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Enabling rational gut microbiome manipulations by understanding gut ecology through experimentally-evidenced in silico models
The gut microbiome has emerged as a contributing factor in non-communicable disease, rendering it a target of health-promoting interventions. Yet current understanding of the host-microbiome dynamic is insufficient to predict the variation in intervention outcomes across individuals. We explore the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432618/ https://www.ncbi.nlm.nih.gov/pubmed/34455914 http://dx.doi.org/10.1080/19490976.2021.1965698 |
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author | Molina Ortiz, Juan P. McClure, Dale D. Shanahan, Erin R. Dehghani, Fariba Holmes, Andrew J. Read, Mark N. |
author_facet | Molina Ortiz, Juan P. McClure, Dale D. Shanahan, Erin R. Dehghani, Fariba Holmes, Andrew J. Read, Mark N. |
author_sort | Molina Ortiz, Juan P. |
collection | PubMed |
description | The gut microbiome has emerged as a contributing factor in non-communicable disease, rendering it a target of health-promoting interventions. Yet current understanding of the host-microbiome dynamic is insufficient to predict the variation in intervention outcomes across individuals. We explore the mechanisms that underpin the gut bacterial ecosystem and highlight how a more complete understanding of this ecology will enable improved intervention outcomes. This ecology varies within the gut over space and time. Interventions disrupt these processes, with cascading consequences throughout the ecosystem. In vivo studies cannot isolate and probe these processes at the required spatiotemporal resolutions, and in vitro studies lack the representative complexity required. However, we highlight that, together, both approaches can inform in silico models that integrate cellular-level dynamics, can extrapolate to explain bacterial community outcomes, permit experimentation and observation over ecological processes at high spatiotemporal resolution, and can serve as predictive platforms on which to prototype interventions. Thus, it is a concerted integration of these techniques that will enable rational targeted manipulations of the gut ecosystem. |
format | Online Article Text |
id | pubmed-8432618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-84326182021-09-11 Enabling rational gut microbiome manipulations by understanding gut ecology through experimentally-evidenced in silico models Molina Ortiz, Juan P. McClure, Dale D. Shanahan, Erin R. Dehghani, Fariba Holmes, Andrew J. Read, Mark N. Gut Microbes Review The gut microbiome has emerged as a contributing factor in non-communicable disease, rendering it a target of health-promoting interventions. Yet current understanding of the host-microbiome dynamic is insufficient to predict the variation in intervention outcomes across individuals. We explore the mechanisms that underpin the gut bacterial ecosystem and highlight how a more complete understanding of this ecology will enable improved intervention outcomes. This ecology varies within the gut over space and time. Interventions disrupt these processes, with cascading consequences throughout the ecosystem. In vivo studies cannot isolate and probe these processes at the required spatiotemporal resolutions, and in vitro studies lack the representative complexity required. However, we highlight that, together, both approaches can inform in silico models that integrate cellular-level dynamics, can extrapolate to explain bacterial community outcomes, permit experimentation and observation over ecological processes at high spatiotemporal resolution, and can serve as predictive platforms on which to prototype interventions. Thus, it is a concerted integration of these techniques that will enable rational targeted manipulations of the gut ecosystem. Taylor & Francis 2021-08-30 /pmc/articles/PMC8432618/ /pubmed/34455914 http://dx.doi.org/10.1080/19490976.2021.1965698 Text en © 2021 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Molina Ortiz, Juan P. McClure, Dale D. Shanahan, Erin R. Dehghani, Fariba Holmes, Andrew J. Read, Mark N. Enabling rational gut microbiome manipulations by understanding gut ecology through experimentally-evidenced in silico models |
title | Enabling rational gut microbiome manipulations by understanding gut ecology through experimentally-evidenced in silico models |
title_full | Enabling rational gut microbiome manipulations by understanding gut ecology through experimentally-evidenced in silico models |
title_fullStr | Enabling rational gut microbiome manipulations by understanding gut ecology through experimentally-evidenced in silico models |
title_full_unstemmed | Enabling rational gut microbiome manipulations by understanding gut ecology through experimentally-evidenced in silico models |
title_short | Enabling rational gut microbiome manipulations by understanding gut ecology through experimentally-evidenced in silico models |
title_sort | enabling rational gut microbiome manipulations by understanding gut ecology through experimentally-evidenced in silico models |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432618/ https://www.ncbi.nlm.nih.gov/pubmed/34455914 http://dx.doi.org/10.1080/19490976.2021.1965698 |
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