Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2

Autores
Caminero, Alberto; McCarville, Justin L.; Galipeau, Heather J.; Deraison, Celine; Bernier, Steve P.; Constante, Marco; Rolland, Corinne; Meisel, Marlies; Murray, Joseph A.; Yu, Xuechen B.; Alaedini, Armin; Coombes, Brian K.; Bercik, Premysl; Southward, Carolyn M.; Ruf, Wolfram; Jabri, Bana; Chirdo, Fernando Gabriel; Casqueiro, Javier; Surette, Michael G.; Vergnolle, Nathalie; Verdu, Elena F.
Año de publicación
2019
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Microbe-host interactions are generally homeostatic, but when dysfunctional, they can incite food sensitivities and chronic diseases. Celiac disease (CeD) is a food sensitivity characterized by a breakdown of oral tolerance to gluten proteins in genetically predisposed individuals, although the underlying mechanisms are incompletely understood. Here we show that duodenal biopsies from patients with active CeD have increased proteolytic activity against gluten substrates that correlates with increased Proteobacteria abundance, including Pseudomonas. Using Pseudomonas aeruginosa producing elastase as a model, we show gluten-independent, PAR-2 mediated upregulation of inflammatory pathways in C57BL/6 mice without villus blunting. In mice expressing CeD risk genes, P. aeruginosa elastase synergizes with gluten to induce more severe inflammation that is associated with moderate villus blunting. These results demonstrate that proteases expressed by opportunistic pathogens impact host immune responses that are relevant to the development of food sensitivities, independently of the trigger antigen.
Instituto de Estudios Inmunológicos y Fisiopatológicos
Materia
Biología
Proteases
Microbe-host interactions
Food sensitivities
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/107005

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repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2Caminero, AlbertoMcCarville, Justin L.Galipeau, Heather J.Deraison, CelineBernier, Steve P.Constante, MarcoRolland, CorinneMeisel, MarliesMurray, Joseph A.Yu, Xuechen B.Alaedini, ArminCoombes, Brian K.Bercik, PremyslSouthward, Carolyn M.Ruf, WolframJabri, BanaChirdo, Fernando GabrielCasqueiro, JavierSurette, Michael G.Vergnolle, NathalieVerdu, Elena F.BiologíaProteasesMicrobe-host interactionsFood sensitivitiesMicrobe-host interactions are generally homeostatic, but when dysfunctional, they can incite food sensitivities and chronic diseases. Celiac disease (CeD) is a food sensitivity characterized by a breakdown of oral tolerance to gluten proteins in genetically predisposed individuals, although the underlying mechanisms are incompletely understood. Here we show that duodenal biopsies from patients with active CeD have increased proteolytic activity against gluten substrates that correlates with increased Proteobacteria abundance, including Pseudomonas. Using Pseudomonas aeruginosa producing elastase as a model, we show gluten-independent, PAR-2 mediated upregulation of inflammatory pathways in C57BL/6 mice without villus blunting. In mice expressing CeD risk genes, P. aeruginosa elastase synergizes with gluten to induce more severe inflammation that is associated with moderate villus blunting. These results demonstrate that proteases expressed by opportunistic pathogens impact host immune responses that are relevant to the development of food sensitivities, independently of the trigger antigen.Instituto de Estudios Inmunológicos y Fisiopatológicos2019info: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/10915/107005enginfo:eu-repo/semantics/altIdentifier/url/http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC6416356&blobtype=pdfinfo:eu-repo/semantics/altIdentifier/issn/2041-1723info:eu-repo/semantics/altIdentifier/pmid/30867416info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-019-09037-9info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:15:47Zoai:sedici.unlp.edu.ar:10915/107005Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:15:47.722SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2
title Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2
spellingShingle Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2
Caminero, Alberto
Biología
Proteases
Microbe-host interactions
Food sensitivities
title_short Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2
title_full Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2
title_fullStr Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2
title_full_unstemmed Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2
title_sort Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2
dc.creator.none.fl_str_mv Caminero, Alberto
McCarville, Justin L.
Galipeau, Heather J.
Deraison, Celine
Bernier, Steve P.
