Cargando…

Maternal diet alters human milk oligosaccharide composition with implications for the milk metagenome

Human milk is the optimal nutrition source for infants, and oligosaccharides represent the third most abundant component in milk after lactose and fat. Human milk oligosaccharides (HMO) are favorable macromolecules which are, interestingly, indigestible by the infant but serve as substrates for bact...

Descripción completa

Detalles Bibliográficos
Autores principales: Seferovic, Maxim D., Mohammad, Mahmoud, Pace, Ryan M., Engevik, Melinda, Versalovic, James, Bode, Lars, Haymond, Morey, Aagaard, Kjersti M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745035/
https://www.ncbi.nlm.nih.gov/pubmed/33328537
http://dx.doi.org/10.1038/s41598-020-79022-6
_version_ 1783624534820126720
author Seferovic, Maxim D.
Mohammad, Mahmoud
Pace, Ryan M.
Engevik, Melinda
Versalovic, James
Bode, Lars
Haymond, Morey
Aagaard, Kjersti M.
author_facet Seferovic, Maxim D.
Mohammad, Mahmoud
Pace, Ryan M.
Engevik, Melinda
Versalovic, James
Bode, Lars
Haymond, Morey
Aagaard, Kjersti M.
author_sort Seferovic, Maxim D.
collection PubMed
description Human milk is the optimal nutrition source for infants, and oligosaccharides represent the third most abundant component in milk after lactose and fat. Human milk oligosaccharides (HMO) are favorable macromolecules which are, interestingly, indigestible by the infant but serve as substrates for bacteria. Hypothesizing that the maternal diet itself might influence HMO composition, we sought to directly determine the effect maternal diet on HMO and the milk bacteria. Employing a human cross-over study design, we demonstrate that distinct maternal dietary carbohydrate and energy sources preferentially alter milk concentrations of HMO, including fucosylated species. We find significant associations between the concentration of HMO-bound fucose and the abundance of fucosidase (a bacterial gene that digests fucose moieties) harbored by milk bacteria. These studies reveal a successive mechanism by which the maternal diet during lactation alters milk HMO composition, which in turn shapes the functional milk microbiome prior to infant ingestion.
format Online
Article
Text
id pubmed-7745035
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-77450352020-12-18 Maternal diet alters human milk oligosaccharide composition with implications for the milk metagenome Seferovic, Maxim D. Mohammad, Mahmoud Pace, Ryan M. Engevik, Melinda Versalovic, James Bode, Lars Haymond, Morey Aagaard, Kjersti M. Sci Rep Article Human milk is the optimal nutrition source for infants, and oligosaccharides represent the third most abundant component in milk after lactose and fat. Human milk oligosaccharides (HMO) are favorable macromolecules which are, interestingly, indigestible by the infant but serve as substrates for bacteria. Hypothesizing that the maternal diet itself might influence HMO composition, we sought to directly determine the effect maternal diet on HMO and the milk bacteria. Employing a human cross-over study design, we demonstrate that distinct maternal dietary carbohydrate and energy sources preferentially alter milk concentrations of HMO, including fucosylated species. We find significant associations between the concentration of HMO-bound fucose and the abundance of fucosidase (a bacterial gene that digests fucose moieties) harbored by milk bacteria. These studies reveal a successive mechanism by which the maternal diet during lactation alters milk HMO composition, which in turn shapes the functional milk microbiome prior to infant ingestion. Nature Publishing Group UK 2020-12-16 /pmc/articles/PMC7745035/ /pubmed/33328537 http://dx.doi.org/10.1038/s41598-020-79022-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Seferovic, Maxim D.
Mohammad, Mahmoud
Pace, Ryan M.
Engevik, Melinda
Versalovic, James
Bode, Lars
Haymond, Morey
Aagaard, Kjersti M.
Maternal diet alters human milk oligosaccharide composition with implications for the milk metagenome
title Maternal diet alters human milk oligosaccharide composition with implications for the milk metagenome
title_full Maternal diet alters human milk oligosaccharide composition with implications for the milk metagenome
title_fullStr Maternal diet alters human milk oligosaccharide composition with implications for the milk metagenome
title_full_unstemmed Maternal diet alters human milk oligosaccharide composition with implications for the milk metagenome
title_short Maternal diet alters human milk oligosaccharide composition with implications for the milk metagenome
title_sort maternal diet alters human milk oligosaccharide composition with implications for the milk metagenome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745035/
https://www.ncbi.nlm.nih.gov/pubmed/33328537
http://dx.doi.org/10.1038/s41598-020-79022-6
work_keys_str_mv AT seferovicmaximd maternaldietaltershumanmilkoligosaccharidecompositionwithimplicationsforthemilkmetagenome
AT mohammadmahmoud maternaldietaltershumanmilkoligosaccharidecompositionwithimplicationsforthemilkmetagenome
AT paceryanm maternaldietaltershumanmilkoligosaccharidecompositionwithimplicationsforthemilkmetagenome
AT engevikmelinda maternaldietaltershumanmilkoligosaccharidecompositionwithimplicationsforthemilkmetagenome
AT versalovicjames maternaldietaltershumanmilkoligosaccharidecompositionwithimplicationsforthemilkmetagenome
AT bodelars maternaldietaltershumanmilkoligosaccharidecompositionwithimplicationsforthemilkmetagenome
AT haymondmorey maternaldietaltershumanmilkoligosaccharidecompositionwithimplicationsforthemilkmetagenome
AT aagaardkjerstim maternaldietaltershumanmilkoligosaccharidecompositionwithimplicationsforthemilkmetagenome