Cargando…

African Swine Fever Virus Induces STAT1 and STAT2 Degradation to Counteract IFN-I Signaling

African swine fever virus (ASFV) causes a serious disease in domestic pigs and wild boars and is currently expanding worldwide. No safe and efficacious vaccines against ASFV are available, which threats the swine industry worldwide. African swine fever virus (ASFV) is a complex dsDNA virus that disp...

Descripción completa

Detalles Bibliográficos
Autores principales: Riera, Elena, Pérez-Núñez, Daniel, García-Belmonte, Raquel, Miorin, Lisa, García-Sastre, Adolfo, Revilla, Yolanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427279/
https://www.ncbi.nlm.nih.gov/pubmed/34512601
http://dx.doi.org/10.3389/fmicb.2021.722952
_version_ 1783750161551327232
author Riera, Elena
Pérez-Núñez, Daniel
García-Belmonte, Raquel
Miorin, Lisa
García-Sastre, Adolfo
Revilla, Yolanda
author_facet Riera, Elena
Pérez-Núñez, Daniel
García-Belmonte, Raquel
Miorin, Lisa
García-Sastre, Adolfo
Revilla, Yolanda
author_sort Riera, Elena
collection PubMed
description African swine fever virus (ASFV) causes a serious disease in domestic pigs and wild boars and is currently expanding worldwide. No safe and efficacious vaccines against ASFV are available, which threats the swine industry worldwide. African swine fever virus (ASFV) is a complex dsDNA virus that displays multiple mechanisms to counteract the host innate immune response, whose efficacy might determine the different degrees of virulence displayed by attenuated and virulent ASFV strains. Here we report that infection with both virulent Arm/07/CBM/c2 and attenuated NH/P68 strains prevents interferon-stimulated gene (ISG) expression in interferon (IFN)-treated cells by counteracting the JAK/STAT pathway. This inhibition results in an impaired nuclear translocation of the interferon-stimulated gene factor 3 (ISGF3) complex, as well as in the proteasome-dependent STAT2 degradation and caspase 3-dependent STAT1 cleavage. The existence of two independent mechanisms of control of the JAK/STAT pathway, suggests the importance of preventing this pathway for successful viral replication. As ASFV virulence is likely associated with the efficacy of the IFN signaling inhibitory mechanisms, a better understanding of these IFN antagonistic properties may lead to new strategies to control this devastating pig disease.
format Online
Article
Text
id pubmed-8427279
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-84272792021-09-10 African Swine Fever Virus Induces STAT1 and STAT2 Degradation to Counteract IFN-I Signaling Riera, Elena Pérez-Núñez, Daniel García-Belmonte, Raquel Miorin, Lisa García-Sastre, Adolfo Revilla, Yolanda Front Microbiol Microbiology African swine fever virus (ASFV) causes a serious disease in domestic pigs and wild boars and is currently expanding worldwide. No safe and efficacious vaccines against ASFV are available, which threats the swine industry worldwide. African swine fever virus (ASFV) is a complex dsDNA virus that displays multiple mechanisms to counteract the host innate immune response, whose efficacy might determine the different degrees of virulence displayed by attenuated and virulent ASFV strains. Here we report that infection with both virulent Arm/07/CBM/c2 and attenuated NH/P68 strains prevents interferon-stimulated gene (ISG) expression in interferon (IFN)-treated cells by counteracting the JAK/STAT pathway. This inhibition results in an impaired nuclear translocation of the interferon-stimulated gene factor 3 (ISGF3) complex, as well as in the proteasome-dependent STAT2 degradation and caspase 3-dependent STAT1 cleavage. The existence of two independent mechanisms of control of the JAK/STAT pathway, suggests the importance of preventing this pathway for successful viral replication. As ASFV virulence is likely associated with the efficacy of the IFN signaling inhibitory mechanisms, a better understanding of these IFN antagonistic properties may lead to new strategies to control this devastating pig disease. Frontiers Media S.A. 2021-08-26 /pmc/articles/PMC8427279/ /pubmed/34512601 http://dx.doi.org/10.3389/fmicb.2021.722952 Text en Copyright © 2021 Riera, Pérez-Núñez, García-Belmonte, Miorin, García-Sastre and Revilla. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Riera, Elena
Pérez-Núñez, Daniel
García-Belmonte, Raquel
Miorin, Lisa
García-Sastre, Adolfo
Revilla, Yolanda
African Swine Fever Virus Induces STAT1 and STAT2 Degradation to Counteract IFN-I Signaling
title African Swine Fever Virus Induces STAT1 and STAT2 Degradation to Counteract IFN-I Signaling
title_full African Swine Fever Virus Induces STAT1 and STAT2 Degradation to Counteract IFN-I Signaling
title_fullStr African Swine Fever Virus Induces STAT1 and STAT2 Degradation to Counteract IFN-I Signaling
title_full_unstemmed African Swine Fever Virus Induces STAT1 and STAT2 Degradation to Counteract IFN-I Signaling
title_short African Swine Fever Virus Induces STAT1 and STAT2 Degradation to Counteract IFN-I Signaling
title_sort african swine fever virus induces stat1 and stat2 degradation to counteract ifn-i signaling
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427279/
https://www.ncbi.nlm.nih.gov/pubmed/34512601
http://dx.doi.org/10.3389/fmicb.2021.722952
work_keys_str_mv AT rieraelena africanswinefevervirusinducesstat1andstat2degradationtocounteractifnisignaling
AT pereznunezdaniel africanswinefevervirusinducesstat1andstat2degradationtocounteractifnisignaling
AT garciabelmonteraquel africanswinefevervirusinducesstat1andstat2degradationtocounteractifnisignaling
AT miorinlisa africanswinefevervirusinducesstat1andstat2degradationtocounteractifnisignaling
AT garciasastreadolfo africanswinefevervirusinducesstat1andstat2degradationtocounteractifnisignaling
AT revillayolanda africanswinefevervirusinducesstat1andstat2degradationtocounteractifnisignaling