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A Pilot Study Exploring Temporal Development of Gut Microbiome/Metabolome in Breastfed Neonates during the First Week of Life

PURPOSE: Exclusive breastfeeding promotes gut microbial compositions associated with lower rates of metabolic and autoimmune diseases. Its cessation is implicated in increased microbiome-metabolome discordance, suggesting a vulnerability to dietary changes. Formula supplementation is common within o...

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Autores principales: Awan, Imad, Schultz, Emily, Sterrett, John D., Dawud, Lamya’a M., Kessler, Lyanna R., Schoch, Deborah, Lowry, Christopher A., Feldman-Winter, Lori, Phadtare, Sangita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025571/
https://www.ncbi.nlm.nih.gov/pubmed/36950061
http://dx.doi.org/10.5223/pghn.2023.26.2.99
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author Awan, Imad
Schultz, Emily
Sterrett, John D.
Dawud, Lamya’a M.
Kessler, Lyanna R.
Schoch, Deborah
Lowry, Christopher A.
Feldman-Winter, Lori
Phadtare, Sangita
author_facet Awan, Imad
Schultz, Emily
Sterrett, John D.
Dawud, Lamya’a M.
Kessler, Lyanna R.
Schoch, Deborah
Lowry, Christopher A.
Feldman-Winter, Lori
Phadtare, Sangita
author_sort Awan, Imad
collection PubMed
description PURPOSE: Exclusive breastfeeding promotes gut microbial compositions associated with lower rates of metabolic and autoimmune diseases. Its cessation is implicated in increased microbiome-metabolome discordance, suggesting a vulnerability to dietary changes. Formula supplementation is common within our low-income, ethnic-minority community. We studied exclusively breastfed (EBF) neonates’ early microbiome-metabolome coupling in efforts to build foundational knowledge needed to target this inequality. METHODS: Maternal surveys and stool samples from seven EBF neonates at first transitional stool (0–24 hours), discharge (30–48 hours), and at first appointment (days 3–5) were collected. Survey included demographics, feeding method, medications, medical history and tobacco and alcohol use. Stool samples were processed for 16S rRNA gene sequencing and lipid analysis by gas chromatography-mass spectrometry. Alpha and beta diversity analyses and Procrustes randomization for associations were carried out. RESULTS: Firmicutes, Proteobacteria, Bacteroidetes and Actinobacteria were the most abundant taxa. Variation in microbiome composition was greater between individuals than within (p=0.001). Palmitic, oleic, stearic, and linoleic acids were the most abundant lipids. Variation in lipid composition was greater between individuals than within (p=0.040). Multivariate composition of the metabolome, but not microbiome, correlated with time (p=0.030). Total lipids, saturated lipids, and unsaturated lipids concentrations increased over time (p=0.012, p=0.008, p=0.023). Alpha diversity did not correlate with time (p=0.403). Microbiome composition was not associated with each samples’ metabolome (p=0.450). CONCLUSION: Neonate gut microbiomes were unique to each neonate; respective metabolome profiles demonstrated generalizable temporal developments. The overall variability suggests potential interplay between influences including maternal breastmilk composition, amount consumed and living environment.
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spelling pubmed-100255712023-03-21 A Pilot Study Exploring Temporal Development of Gut Microbiome/Metabolome in Breastfed Neonates during the First Week of Life Awan, Imad Schultz, Emily Sterrett, John D. Dawud, Lamya’a M. Kessler, Lyanna R. Schoch, Deborah Lowry, Christopher A. Feldman-Winter, Lori Phadtare, Sangita Pediatr Gastroenterol Hepatol Nutr Original Article PURPOSE: Exclusive breastfeeding promotes gut microbial compositions associated with lower rates of metabolic and autoimmune diseases. Its cessation is implicated in increased microbiome-metabolome discordance, suggesting a vulnerability to dietary changes. Formula supplementation is common within our low-income, ethnic-minority community. We studied exclusively breastfed (EBF) neonates’ early microbiome-metabolome coupling in efforts to build foundational knowledge needed to target this inequality. METHODS: Maternal surveys and stool samples from seven EBF neonates at first transitional stool (0–24 hours), discharge (30–48 hours), and at first appointment (days 3–5) were collected. Survey included demographics, feeding method, medications, medical history and tobacco and alcohol use. Stool samples were processed for 16S rRNA gene sequencing and lipid analysis by gas chromatography-mass spectrometry. Alpha and beta diversity analyses and Procrustes randomization for associations were carried out. RESULTS: Firmicutes, Proteobacteria, Bacteroidetes and Actinobacteria were the most abundant taxa. Variation in microbiome composition was greater between individuals than within (p=0.001). Palmitic, oleic, stearic, and linoleic acids were the most abundant lipids. Variation in lipid composition was greater between individuals than within (p=0.040). Multivariate composition of the metabolome, but not microbiome, correlated with time (p=0.030). Total lipids, saturated lipids, and unsaturated lipids concentrations increased over time (p=0.012, p=0.008, p=0.023). Alpha diversity did not correlate with time (p=0.403). Microbiome composition was not associated with each samples’ metabolome (p=0.450). CONCLUSION: Neonate gut microbiomes were unique to each neonate; respective metabolome profiles demonstrated generalizable temporal developments. The overall variability suggests potential interplay between influences including maternal breastmilk composition, amount consumed and living environment. The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2023-03 2023-03-07 /pmc/articles/PMC10025571/ /pubmed/36950061 http://dx.doi.org/10.5223/pghn.2023.26.2.99 Text en Copyright © 2023 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Awan, Imad
Schultz, Emily
Sterrett, John D.
Dawud, Lamya’a M.
Kessler, Lyanna R.
Schoch, Deborah
Lowry, Christopher A.
Feldman-Winter, Lori
Phadtare, Sangita
A Pilot Study Exploring Temporal Development of Gut Microbiome/Metabolome in Breastfed Neonates during the First Week of Life
title A Pilot Study Exploring Temporal Development of Gut Microbiome/Metabolome in Breastfed Neonates during the First Week of Life
title_full A Pilot Study Exploring Temporal Development of Gut Microbiome/Metabolome in Breastfed Neonates during the First Week of Life
title_fullStr A Pilot Study Exploring Temporal Development of Gut Microbiome/Metabolome in Breastfed Neonates during the First Week of Life
title_full_unstemmed A Pilot Study Exploring Temporal Development of Gut Microbiome/Metabolome in Breastfed Neonates during the First Week of Life
title_short A Pilot Study Exploring Temporal Development of Gut Microbiome/Metabolome in Breastfed Neonates during the First Week of Life
title_sort pilot study exploring temporal development of gut microbiome/metabolome in breastfed neonates during the first week of life
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025571/
https://www.ncbi.nlm.nih.gov/pubmed/36950061
http://dx.doi.org/10.5223/pghn.2023.26.2.99
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