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Maternal Supplementation of Food Ingredient (Prebiotic) or Food Contaminant (Mycotoxin) Influences Mucosal Immune System in Piglets

The early life period is crucial for the maturation of the intestinal barrier, its immune system, and a life-long beneficial host–microbiota interaction. The study aims to assess the impact of a beneficial dietary (short-chain fructooligosaccharides, scFOS) supplementation vs. a detrimental dietary...

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Autores principales: Ferret-Bernard, Stéphanie, Le Normand, Laurence, Romé, Véronique, Le Bourgot, Cindy, Seeboth, Julie, Savary, Gérard, Laurent, Fabrice, Le Huërou-Luron, Isabelle, Guzylack-Piriou, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400953/
https://www.ncbi.nlm.nih.gov/pubmed/32708852
http://dx.doi.org/10.3390/nu12072115
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author Ferret-Bernard, Stéphanie
Le Normand, Laurence
Romé, Véronique
Le Bourgot, Cindy
Seeboth, Julie
Savary, Gérard
Laurent, Fabrice
Le Huërou-Luron, Isabelle
Guzylack-Piriou, Laurence
author_facet Ferret-Bernard, Stéphanie
Le Normand, Laurence
Romé, Véronique
Le Bourgot, Cindy
Seeboth, Julie
Savary, Gérard
Laurent, Fabrice
Le Huërou-Luron, Isabelle
Guzylack-Piriou, Laurence
author_sort Ferret-Bernard, Stéphanie
collection PubMed
description The early life period is crucial for the maturation of the intestinal barrier, its immune system, and a life-long beneficial host–microbiota interaction. The study aims to assess the impact of a beneficial dietary (short-chain fructooligosaccharides, scFOS) supplementation vs. a detrimental dietary environment (such as mycotoxin deoxynivalenol, DON) on offspring intestinal immune system developmental profiles. Sows were given scFOS-supplemented or DON-contaminated diets during the last 4 weeks of gestation, whereas force-feeding piglets with DON was performed during the first week of offspring life. Intestinal antigen-presenting cell (APC) subset frequency was analyzed by flow cytometry in the Peyer’s patches and in lamina propria and the responsiveness of intestinal explants to toll-like receptor (TLR) ligands was performed using ELISA and qRT-PCR from post-natal day (PND) 10 until PND90. Perinatal exposure with scFOS did not affect the ontogenesis of APC. While it early induced inflammatory responses in piglets, scFOS further promoted the T regulatory response after TLR activation. Sow and piglet DON contamination decreased CD16+ MHCII+ APC at PND10 in lamina propria associated with IFNγ inflammation and impairment of Treg response. Our study demonstrated that maternal prebiotic supplementation and mycotoxin contamination can modulate the mucosal immune system responsiveness of offspring through different pathways.
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spelling pubmed-74009532020-08-07 Maternal Supplementation of Food Ingredient (Prebiotic) or Food Contaminant (Mycotoxin) Influences Mucosal Immune System in Piglets Ferret-Bernard, Stéphanie Le Normand, Laurence Romé, Véronique Le Bourgot, Cindy Seeboth, Julie Savary, Gérard Laurent, Fabrice Le Huërou-Luron, Isabelle Guzylack-Piriou, Laurence Nutrients Article The early life period is crucial for the maturation of the intestinal barrier, its immune system, and a life-long beneficial host–microbiota interaction. The study aims to assess the impact of a beneficial dietary (short-chain fructooligosaccharides, scFOS) supplementation vs. a detrimental dietary environment (such as mycotoxin deoxynivalenol, DON) on offspring intestinal immune system developmental profiles. Sows were given scFOS-supplemented or DON-contaminated diets during the last 4 weeks of gestation, whereas force-feeding piglets with DON was performed during the first week of offspring life. Intestinal antigen-presenting cell (APC) subset frequency was analyzed by flow cytometry in the Peyer’s patches and in lamina propria and the responsiveness of intestinal explants to toll-like receptor (TLR) ligands was performed using ELISA and qRT-PCR from post-natal day (PND) 10 until PND90. Perinatal exposure with scFOS did not affect the ontogenesis of APC. While it early induced inflammatory responses in piglets, scFOS further promoted the T regulatory response after TLR activation. Sow and piglet DON contamination decreased CD16+ MHCII+ APC at PND10 in lamina propria associated with IFNγ inflammation and impairment of Treg response. Our study demonstrated that maternal prebiotic supplementation and mycotoxin contamination can modulate the mucosal immune system responsiveness of offspring through different pathways. MDPI 2020-07-17 /pmc/articles/PMC7400953/ /pubmed/32708852 http://dx.doi.org/10.3390/nu12072115 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ferret-Bernard, Stéphanie
Le Normand, Laurence
Romé, Véronique
Le Bourgot, Cindy
Seeboth, Julie
Savary, Gérard
Laurent, Fabrice
Le Huërou-Luron, Isabelle
Guzylack-Piriou, Laurence
Maternal Supplementation of Food Ingredient (Prebiotic) or Food Contaminant (Mycotoxin) Influences Mucosal Immune System in Piglets
title Maternal Supplementation of Food Ingredient (Prebiotic) or Food Contaminant (Mycotoxin) Influences Mucosal Immune System in Piglets
title_full Maternal Supplementation of Food Ingredient (Prebiotic) or Food Contaminant (Mycotoxin) Influences Mucosal Immune System in Piglets
title_fullStr Maternal Supplementation of Food Ingredient (Prebiotic) or Food Contaminant (Mycotoxin) Influences Mucosal Immune System in Piglets
title_full_unstemmed Maternal Supplementation of Food Ingredient (Prebiotic) or Food Contaminant (Mycotoxin) Influences Mucosal Immune System in Piglets
title_short Maternal Supplementation of Food Ingredient (Prebiotic) or Food Contaminant (Mycotoxin) Influences Mucosal Immune System in Piglets
title_sort maternal supplementation of food ingredient (prebiotic) or food contaminant (mycotoxin) influences mucosal immune system in piglets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400953/
https://www.ncbi.nlm.nih.gov/pubmed/32708852
http://dx.doi.org/10.3390/nu12072115
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