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Stability and resilience of the intestinal microbiota in children in daycare – a 12 month cohort study
BACKGROUND: We performed a 12-month cohort study of the stability and resilience of the intestinal microbiota of healthy children in daycare in Denmark in relation to diarrheal events and exposure to known risk factors for gastrointestinal health such as travelling and antibiotic use. In addition, w...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303881/ https://www.ncbi.nlm.nih.gov/pubmed/30579350 http://dx.doi.org/10.1186/s12866-018-1367-5 |
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author | Mortensen, Martin Steen Hebbelstrup Jensen, Betina Williams, Jeanne Brejnrod, Asker Daniel O’Brien Andersen, Lee Röser, Dennis Andreassen, Bente Utoft Petersen, Andreas Munk Stensvold, Christen Rune Sørensen, Søren Johannes Krogfelt, Karen Angeliki |
author_facet | Mortensen, Martin Steen Hebbelstrup Jensen, Betina Williams, Jeanne Brejnrod, Asker Daniel O’Brien Andersen, Lee Röser, Dennis Andreassen, Bente Utoft Petersen, Andreas Munk Stensvold, Christen Rune Sørensen, Søren Johannes Krogfelt, Karen Angeliki |
author_sort | Mortensen, Martin Steen |
collection | PubMed |
description | BACKGROUND: We performed a 12-month cohort study of the stability and resilience of the intestinal microbiota of healthy children in daycare in Denmark in relation to diarrheal events and exposure to known risk factors for gastrointestinal health such as travelling and antibiotic use. In addition, we analyzed how gut microbiota recover from such exposures. RESULTS: We monitored 32 children in daycare aged 1–6 years. Fecal samples were submitted every second month during a one-year observational period. Information regarding exposures and diarrheal episodes was obtained through questionnaires. Bacterial communities were identified using 16S rRNA gene sequencing. The core microbiota (mean abundance > 95%) dominated the intestinal microbiota, and none of the tested exposures (diarrheal events, travel, antibiotic use) were associated with decreases in the relative abundance of the core microbiota. Samples exhibited lower intra-individual variation than inter-individual variation. Half of all the variation between samples was explained by which child a sample originated from. Age explained 7.6–9.6% of the variation, while traveling, diarrheal events, and antibiotic use explained minor parts of the beta diversity. We found an age-dependent increase of alpha diversity in children aged 1–3 years, and while diarrheal events caused a decrease in alpha diversity, a recovery time of 40–45 days was observed. Among children having had a diarrheal event, we observed a 10x higher relative abundance of Prevotella. After travelling, a higher abundance of two Bacteroides species and 40% less Lachnospiraceae were seen. Antibiotic use did not correlate with changes in the abundance of any bacteria. CONCLUSION: We present data showing that Danish children in daycare have stable intestinal microbiota, resilient to the exposures investigated. An early age-dependent increase in the diversity was demonstrated. Diarrheal episodes decreased alpha diversity with an estimated recovery time of 40–45 days. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1367-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6303881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63038812018-12-31 Stability and resilience of the intestinal microbiota in children in daycare – a 12 month cohort study Mortensen, Martin Steen Hebbelstrup Jensen, Betina Williams, Jeanne Brejnrod, Asker Daniel O’Brien Andersen, Lee Röser, Dennis Andreassen, Bente Utoft Petersen, Andreas Munk Stensvold, Christen Rune Sørensen, Søren Johannes Krogfelt, Karen Angeliki BMC Microbiol Research Article BACKGROUND: We performed a 12-month cohort study of the stability and resilience of the intestinal microbiota of healthy children in daycare in Denmark in relation to diarrheal events and exposure to known risk factors for gastrointestinal health such as travelling and antibiotic use. In addition, we analyzed how gut microbiota recover from such exposures. RESULTS: We monitored 32 children in daycare aged 1–6 years. Fecal samples were submitted every second month during a one-year observational period. Information regarding exposures and diarrheal episodes was obtained through questionnaires. Bacterial communities were identified using 16S rRNA gene sequencing. The core microbiota (mean abundance > 95%) dominated the intestinal microbiota, and none of the tested exposures (diarrheal events, travel, antibiotic use) were associated with decreases in the relative abundance of the core microbiota. Samples exhibited lower intra-individual variation than inter-individual variation. Half of all the variation between samples was explained by which child a sample originated from. Age explained 7.6–9.6% of the variation, while traveling, diarrheal events, and antibiotic use explained minor parts of the beta diversity. We found an age-dependent increase of alpha diversity in children aged 1–3 years, and while diarrheal events caused a decrease in alpha diversity, a recovery time of 40–45 days was observed. Among children having had a diarrheal event, we observed a 10x higher relative abundance of Prevotella. After travelling, a higher abundance of two Bacteroides species and 40% less Lachnospiraceae were seen. Antibiotic use did not correlate with changes in the abundance of any bacteria. CONCLUSION: We present data showing that Danish children in daycare have stable intestinal microbiota, resilient to the exposures investigated. An early age-dependent increase in the diversity was demonstrated. Diarrheal episodes decreased alpha diversity with an estimated recovery time of 40–45 days. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1367-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-22 /pmc/articles/PMC6303881/ /pubmed/30579350 http://dx.doi.org/10.1186/s12866-018-1367-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Mortensen, Martin Steen Hebbelstrup Jensen, Betina Williams, Jeanne Brejnrod, Asker Daniel O’Brien Andersen, Lee Röser, Dennis Andreassen, Bente Utoft Petersen, Andreas Munk Stensvold, Christen Rune Sørensen, Søren Johannes Krogfelt, Karen Angeliki Stability and resilience of the intestinal microbiota in children in daycare – a 12 month cohort study |
title | Stability and resilience of the intestinal microbiota in children in daycare – a 12 month cohort study |
title_full | Stability and resilience of the intestinal microbiota in children in daycare – a 12 month cohort study |
title_fullStr | Stability and resilience of the intestinal microbiota in children in daycare – a 12 month cohort study |
title_full_unstemmed | Stability and resilience of the intestinal microbiota in children in daycare – a 12 month cohort study |
title_short | Stability and resilience of the intestinal microbiota in children in daycare – a 12 month cohort study |
title_sort | stability and resilience of the intestinal microbiota in children in daycare – a 12 month cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303881/ https://www.ncbi.nlm.nih.gov/pubmed/30579350 http://dx.doi.org/10.1186/s12866-018-1367-5 |
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