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Antibiotics and the developing intestinal microbiome, metabolome and inflammatory environment in a randomized trial of preterm infants

Antibiotic use in neonates can have detrimental effects on the developing gut microbiome, increasing the risk of morbidity. A majority of preterm neonates receive antibiotics after birth without clear evidence to guide this practice. Here microbiome, metabolomic, and immune marker results from the r...

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Autores principales: Russell, Jordan T., Lauren Ruoss, J., de la Cruz, Diomel, Li, Nan, Bazacliu, Catalina, Patton, Laura, McKinley, Kelley Lobean, Garrett, Timothy J., Polin, Richard A., Triplett, Eric W., Neu, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820285/
https://www.ncbi.nlm.nih.gov/pubmed/33479274
http://dx.doi.org/10.1038/s41598-021-80982-6
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author Russell, Jordan T.
Lauren Ruoss, J.
de la Cruz, Diomel
Li, Nan
Bazacliu, Catalina
Patton, Laura
McKinley, Kelley Lobean
Garrett, Timothy J.
Polin, Richard A.
Triplett, Eric W.
Neu, Josef
author_facet Russell, Jordan T.
Lauren Ruoss, J.
de la Cruz, Diomel
Li, Nan
Bazacliu, Catalina
Patton, Laura
McKinley, Kelley Lobean
Garrett, Timothy J.
Polin, Richard A.
Triplett, Eric W.
Neu, Josef
author_sort Russell, Jordan T.
collection PubMed
description Antibiotic use in neonates can have detrimental effects on the developing gut microbiome, increasing the risk of morbidity. A majority of preterm neonates receive antibiotics after birth without clear evidence to guide this practice. Here microbiome, metabolomic, and immune marker results from the routine early antibiotic use in symptomatic preterm Neonates (REASON) study are presented. The REASON study is the first trial to randomize symptomatic preterm neonates to receive or not receive antibiotics in the first 48 h after birth. Using 16S rRNA sequencing of stool samples collected longitudinally for 91 neonates, the effect of such antibiotic use on microbiome diversity is assessed. The results illustrate that type of nutrition shapes the early infant gut microbiome. By integrating data for the gut microbiome, stool metabolites, stool immune markers, and inferred metabolic pathways, an association was discovered between Veillonella and the neurotransmitter gamma-aminobutyric acid (GABA). These results suggest early antibiotic use may impact the gut-brain axis with the potential for consequences in early life development, a finding that needs to be validated in a larger cohort. Trial Registration This project is registered at clinicaltrials.gov under the name “Antibiotic ‘Dysbiosis’ in Preterm Infants” with trial number NCT02784821.
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spelling pubmed-78202852021-01-22 Antibiotics and the developing intestinal microbiome, metabolome and inflammatory environment in a randomized trial of preterm infants Russell, Jordan T. Lauren Ruoss, J. de la Cruz, Diomel Li, Nan Bazacliu, Catalina Patton, Laura McKinley, Kelley Lobean Garrett, Timothy J. Polin, Richard A. Triplett, Eric W. Neu, Josef Sci Rep Article Antibiotic use in neonates can have detrimental effects on the developing gut microbiome, increasing the risk of morbidity. A majority of preterm neonates receive antibiotics after birth without clear evidence to guide this practice. Here microbiome, metabolomic, and immune marker results from the routine early antibiotic use in symptomatic preterm Neonates (REASON) study are presented. The REASON study is the first trial to randomize symptomatic preterm neonates to receive or not receive antibiotics in the first 48 h after birth. Using 16S rRNA sequencing of stool samples collected longitudinally for 91 neonates, the effect of such antibiotic use on microbiome diversity is assessed. The results illustrate that type of nutrition shapes the early infant gut microbiome. By integrating data for the gut microbiome, stool metabolites, stool immune markers, and inferred metabolic pathways, an association was discovered between Veillonella and the neurotransmitter gamma-aminobutyric acid (GABA). These results suggest early antibiotic use may impact the gut-brain axis with the potential for consequences in early life development, a finding that needs to be validated in a larger cohort. Trial Registration This project is registered at clinicaltrials.gov under the name “Antibiotic ‘Dysbiosis’ in Preterm Infants” with trial number NCT02784821. Nature Publishing Group UK 2021-01-21 /pmc/articles/PMC7820285/ /pubmed/33479274 http://dx.doi.org/10.1038/s41598-021-80982-6 Text en © The Author(s) 2021 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
Russell, Jordan T.
Lauren Ruoss, J.
de la Cruz, Diomel
Li, Nan
Bazacliu, Catalina
Patton, Laura
McKinley, Kelley Lobean
Garrett, Timothy J.
Polin, Richard A.
Triplett, Eric W.
Neu, Josef
Antibiotics and the developing intestinal microbiome, metabolome and inflammatory environment in a randomized trial of preterm infants
title Antibiotics and the developing intestinal microbiome, metabolome and inflammatory environment in a randomized trial of preterm infants
title_full Antibiotics and the developing intestinal microbiome, metabolome and inflammatory environment in a randomized trial of preterm infants
title_fullStr Antibiotics and the developing intestinal microbiome, metabolome and inflammatory environment in a randomized trial of preterm infants
title_full_unstemmed Antibiotics and the developing intestinal microbiome, metabolome and inflammatory environment in a randomized trial of preterm infants
title_short Antibiotics and the developing intestinal microbiome, metabolome and inflammatory environment in a randomized trial of preterm infants
title_sort antibiotics and the developing intestinal microbiome, metabolome and inflammatory environment in a randomized trial of preterm infants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820285/
https://www.ncbi.nlm.nih.gov/pubmed/33479274
http://dx.doi.org/10.1038/s41598-021-80982-6
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