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Preterm gut microbiota and metabolome following discharge from intensive care
The development of the preterm gut microbiome is important for immediate and longer-term health following birth. We aimed to determine if modifications to the preterm gut on the neonatal intensive care unit (NICU) impacted the gut microbiota and metabolome long-term. Stool samples were collected fro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657104/ https://www.ncbi.nlm.nih.gov/pubmed/26598071 http://dx.doi.org/10.1038/srep17141 |
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author | Stewart, Christopher J. Skeath, Tom Nelson, Andrew Fernstad, Sara J. Marrs, Emma C. L. Perry, John D. Cummings, Stephen P. Berrington, Janet E. Embleton, Nicholas D. |
author_facet | Stewart, Christopher J. Skeath, Tom Nelson, Andrew Fernstad, Sara J. Marrs, Emma C. L. Perry, John D. Cummings, Stephen P. Berrington, Janet E. Embleton, Nicholas D. |
author_sort | Stewart, Christopher J. |
collection | PubMed |
description | The development of the preterm gut microbiome is important for immediate and longer-term health following birth. We aimed to determine if modifications to the preterm gut on the neonatal intensive care unit (NICU) impacted the gut microbiota and metabolome long-term. Stool samples were collected from 29 infants ages 1–3 years post discharge (PD) from a single NICU. Additional NICU samples were included from 14/29 infants. Being diagnosed with disease or receiving increased antibiotics while on the NICU did not significantly impact the microbiome PD. Significant decreases in common NICU organisms including K. oxytoca and E. faecalis and increases in common adult organisms including Akkermansia sp., Blautia sp., and Bacteroides sp. and significantly different Shannon diversity was shown between NICU and PD samples. The metabolome increased in complexity, but while PD samples had unique bacterial profiles we observed comparable metabolomic profiles. The preterm gut microbiome is able to develop complexity comparable to healthy term infants despite limited environmental exposures, high levels of antibiotic administration, and of the presence of serious disease. Further work is needed to establish the direct effect of weaning as a key event in promoting future gut health. |
format | Online Article Text |
id | pubmed-4657104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46571042015-11-30 Preterm gut microbiota and metabolome following discharge from intensive care Stewart, Christopher J. Skeath, Tom Nelson, Andrew Fernstad, Sara J. Marrs, Emma C. L. Perry, John D. Cummings, Stephen P. Berrington, Janet E. Embleton, Nicholas D. Sci Rep Article The development of the preterm gut microbiome is important for immediate and longer-term health following birth. We aimed to determine if modifications to the preterm gut on the neonatal intensive care unit (NICU) impacted the gut microbiota and metabolome long-term. Stool samples were collected from 29 infants ages 1–3 years post discharge (PD) from a single NICU. Additional NICU samples were included from 14/29 infants. Being diagnosed with disease or receiving increased antibiotics while on the NICU did not significantly impact the microbiome PD. Significant decreases in common NICU organisms including K. oxytoca and E. faecalis and increases in common adult organisms including Akkermansia sp., Blautia sp., and Bacteroides sp. and significantly different Shannon diversity was shown between NICU and PD samples. The metabolome increased in complexity, but while PD samples had unique bacterial profiles we observed comparable metabolomic profiles. The preterm gut microbiome is able to develop complexity comparable to healthy term infants despite limited environmental exposures, high levels of antibiotic administration, and of the presence of serious disease. Further work is needed to establish the direct effect of weaning as a key event in promoting future gut health. Nature Publishing Group 2015-11-24 /pmc/articles/PMC4657104/ /pubmed/26598071 http://dx.doi.org/10.1038/srep17141 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Stewart, Christopher J. Skeath, Tom Nelson, Andrew Fernstad, Sara J. Marrs, Emma C. L. Perry, John D. Cummings, Stephen P. Berrington, Janet E. Embleton, Nicholas D. Preterm gut microbiota and metabolome following discharge from intensive care |
title | Preterm gut microbiota and metabolome following discharge from intensive care |
title_full | Preterm gut microbiota and metabolome following discharge from intensive care |
title_fullStr | Preterm gut microbiota and metabolome following discharge from intensive care |
title_full_unstemmed | Preterm gut microbiota and metabolome following discharge from intensive care |
title_short | Preterm gut microbiota and metabolome following discharge from intensive care |
title_sort | preterm gut microbiota and metabolome following discharge from intensive care |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657104/ https://www.ncbi.nlm.nih.gov/pubmed/26598071 http://dx.doi.org/10.1038/srep17141 |
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