Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replication

Autores
Colina, Santiago Emanuel; Williman, Macarena Marta; Serena, María Soledad; Echeverría, María Gabriela; Metz, Germán Ernesto
Año de publicación
2025
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The perturbation of ER homeostasis by viral infection gives rise to the unfolded protein response (UPR), characterized by the activation of three signaling pathways. PERK, IRE1, and ATF6 have been identified as the primary mediators responsible for restoring homeostasis or leading to apoptosis in response to stress. Alphaarterivirus equid, known as equine arteritis virus (EAV), is a RNA virus with importance in the equine industry that could persist in semen and lead to abortions in pregnant mares. The present article explores the consequences of in vitro infection with the EAV Bucyrus strain on UPR. Employing RT-PCR, qPCR and Western blot, our investigation has revealed the activation of PERK and IRE1α pathways, whilst ATF6 has been suppressed. Furthermore, the p38α MAPK, caspase-12, and CHOP genes were found to be upregulated, demonstrating the induction of apoptosis. Finally, in the inhibition experiments, the PERK pathway was found to be implicated in the modulation of viral replication in the initial phases of infection. Conversely, the IRE1α pathway was identified as the predominant UPR pathway in EAV replication, as evidenced by the complete inhibition of replication observed in these experiments. Consequently, the further exploration of this UPR pathway is necessary to determine whether it can effectively suppress EAV replication.
Facultad de Ciencias Veterinarias
Materia
Ciencias Veterinarias
RNA virus
Equine arteritis virus
ER stress
PERK
IRE1α
Apoptosis
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/186522

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network_name_str SEDICI (UNLP)
spelling Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replicationColina, Santiago EmanuelWilliman, Macarena MartaSerena, María SoledadEcheverría, María GabrielaMetz, Germán ErnestoCiencias VeterinariasRNA virusEquine arteritis virusER stressPERKIRE1αApoptosisThe perturbation of ER homeostasis by viral infection gives rise to the unfolded protein response (UPR), characterized by the activation of three signaling pathways. PERK, IRE1, and ATF6 have been identified as the primary mediators responsible for restoring homeostasis or leading to apoptosis in response to stress. Alphaarterivirus equid, known as equine arteritis virus (EAV), is a RNA virus with importance in the equine industry that could persist in semen and lead to abortions in pregnant mares. The present article explores the consequences of in vitro infection with the EAV Bucyrus strain on UPR. Employing RT-PCR, qPCR and Western blot, our investigation has revealed the activation of PERK and IRE1α pathways, whilst ATF6 has been suppressed. Furthermore, the p38α MAPK, caspase-12, and CHOP genes were found to be upregulated, demonstrating the induction of apoptosis. Finally, in the inhibition experiments, the PERK pathway was found to be implicated in the modulation of viral replication in the initial phases of infection. Conversely, the IRE1α pathway was identified as the predominant UPR pathway in EAV replication, as evidenced by the complete inhibition of replication observed in these experiments. Consequently, the further exploration of this UPR pathway is necessary to determine whether it can effectively suppress EAV replication.Facultad de Ciencias Veterinarias2025-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/186522enginfo:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/1999-4915/17/10/1301info:eu-repo/semantics/altIdentifier/issn/1999-4915info:eu-repo/semantics/altIdentifier/doi/10.3390/v17101301info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-11-12T11:15:32Zoai:sedici.unlp.edu.ar:10915/186522Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-11-12 11:15:33.248SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replication
title Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replication
spellingShingle Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replication
Colina, Santiago Emanuel
Ciencias Veterinarias
RNA virus
Equine arteritis virus
ER stress
PERK
IRE1α
Apoptosis
title_short Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replication
title_full Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replication
title_fullStr Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replication
title_full_unstemmed Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replication
title_sort Role of unfolded protein response in the apoptosis induced by alphaarterivirus : IRE1α as an essential pathway for In vitro replication
dc.creator.none.fl_str_mv Colina, Santiago Emanuel
Williman, Macarena Marta
Serena, María Soledad
Echeverría, María Gabriela
Metz, Germán Ernesto
author Colina, Santiago Emanuel
author_facet Colina, Santiago Emanuel
Williman, Macarena Marta
Serena, María Soledad
Echeverría, María Gabriela
Metz, Germán Ernesto
author_role author
author2 Williman, Macarena Marta
Serena, María Soledad
Echeverría, María Gabriela
Metz, Germán Ernesto
author2_role author
author
author
author
dc.subject.none.fl_str_mv Ciencias Veterinarias
RNA virus
Equine arteritis virus
ER stress
PERK
IRE1α
Apoptosis
topic Ciencias Veterinarias
RNA virus
Equine arteritis virus
ER stress
PERK
IRE1α
Apoptosis
dc.description.none.fl_txt_mv The perturbation of ER homeostasis by viral infection gives rise to the unfolded protein response (UPR), characterized by the activation of three signaling pathways. PERK, IRE1, and ATF6 have been identified as the primary mediators responsible for restoring homeostasis or leading to apoptosis in response to stress. Alphaarterivirus equid, known as equine arteritis virus (EAV), is a RNA virus with importance in the equine industry that could persist in semen and lead to abortions in pregnant mares. The present article explores the consequences of in vitro infection with the EAV Bucyrus strain on UPR. Employing RT-PCR, qPCR and Western blot, our investigation has revealed the activation of PERK and IRE1α pathways, whilst ATF6 has been suppressed. Furthermore, the p38α MAPK, caspase-12, and CHOP genes were found to be upregulated, demonstrating the induction of apoptosis. Finally, in the inhibition experiments, the PERK pathway was found to be implicated in the modulation of viral replication in the initial phases of infection. Conversely, the IRE1α pathway was identified as the predominant UPR pathway in EAV replication, as evidenced by the complete inhibition of replication observed in these experiments. Consequently, the further exploration of this UPR pathway is necessary to determine whether it can effectively suppress EAV replication.
Facultad de Ciencias Veterinarias
description The perturbation of ER homeostasis by viral infection gives rise to the unfolded protein response (UPR), characterized by the activation of three signaling pathways. PERK, IRE1, and ATF6 have been identified as the primary mediators responsible for restoring homeostasis or leading to apoptosis in response to stress. Alphaarterivirus equid, known as equine arteritis virus (EAV), is a RNA virus with importance in the equine industry that could persist in semen and lead to abortions in pregnant mares. The present article explores the consequences of in vitro infection with the EAV Bucyrus strain on UPR. Employing RT-PCR, qPCR and Western blot, our investigation has revealed the activation of PERK and IRE1α pathways, whilst ATF6 has been suppressed. Furthermore, the p38α MAPK, caspase-12, and CHOP genes were found to be upregulated, demonstrating the induction of apoptosis. Finally, in the inhibition experiments, the PERK pathway was found to be implicated in the modulation of viral replication in the initial phases of infection. Conversely, the IRE1α pathway was identified as the predominant UPR pathway in EAV replication, as evidenced by the complete inhibition of replication observed in these experiments. Consequently, the further exploration of this UPR pathway is necessary to determine whether it can effectively suppress EAV replication.
publishDate 2025
dc.date.none.fl_str_mv 2025-09
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/186522
url http://sedici.unlp.edu.ar/handle/10915/186522
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/1999-4915/17/10/1301
info:eu-repo/semantics/altIdentifier/issn/1999-4915
info:eu-repo/semantics/altIdentifier/doi/10.3390/v17101301
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
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institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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