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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-9627201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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