Zika Virus-Induction of the Suppressor of Cytokine Signaling 1/3 Contributes to the Modulation of Viral Replication

Zika virus (ZIKV) is a mosquito-borne flavivirus that has emerged and caused global outbreaks since 2007. Although ZIKV proteins have been shown to suppress early anti-viral innate immune responses, little is known about the exact mechanisms. This study demonstrates that infection with either the Af...

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Main Authors: Rak-Kyun Seong, Jae Kyung Lee, Ok Sarah Shin
Format: Article
Language:English
Published: MDPI AG 2020-02-01
Series:Pathogens
Subjects:
Online Access:https://www.mdpi.com/2076-0817/9/3/163
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spelling doaj-b6c10da15e00428991b45bc0c5ca06172020-11-25T02:15:56ZengMDPI AGPathogens2076-08172020-02-019316310.3390/pathogens9030163pathogens9030163Zika Virus-Induction of the Suppressor of Cytokine Signaling 1/3 Contributes to the Modulation of Viral ReplicationRak-Kyun Seong0Jae Kyung Lee1Ok Sarah Shin2Bk21 PLUS Program, Department of Biomedical Sciences, College of Medicine, Korea University Guro Hospital, Seoul 02841, KoreaBk21 PLUS Program, Department of Biomedical Sciences, College of Medicine, Korea University Guro Hospital, Seoul 02841, KoreaBk21 PLUS Program, Department of Biomedical Sciences, College of Medicine, Korea University Guro Hospital, Seoul 02841, KoreaZika virus (ZIKV) is a mosquito-borne flavivirus that has emerged and caused global outbreaks since 2007. Although ZIKV proteins have been shown to suppress early anti-viral innate immune responses, little is known about the exact mechanisms. This study demonstrates that infection with either the African or Asian lineage of ZIKV leads to a modulated expression of suppressor of cytokine signaling (SOCS) genes encoding SOCS1 and SOCS3 in the following cell models: A549 human lung adenocarcinoma cells; JAr human choriocarcinoma cells; human neural progenitor cells. Studies of viral gene expression in response to SOCS1 or SOCS3 demonstrated that the knockdown of these SOCS proteins inhibited viral NS5 or ZIKV RNA expression, whereas overexpression resulted in an increased expression. Moreover, the overexpression of SOCS1 or SOCS3 inhibited the retinoic acid-inducible gene-I-like receptor-mediated activation of both type I and III interferon pathways. These results imply that SOCS upregulation following ZIKV infection modulates viral replication, possibly via the regulation of anti-viral innate immune responses.https://www.mdpi.com/2076-0817/9/3/163suppressor of cytokine signalingzika virusinterferonantiviral
collection DOAJ
language English
format Article
sources DOAJ
author Rak-Kyun Seong
Jae Kyung Lee
Ok Sarah Shin
spellingShingle Rak-Kyun Seong
Jae Kyung Lee
Ok Sarah Shin
Zika Virus-Induction of the Suppressor of Cytokine Signaling 1/3 Contributes to the Modulation of Viral Replication
Pathogens
suppressor of cytokine signaling
zika virus
interferon
antiviral
author_facet Rak-Kyun Seong
Jae Kyung Lee
Ok Sarah Shin
author_sort Rak-Kyun Seong
title Zika Virus-Induction of the Suppressor of Cytokine Signaling 1/3 Contributes to the Modulation of Viral Replication
title_short Zika Virus-Induction of the Suppressor of Cytokine Signaling 1/3 Contributes to the Modulation of Viral Replication
title_full Zika Virus-Induction of the Suppressor of Cytokine Signaling 1/3 Contributes to the Modulation of Viral Replication
title_fullStr Zika Virus-Induction of the Suppressor of Cytokine Signaling 1/3 Contributes to the Modulation of Viral Replication
title_full_unstemmed Zika Virus-Induction of the Suppressor of Cytokine Signaling 1/3 Contributes to the Modulation of Viral Replication
title_sort zika virus-induction of the suppressor of cytokine signaling 1/3 contributes to the modulation of viral replication
publisher MDPI AG
series Pathogens
issn 2076-0817
publishDate 2020-02-01
description Zika virus (ZIKV) is a mosquito-borne flavivirus that has emerged and caused global outbreaks since 2007. Although ZIKV proteins have been shown to suppress early anti-viral innate immune responses, little is known about the exact mechanisms. This study demonstrates that infection with either the African or Asian lineage of ZIKV leads to a modulated expression of suppressor of cytokine signaling (SOCS) genes encoding SOCS1 and SOCS3 in the following cell models: A549 human lung adenocarcinoma cells; JAr human choriocarcinoma cells; human neural progenitor cells. Studies of viral gene expression in response to SOCS1 or SOCS3 demonstrated that the knockdown of these SOCS proteins inhibited viral NS5 or ZIKV RNA expression, whereas overexpression resulted in an increased expression. Moreover, the overexpression of SOCS1 or SOCS3 inhibited the retinoic acid-inducible gene-I-like receptor-mediated activation of both type I and III interferon pathways. These results imply that SOCS upregulation following ZIKV infection modulates viral replication, possibly via the regulation of anti-viral innate immune responses.
topic suppressor of cytokine signaling
zika virus
interferon
antiviral
url https://www.mdpi.com/2076-0817/9/3/163
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AT oksarahshin zikavirusinductionofthesuppressorofcytokinesignaling13contributestothemodulationofviralreplication
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