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Exclusively Breastfed Infant Microbiota Develops over Time and Is Associated with Human Milk Oligosaccharide Intakes

Temporal development of maternal and infant microbiomes during early life impacts short- and long-term infant health. This study aimed to characterize bacterial dynamics within maternal faecal, human milk (HM), infant oral, and infant faecal samples during the exclusive breastfeeding period and to d...

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Autores principales: Cheema, Ali Sadiq, Trevenen, Michelle Louise, Turlach, Berwin Ashoka, Furst, Annalee June, Roman, Ana Sophia, Bode, Lars, Gridneva, Zoya, Lai, Ching Tat, Stinson, Lisa Faye, Payne, Matthew Scott, Geddes, Donna Tracy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910998/
https://www.ncbi.nlm.nih.gov/pubmed/35269946
http://dx.doi.org/10.3390/ijms23052804
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author Cheema, Ali Sadiq
Trevenen, Michelle Louise
Turlach, Berwin Ashoka
Furst, Annalee June
Roman, Ana Sophia
Bode, Lars
Gridneva, Zoya
Lai, Ching Tat
Stinson, Lisa Faye
Payne, Matthew Scott
Geddes, Donna Tracy
author_facet Cheema, Ali Sadiq
Trevenen, Michelle Louise
Turlach, Berwin Ashoka
Furst, Annalee June
Roman, Ana Sophia
Bode, Lars
Gridneva, Zoya
Lai, Ching Tat
Stinson, Lisa Faye
Payne, Matthew Scott
Geddes, Donna Tracy
author_sort Cheema, Ali Sadiq
collection PubMed
description Temporal development of maternal and infant microbiomes during early life impacts short- and long-term infant health. This study aimed to characterize bacterial dynamics within maternal faecal, human milk (HM), infant oral, and infant faecal samples during the exclusive breastfeeding period and to document associations between human milk oligosaccharide (HMO) intakes and infant oral and faecal bacterial profiles. Maternal and infant samples (n = 10) were collected at 2–5, 30, 60, 90 and 120 days postpartum and the full-length 16S ribosomal RNA (rRNA) gene was sequenced. Nineteen HMOs were quantitated using high-performance liquid chromatography. Bacterial profiles were unique to each sample type and changed significantly over time, with a large degree of intra- and inter-individual variation in all sample types. Beta diversity was stable over time within infant faecal, maternal faecal and HM samples, however, the infant oral microbiota at day 2–5 significantly differed from all other time points (all p < 0.02). HMO concentrations and intakes significantly differed over time, and HMO intakes showed differential associations with taxa observed in infant oral and faecal samples. The direct clinical relevance of this, however, is unknown. Regardless, future studies should account for intakes of HMOs when modelling the impact of HM on infant growth, as it may have implications for infant microbiota development.
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spelling pubmed-89109982022-03-11 Exclusively Breastfed Infant Microbiota Develops over Time and Is Associated with Human Milk Oligosaccharide Intakes Cheema, Ali Sadiq Trevenen, Michelle Louise Turlach, Berwin Ashoka Furst, Annalee June Roman, Ana Sophia Bode, Lars Gridneva, Zoya Lai, Ching Tat Stinson, Lisa Faye Payne, Matthew Scott Geddes, Donna Tracy Int J Mol Sci Article Temporal development of maternal and infant microbiomes during early life impacts short- and long-term infant health. This study aimed to characterize bacterial dynamics within maternal faecal, human milk (HM), infant oral, and infant faecal samples during the exclusive breastfeeding period and to document associations between human milk oligosaccharide (HMO) intakes and infant oral and faecal bacterial profiles. Maternal and infant samples (n = 10) were collected at 2–5, 30, 60, 90 and 120 days postpartum and the full-length 16S ribosomal RNA (rRNA) gene was sequenced. Nineteen HMOs were quantitated using high-performance liquid chromatography. Bacterial profiles were unique to each sample type and changed significantly over time, with a large degree of intra- and inter-individual variation in all sample types. Beta diversity was stable over time within infant faecal, maternal faecal and HM samples, however, the infant oral microbiota at day 2–5 significantly differed from all other time points (all p < 0.02). HMO concentrations and intakes significantly differed over time, and HMO intakes showed differential associations with taxa observed in infant oral and faecal samples. The direct clinical relevance of this, however, is unknown. Regardless, future studies should account for intakes of HMOs when modelling the impact of HM on infant growth, as it may have implications for infant microbiota development. MDPI 2022-03-03 /pmc/articles/PMC8910998/ /pubmed/35269946 http://dx.doi.org/10.3390/ijms23052804 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cheema, Ali Sadiq
Trevenen, Michelle Louise
Turlach, Berwin Ashoka
Furst, Annalee June
Roman, Ana Sophia
Bode, Lars
Gridneva, Zoya
Lai, Ching Tat
Stinson, Lisa Faye
Payne, Matthew Scott
Geddes, Donna Tracy
Exclusively Breastfed Infant Microbiota Develops over Time and Is Associated with Human Milk Oligosaccharide Intakes
title Exclusively Breastfed Infant Microbiota Develops over Time and Is Associated with Human Milk Oligosaccharide Intakes
title_full Exclusively Breastfed Infant Microbiota Develops over Time and Is Associated with Human Milk Oligosaccharide Intakes
title_fullStr Exclusively Breastfed Infant Microbiota Develops over Time and Is Associated with Human Milk Oligosaccharide Intakes
title_full_unstemmed Exclusively Breastfed Infant Microbiota Develops over Time and Is Associated with Human Milk Oligosaccharide Intakes
title_short Exclusively Breastfed Infant Microbiota Develops over Time and Is Associated with Human Milk Oligosaccharide Intakes
title_sort exclusively breastfed infant microbiota develops over time and is associated with human milk oligosaccharide intakes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910998/
https://www.ncbi.nlm.nih.gov/pubmed/35269946
http://dx.doi.org/10.3390/ijms23052804
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