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Mother’s Milk: A Purposeful Contribution to the Development of the Infant Microbiota and Immunity
Breast milk is the perfect nutrition for infants, a result of millions of years of evolution. In addition to providing a source of nutrition, breast milk contains a diverse array of microbiota and myriad biologically active components that are thought to guide the infant’s developing mucosal immune...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863526/ https://www.ncbi.nlm.nih.gov/pubmed/29599768 http://dx.doi.org/10.3389/fimmu.2018.00361 |
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author | Le Doare, Kirsty Holder, Beth Bassett, Aisha Pannaraj, Pia S. |
author_facet | Le Doare, Kirsty Holder, Beth Bassett, Aisha Pannaraj, Pia S. |
author_sort | Le Doare, Kirsty |
collection | PubMed |
description | Breast milk is the perfect nutrition for infants, a result of millions of years of evolution. In addition to providing a source of nutrition, breast milk contains a diverse array of microbiota and myriad biologically active components that are thought to guide the infant’s developing mucosal immune system. It is believed that bacteria from the mother’s intestine may translocate to breast milk and dynamically transfer to the infant. Such interplay between mother and her infant is a key to establishing a healthy infant intestinal microbiome. These intestinal bacteria protect against many respiratory and diarrheal illnesses, but are subject to environmental stresses such as antibiotic use. Orchestrating the development of the microbiota are the human milk oligosaccharides (HMOs), the synthesis of which are partially determined by the maternal genotype. HMOs are thought to play a role in preventing pathogenic bacterial adhesion though multiple mechanisms, while also providing nutrition for the microbiome. Extracellular vesicles (EVs), including exosomes, carry a diverse cargo, including mRNA, miRNA, and cytosolic and membrane-bound proteins, and are readily detectable in human breast milk. Strongly implicated in cell–cell signaling, EVs could therefore may play a further role in the development of the infant microbiome. This review considers the emerging role of breast milk microbiota, bioactive HMOs, and EVs in the establishment of the neonatal microbiome and the consequent potential for modulation of neonatal immune system development. |
format | Online Article Text |
id | pubmed-5863526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58635262018-03-29 Mother’s Milk: A Purposeful Contribution to the Development of the Infant Microbiota and Immunity Le Doare, Kirsty Holder, Beth Bassett, Aisha Pannaraj, Pia S. Front Immunol Immunology Breast milk is the perfect nutrition for infants, a result of millions of years of evolution. In addition to providing a source of nutrition, breast milk contains a diverse array of microbiota and myriad biologically active components that are thought to guide the infant’s developing mucosal immune system. It is believed that bacteria from the mother’s intestine may translocate to breast milk and dynamically transfer to the infant. Such interplay between mother and her infant is a key to establishing a healthy infant intestinal microbiome. These intestinal bacteria protect against many respiratory and diarrheal illnesses, but are subject to environmental stresses such as antibiotic use. Orchestrating the development of the microbiota are the human milk oligosaccharides (HMOs), the synthesis of which are partially determined by the maternal genotype. HMOs are thought to play a role in preventing pathogenic bacterial adhesion though multiple mechanisms, while also providing nutrition for the microbiome. Extracellular vesicles (EVs), including exosomes, carry a diverse cargo, including mRNA, miRNA, and cytosolic and membrane-bound proteins, and are readily detectable in human breast milk. Strongly implicated in cell–cell signaling, EVs could therefore may play a further role in the development of the infant microbiome. This review considers the emerging role of breast milk microbiota, bioactive HMOs, and EVs in the establishment of the neonatal microbiome and the consequent potential for modulation of neonatal immune system development. Frontiers Media S.A. 2018-02-28 /pmc/articles/PMC5863526/ /pubmed/29599768 http://dx.doi.org/10.3389/fimmu.2018.00361 Text en Copyright © 2018 Le Doare, Holder, Bassett and Pannaraj. http://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 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 Le Doare, Kirsty Holder, Beth Bassett, Aisha Pannaraj, Pia S. Mother’s Milk: A Purposeful Contribution to the Development of the Infant Microbiota and Immunity |
title | Mother’s Milk: A Purposeful Contribution to the Development of the Infant Microbiota and Immunity |
title_full | Mother’s Milk: A Purposeful Contribution to the Development of the Infant Microbiota and Immunity |
title_fullStr | Mother’s Milk: A Purposeful Contribution to the Development of the Infant Microbiota and Immunity |
title_full_unstemmed | Mother’s Milk: A Purposeful Contribution to the Development of the Infant Microbiota and Immunity |
title_short | Mother’s Milk: A Purposeful Contribution to the Development of the Infant Microbiota and Immunity |
title_sort | mother’s milk: a purposeful contribution to the development of the infant microbiota and immunity |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863526/ https://www.ncbi.nlm.nih.gov/pubmed/29599768 http://dx.doi.org/10.3389/fimmu.2018.00361 |
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