, ChinaKey Laboratory of Animal Epidemiology of the Ministry of Agriculture, China Agricultural University, Beijing, ChinaDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing, ChinaDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing, ChinaState Key Laboratory of Agrobiotechnology and College of Veterinary Medicine, China Agricultural University, Beijing, ChinaKey Laboratory of Animal Epidemiology of the Ministry of Agriculture, China Agricultural University, Beijing, ChinaDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing, ChinaState Key Laboratory of Agrobiotechnology and College of Veterinary Medicine, China Agricultural University, Beijing, ChinaKey Laboratory of Animal Epidemiology of the Ministry of Agriculture, China Agricultural University, Beijing, ChinaDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing, ChinaInfectious bursal disease (IBD) is an acute, highly contagious, and immunosuppressive avian disease caused by IBD virus (IBDV). MicroRNAs (miRNAs) are involved in host-pathogen interactions and innate immune response to viral infection. However, the role of miRNAs in host response to IBDV infection is not clear. We report here that gga-miR-155 acts as an anti-virus host factor inhibiting IBDV replication. We found that transfection of DF-1 cells with gga-miR-155 suppressed IBDV replication, while blockage of the endogenous gga-miR-155 by inhibitors enhanced IBDV replication. Furthermore, our data showed that gga-miR-155 enhanced the expression of type I interferon in DF-1 cells post IBDV infection. Importantly, we found that gga-miR-155 enhanced type I interferon expression via targeting SOCS1 and TANK, two negative regulators of type I IFN signaling. These results indicate that gga-miR-155 plays a critical role in cell response to IBDV infection.http://journal.frontiersin.org/article/10.3389/fcimb.2018.00055/fullmicroRNAtype I IFNIBDVSOCSTANK
collection DOAJ
language English
format Article
sources DOAJ
author Bin Wang
Bin Wang
Bin Wang
Mengjiao Fu
Mengjiao Fu
Mengjiao Fu
Yanan Liu
Yanan Liu
Yanan Liu
Yongqiang Wang
Yongqiang Wang
Yongqiang Wang
Xiaoqi Li
Hong Cao
Hong Cao
Hong Cao
Shijun J. Zheng
Shijun J. Zheng
Shijun J. Zheng
spellingShingle Bin Wang
Bin Wang
Bin Wang
Mengjiao Fu
Mengjiao Fu
Mengjiao Fu
Yanan Liu
Yanan Liu
Yanan Liu
Yongqiang Wang
Yongqiang Wang
Yongqiang Wang
Xiaoqi Li
Hong Cao
Hong Cao
Hong Cao
Shijun J. Zheng
Shijun J. Zheng
Shijun J. Zheng
gga-miR-155 Enhances Type I Interferon Expression and Suppresses Infectious Burse Disease Virus Replication via Targeting SOCS1 and TANK
Frontiers in Cellular and Infection Microbiology
microRNA
type I IFN
IBDV
SOCS
TANK
author_facet Bin Wang
Bin Wang
Bin Wang
Mengjiao Fu
Mengjiao Fu
Mengjiao Fu
Yanan Liu
Yanan Liu
Yanan Liu
Yongqiang Wang
Yongqiang Wang
Yongqiang Wang
Xiaoqi Li
Hong Cao
Hong Cao
Hong Cao
Shijun J. Zheng
Shijun J. Zheng
Shijun J. Zheng
author_sort Bin Wang
title gga-miR-155 Enhances Type I Interferon Expression and Suppresses Infectious Burse Disease Virus Replication via Targeting SOCS1 and TANK
title_short gga-miR-155 Enhances Type I Interferon Expression and Suppresses Infectious Burse Disease Virus Replication via Targeting SOCS1 and TANK
title_full gga-miR-155 Enhances Type I Interferon Expression and Suppresses Infectious Burse Disease Virus Replication via Targeting SOCS1 and TANK
title_fullStr gga-miR-155 Enhances Type I Interferon Expression and Suppresses Infectious Burse Disease Virus Replication via Targeting SOCS1 and TANK
title_full_unstemmed gga-miR-155 Enhances Type I Interferon Expression and Suppresses Infectious Burse Disease Virus Replication via Targeting SOCS1 and TANK
title_sort gga-mir-155 enhances type i interferon expression and suppresses infectious burse disease virus replication via targeting socs1 and tank
publisher Frontiers Media S.A.
series Frontiers in Cellular and Infection Microbiology
issn 2235-2988
publishDate 2018-03-01
description Infectious bursal disease (IBD) is an acute, highly contagious, and immunosuppressive avian disease caused by IBD virus (IBDV). MicroRNAs (miRNAs) are involved in host-pathogen interactions and innate immune response to viral infection. However, the role of miRNAs in host response to IBDV infection is not clear. We report here that gga-miR-155 acts as an anti-virus host factor inhibiting IBDV replication. We found that transfection of DF-1 cells with gga-miR-155 suppressed IBDV replication, while blockage of the endogenous gga-miR-155 by inhibitors enhanced IBDV replication. Furthermore, our data showed that gga-miR-155 enhanced the expression of type I interferon in DF-1 cells post IBDV infection. Importantly, we found that gga-miR-155 enhanced type I interferon expression via targeting SOCS1 and TANK, two negative regulators of type I IFN signaling. These results indicate that gga-miR-155 plays a critical role in cell response to IBDV infection.
topic microRNA
type I IFN
IBDV
SOCS
TANK
url http://journal.frontiersin.org/article/10.3389/fcimb.2018.00055/full
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