Constante, Marco
Rolland, Corinne
Meisel, Marlies
Murray, Joseph A.
Yu, Xuechen B.
Alaedini, Armin
Coombes, Brian K.
Bercik, Premysl
Southward, Carolyn M.
Ruf, Wolfram
Jabri, Bana
Chirdo, Fernando Gabriel
Casqueiro, Javier
Surette, Michael G.
Vergnolle, Nathalie
Verdu, Elena F.
author Caminero, Alberto
author_facet Caminero, Alberto
McCarville, Justin L.
Galipeau, Heather J.
Deraison, Celine
Bernier, Steve P.
Constante, Marco
Rolland, Corinne
Meisel, Marlies
Murray, Joseph A.
Yu, Xuechen B.
Alaedini, Armin
Coombes, Brian K.
Bercik, Premysl
Southward, Carolyn M.
Ruf, Wolfram
Jabri, Bana
Chirdo, Fernando Gabriel
Casqueiro, Javier
Surette, Michael G.
Vergnolle, Nathalie
Verdu, Elena F.
author_role author
author2 McCarville, Justin L.
Galipeau, Heather J.
Deraison, Celine
Bernier, Steve P.
Constante, Marco
Rolland, Corinne
Meisel, Marlies
Murray, Joseph A.
Yu, Xuechen B.
Alaedini, Armin
Coombes, Brian K.
Bercik, Premysl
Southward, Carolyn M.
Ruf, Wolfram
Jabri, Bana
Chirdo, Fernando Gabriel
Casqueiro, Javier
Surette, Michael G.
Vergnolle, Nathalie
Verdu, Elena F.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Biología
Proteases
Microbe-host interactions
Food sensitivities
topic Biología
Proteases
Microbe-host interactions
Food sensitivities
dc.description.none.fl_txt_mv Microbe-host interactions are generally homeostatic, but when dysfunctional, they can incite food sensitivities and chronic diseases. Celiac disease (CeD) is a food sensitivity characterized by a breakdown of oral tolerance to gluten proteins in genetically predisposed individuals, although the underlying mechanisms are incompletely understood. Here we show that duodenal biopsies from patients with active CeD have increased proteolytic activity against gluten substrates that correlates with increased Proteobacteria abundance, including Pseudomonas. Using Pseudomonas aeruginosa producing elastase as a model, we show gluten-independent, PAR-2 mediated upregulation of inflammatory pathways in C57BL/6 mice without villus blunting. In mice expressing CeD risk genes, P. aeruginosa elastase synergizes with gluten to induce more severe inflammation that is associated with moderate villus blunting. These results demonstrate that proteases expressed by opportunistic pathogens impact host immune responses that are relevant to the development of food sensitivities, independently of the trigger antigen.
Instituto de Estudios Inmunológicos y Fisiopatológicos
description Microbe-host interactions are generally homeostatic, but when dysfunctional, they can incite food sensitivities and chronic diseases. Celiac disease (CeD) is a food sensitivity characterized by a breakdown of oral tolerance to gluten proteins in genetically predisposed individuals, although the underlying mechanisms are incompletely understood. Here we show that duodenal biopsies from patients with active CeD have increased proteolytic activity against gluten substrates that correlates with increased Proteobacteria abundance, including Pseudomonas. Using Pseudomonas aeruginosa producing elastase as a model, we show gluten-independent, PAR-2 mediated upregulation of inflammatory pathways in C57BL/6 mice without villus blunting. In mice expressing CeD risk genes, P. aeruginosa elastase synergizes with gluten to induce more severe inflammation that is associated with moderate villus blunting. These results demonstrate that proteases expressed by opportunistic pathogens impact host immune responses that are relevant to the development of food sensitivities, independently of the trigger antigen.
publishDate 2019
dc.date.none.fl_str_mv 2019
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/107005
url http://sedici.unlp.edu.ar/handle/10915/107005
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC6416356&blobtype=pdf
info:eu-repo/semantics/altIdentifier/issn/2041-1723
info:eu-repo/semantics/altIdentifier/pmid/30867416
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-019-09037-9
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 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)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
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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