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Dietary phytate primes epithelial antibacterial immunity in the intestine

Although diet has long been associated with susceptibility to infection, the dietary components that regulate host defense remain poorly understood. Here, we demonstrate that consuming rice bran decreases susceptibility to intestinal infection with Citrobacter rodentium, a murine pathogen that is si...

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Autores principales: Hashimoto-Hill, Seika, Colapietro, Luisa, Woo, Vivienne, Antonacci, Simona, Whitt, Jordan, Engleman, Laura, Alenghat, Theresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627201/
https://www.ncbi.nlm.nih.gov/pubmed/36341403
http://dx.doi.org/10.3389/fimmu.2022.952994
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author Hashimoto-Hill, Seika
Colapietro, Luisa
Woo, Vivienne
Antonacci, Simona
Whitt, Jordan
Engleman, Laura
Alenghat, Theresa
author_facet Hashimoto-Hill, Seika
Colapietro, Luisa
Woo, Vivienne
Antonacci, Simona
Whitt, Jordan
Engleman, Laura
Alenghat, Theresa
author_sort Hashimoto-Hill, Seika
collection PubMed
description Although diet has long been associated with susceptibility to infection, the dietary components that regulate host defense remain poorly understood. Here, we demonstrate that consuming rice bran decreases susceptibility to intestinal infection with Citrobacter rodentium, a murine pathogen that is similar to enteropathogenic E. coli infection in humans. Rice bran naturally contains high levels of the substance phytate. Interestingly, phytate supplementation also protected against intestinal infection, and enzymatic metabolism of phytate by commensal bacteria was necessary for phytate-induced host defense. Mechanistically, phytate consumption induced mammalian intestinal epithelial expression of STAT3-regulated antimicrobial pathways and increased phosphorylated STAT3, suggesting that dietary phytate promotes innate defense through epithelial STAT3 activation. Further, phytate regulation of epithelial STAT3 was mediated by the microbiota-sensitive enzyme histone deacetylase 3 (HDAC3). Collectively, these data demonstrate that metabolism of dietary phytate by microbiota decreases intestinal infection and suggests that consuming bran and other phytate-enriched foods may represent an effective dietary strategy for priming host immunity.
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spelling pubmed-96272012022-11-03 Dietary phytate primes epithelial antibacterial immunity in the intestine Hashimoto-Hill, Seika Colapietro, Luisa Woo, Vivienne Antonacci, Simona Whitt, Jordan Engleman, Laura Alenghat, Theresa Front Immunol Immunology Although diet has long been associated with susceptibility to infection, the dietary components that regulate host defense remain poorly understood. Here, we demonstrate that consuming rice bran decreases susceptibility to intestinal infection with Citrobacter rodentium, a murine pathogen that is similar to enteropathogenic E. coli infection in humans. Rice bran naturally contains high levels of the substance phytate. Interestingly, phytate supplementation also protected against intestinal infection, and enzymatic metabolism of phytate by commensal bacteria was necessary for phytate-induced host defense. Mechanistically, phytate consumption induced mammalian intestinal epithelial expression of STAT3-regulated antimicrobial pathways and increased phosphorylated STAT3, suggesting that dietary phytate promotes innate defense through epithelial STAT3 activation. Further, phytate regulation of epithelial STAT3 was mediated by the microbiota-sensitive enzyme histone deacetylase 3 (HDAC3). Collectively, these data demonstrate that metabolism of dietary phytate by microbiota decreases intestinal infection and suggests that consuming bran and other phytate-enriched foods may represent an effective dietary strategy for priming host immunity. Frontiers Media S.A. 2022-10-19 /pmc/articles/PMC9627201/ /pubmed/36341403 http://dx.doi.org/10.3389/fimmu.2022.952994 Text en Copyright © 2022 Hashimoto-Hill, Colapietro, Woo, Antonacci, Whitt, Engleman and Alenghat 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 Immunology
Hashimoto-Hill, Seika
Colapietro, Luisa
Woo, Vivienne
Antonacci, Simona
Whitt, Jordan
Engleman, Laura
Alenghat, Theresa
Dietary phytate primes epithelial antibacterial immunity in the intestine
title Dietary phytate primes epithelial antibacterial immunity in the intestine
title_full Dietary phytate primes epithelial antibacterial immunity in the intestine
title_fullStr Dietary phytate primes epithelial antibacterial immunity in the intestine
title_full_unstemmed Dietary phytate primes epithelial antibacterial immunity in the intestine
title_short Dietary phytate primes epithelial antibacterial immunity in the intestine
title_sort dietary phytate primes epithelial antibacterial immunity in the intestine
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627201/
https://www.ncbi.nlm.nih.gov/pubmed/36341403
http://dx.doi.org/10.3389/fimmu.2022.952994
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