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Growth phase estimation for abundant bacterial populations sampled longitudinally from human stool metagenomes
Longitudinal sampling of the stool has yielded important insights into the ecological dynamics of the human gut microbiome. However, human stool samples are available approximately once per day, while commensal population doubling times are likely on the order of minutes-to-hours. Despite this misma...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502120/ https://www.ncbi.nlm.nih.gov/pubmed/37709733 http://dx.doi.org/10.1038/s41467-023-41424-1 |
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author | Lim, Joe J. Diener, Christian Wilson, James Valenzuela, Jacob J. Baliga, Nitin S. Gibbons, Sean M. |
author_facet | Lim, Joe J. Diener, Christian Wilson, James Valenzuela, Jacob J. Baliga, Nitin S. Gibbons, Sean M. |
author_sort | Lim, Joe J. |
collection | PubMed |
description | Longitudinal sampling of the stool has yielded important insights into the ecological dynamics of the human gut microbiome. However, human stool samples are available approximately once per day, while commensal population doubling times are likely on the order of minutes-to-hours. Despite this mismatch in timescales, much of the prior work on human gut microbiome time series modeling has assumed that day-to-day fluctuations in taxon abundances are related to population growth or death rates, which is likely not the case. Here, we propose an alternative model of the human gut as a stationary system, where population dynamics occur internally and the bacterial population sizes measured in a bolus of stool represent a steady-state endpoint of these dynamics. We formalize this idea as stochastic logistic growth. We show how this model provides a path toward estimating the growth phases of gut bacterial populations in situ. We validate our model predictions using an in vitro Escherichia coli growth experiment. Finally, we show how this method can be applied to densely-sampled human stool metagenomic time series data. We discuss how these growth phase estimates may be used to better inform metabolic modeling in flow-through ecosystems, like animal guts or industrial bioreactors. |
format | Online Article Text |
id | pubmed-10502120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105021202023-09-16 Growth phase estimation for abundant bacterial populations sampled longitudinally from human stool metagenomes Lim, Joe J. Diener, Christian Wilson, James Valenzuela, Jacob J. Baliga, Nitin S. Gibbons, Sean M. Nat Commun Article Longitudinal sampling of the stool has yielded important insights into the ecological dynamics of the human gut microbiome. However, human stool samples are available approximately once per day, while commensal population doubling times are likely on the order of minutes-to-hours. Despite this mismatch in timescales, much of the prior work on human gut microbiome time series modeling has assumed that day-to-day fluctuations in taxon abundances are related to population growth or death rates, which is likely not the case. Here, we propose an alternative model of the human gut as a stationary system, where population dynamics occur internally and the bacterial population sizes measured in a bolus of stool represent a steady-state endpoint of these dynamics. We formalize this idea as stochastic logistic growth. We show how this model provides a path toward estimating the growth phases of gut bacterial populations in situ. We validate our model predictions using an in vitro Escherichia coli growth experiment. Finally, we show how this method can be applied to densely-sampled human stool metagenomic time series data. We discuss how these growth phase estimates may be used to better inform metabolic modeling in flow-through ecosystems, like animal guts or industrial bioreactors. Nature Publishing Group UK 2023-09-14 /pmc/articles/PMC10502120/ /pubmed/37709733 http://dx.doi.org/10.1038/s41467-023-41424-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lim, Joe J. Diener, Christian Wilson, James Valenzuela, Jacob J. Baliga, Nitin S. Gibbons, Sean M. Growth phase estimation for abundant bacterial populations sampled longitudinally from human stool metagenomes |
title | Growth phase estimation for abundant bacterial populations sampled longitudinally from human stool metagenomes |
title_full | Growth phase estimation for abundant bacterial populations sampled longitudinally from human stool metagenomes |
title_fullStr | Growth phase estimation for abundant bacterial populations sampled longitudinally from human stool metagenomes |
title_full_unstemmed | Growth phase estimation for abundant bacterial populations sampled longitudinally from human stool metagenomes |
title_short | Growth phase estimation for abundant bacterial populations sampled longitudinally from human stool metagenomes |
title_sort | growth phase estimation for abundant bacterial populations sampled longitudinally from human stool metagenomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502120/ https://www.ncbi.nlm.nih.gov/pubmed/37709733 http://dx.doi.org/10.1038/s41467-023-41424-1 |
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