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Longitudinal Profiles of Dietary and Microbial Metabolites in Formula- and Breastfed Infants

The early-life metabolome of the intestinal tract is dynamically influenced by colonization of gut microbiota which in turn is affected by nutrition, i.e. breast milk or formula. A detailed examination of fecal metabolites was performed to investigate the effect of probiotics in formula compared to...

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Autores principales: Sillner, Nina, Walker, Alesia, Lucio, Marianna, Maier, Tanja V., Bazanella, Monika, Rychlik, Michael, Haller, Dirk, Schmitt-Kopplin, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195334/
https://www.ncbi.nlm.nih.gov/pubmed/34124150
http://dx.doi.org/10.3389/fmolb.2021.660456
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author Sillner, Nina
Walker, Alesia
Lucio, Marianna
Maier, Tanja V.
Bazanella, Monika
Rychlik, Michael
Haller, Dirk
Schmitt-Kopplin, Philippe
author_facet Sillner, Nina
Walker, Alesia
Lucio, Marianna
Maier, Tanja V.
Bazanella, Monika
Rychlik, Michael
Haller, Dirk
Schmitt-Kopplin, Philippe
author_sort Sillner, Nina
collection PubMed
description The early-life metabolome of the intestinal tract is dynamically influenced by colonization of gut microbiota which in turn is affected by nutrition, i.e. breast milk or formula. A detailed examination of fecal metabolites was performed to investigate the effect of probiotics in formula compared to control formula and breast milk within the first months of life in healthy neonates. A broad metabolomics approach was conceptualized to describe fecal polar and semi-polar metabolites affected by feeding type within the first year of life. Fecal metabolomes were clearly distinct between formula- and breastfed infants, mainly originating from diet and microbial metabolism. Unsaturated fatty acids and human milk oligosaccharides were increased in breastfed, whereas Maillard products were found in feces of formula-fed children. Altered microbial metabolism was represented by bile acids and aromatic amino acid metabolites. Elevated levels of sulfated bile acids were detected in stool samples of breastfed infants, whereas secondary bile acids were increased in formula-fed infants. Microbial co-metabolism was supported by significant correlation between chenodeoxycholic or lithocholic acid and members of Clostridia. Fecal metabolites showed strong inter- and intra-individual behavior with features uniquely present in certain infants and at specific time points. Nevertheless, metabolite profiles converged at the end of the first year, coinciding with solid food introduction.
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spelling pubmed-81953342021-06-12 Longitudinal Profiles of Dietary and Microbial Metabolites in Formula- and Breastfed Infants Sillner, Nina Walker, Alesia Lucio, Marianna Maier, Tanja V. Bazanella, Monika Rychlik, Michael Haller, Dirk Schmitt-Kopplin, Philippe Front Mol Biosci Molecular Biosciences The early-life metabolome of the intestinal tract is dynamically influenced by colonization of gut microbiota which in turn is affected by nutrition, i.e. breast milk or formula. A detailed examination of fecal metabolites was performed to investigate the effect of probiotics in formula compared to control formula and breast milk within the first months of life in healthy neonates. A broad metabolomics approach was conceptualized to describe fecal polar and semi-polar metabolites affected by feeding type within the first year of life. Fecal metabolomes were clearly distinct between formula- and breastfed infants, mainly originating from diet and microbial metabolism. Unsaturated fatty acids and human milk oligosaccharides were increased in breastfed, whereas Maillard products were found in feces of formula-fed children. Altered microbial metabolism was represented by bile acids and aromatic amino acid metabolites. Elevated levels of sulfated bile acids were detected in stool samples of breastfed infants, whereas secondary bile acids were increased in formula-fed infants. Microbial co-metabolism was supported by significant correlation between chenodeoxycholic or lithocholic acid and members of Clostridia. Fecal metabolites showed strong inter- and intra-individual behavior with features uniquely present in certain infants and at specific time points. Nevertheless, metabolite profiles converged at the end of the first year, coinciding with solid food introduction. Frontiers Media S.A. 2021-05-28 /pmc/articles/PMC8195334/ /pubmed/34124150 http://dx.doi.org/10.3389/fmolb.2021.660456 Text en Copyright © 2021 Sillner, Walker, Lucio, Maier, Bazanella, Rychlik, Haller and Schmitt-Kopplin. 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 Molecular Biosciences
Sillner, Nina
Walker, Alesia
Lucio, Marianna
Maier, Tanja V.
Bazanella, Monika
Rychlik, Michael
Haller, Dirk
Schmitt-Kopplin, Philippe
Longitudinal Profiles of Dietary and Microbial Metabolites in Formula- and Breastfed Infants
title Longitudinal Profiles of Dietary and Microbial Metabolites in Formula- and Breastfed Infants
title_full Longitudinal Profiles of Dietary and Microbial Metabolites in Formula- and Breastfed Infants
title_fullStr Longitudinal Profiles of Dietary and Microbial Metabolites in Formula- and Breastfed Infants
title_full_unstemmed Longitudinal Profiles of Dietary and Microbial Metabolites in Formula- and Breastfed Infants
title_short Longitudinal Profiles of Dietary and Microbial Metabolites in Formula- and Breastfed Infants
title_sort longitudinal profiles of dietary and microbial metabolites in formula- and breastfed infants
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195334/
https://www.ncbi.nlm.nih.gov/pubmed/34124150
http://dx.doi.org/10.3389/fmolb.2021.660456
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