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An in vitro platform for study of the human gut microbiome under an oxygen gradient
The complex, dynamic environment of the human lower gastrointestinal tract is colonized by hundreds of bacterial species that impact health and performance. Ex vivo study of the functional interactions between microbial community members in conditions representative of those in the gut is an ongoing...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073063/ https://www.ncbi.nlm.nih.gov/pubmed/37014472 http://dx.doi.org/10.1007/s10544-023-00653-3 |
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author | Comolli, James Walsh, David I. Bobrow, Johanna Lennartz, Chelsea L. Guido, Nicholas J. Thorsen, Todd |
author_facet | Comolli, James Walsh, David I. Bobrow, Johanna Lennartz, Chelsea L. Guido, Nicholas J. Thorsen, Todd |
author_sort | Comolli, James |
collection | PubMed |
description | The complex, dynamic environment of the human lower gastrointestinal tract is colonized by hundreds of bacterial species that impact health and performance. Ex vivo study of the functional interactions between microbial community members in conditions representative of those in the gut is an ongoing challenge. We have developed an in vitro 40-plex platform that provides an oxygen gradient to support simultaneous maintenance of microaerobic and anaerobic microbes from the gut microbiome that can aid in rapid characterization of microbial interactions and direct comparison of individual microbiome samples. In this report, we demonstrate that the platform more closely maintained the microbial diversity and composition of human donor fecal microbiome samples than strict anaerobic conditions. The oxygen gradient established in the platform allowed the stratification and subsequent sampling of diverse microbial subpopulations that colonize microaerobic and anaerobic micro-environments. With the ability to run forty samples in parallel, the platform has the potential to be used as a rapid screening tool to understand how the gut microbiome responds to environmental perturbations such as toxic compound exposure, dietary changes, or pharmaceutical treatments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10544-023-00653-3. |
format | Online Article Text |
id | pubmed-10073063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-100730632023-04-06 An in vitro platform for study of the human gut microbiome under an oxygen gradient Comolli, James Walsh, David I. Bobrow, Johanna Lennartz, Chelsea L. Guido, Nicholas J. Thorsen, Todd Biomed Microdevices Article The complex, dynamic environment of the human lower gastrointestinal tract is colonized by hundreds of bacterial species that impact health and performance. Ex vivo study of the functional interactions between microbial community members in conditions representative of those in the gut is an ongoing challenge. We have developed an in vitro 40-plex platform that provides an oxygen gradient to support simultaneous maintenance of microaerobic and anaerobic microbes from the gut microbiome that can aid in rapid characterization of microbial interactions and direct comparison of individual microbiome samples. In this report, we demonstrate that the platform more closely maintained the microbial diversity and composition of human donor fecal microbiome samples than strict anaerobic conditions. The oxygen gradient established in the platform allowed the stratification and subsequent sampling of diverse microbial subpopulations that colonize microaerobic and anaerobic micro-environments. With the ability to run forty samples in parallel, the platform has the potential to be used as a rapid screening tool to understand how the gut microbiome responds to environmental perturbations such as toxic compound exposure, dietary changes, or pharmaceutical treatments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10544-023-00653-3. Springer US 2023-04-04 2023 /pmc/articles/PMC10073063/ /pubmed/37014472 http://dx.doi.org/10.1007/s10544-023-00653-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Comolli, James Walsh, David I. Bobrow, Johanna Lennartz, Chelsea L. Guido, Nicholas J. Thorsen, Todd An in vitro platform for study of the human gut microbiome under an oxygen gradient |
title | An in vitro platform for study of the human gut microbiome under an oxygen gradient |
title_full | An in vitro platform for study of the human gut microbiome under an oxygen gradient |
title_fullStr | An in vitro platform for study of the human gut microbiome under an oxygen gradient |
title_full_unstemmed | An in vitro platform for study of the human gut microbiome under an oxygen gradient |
title_short | An in vitro platform for study of the human gut microbiome under an oxygen gradient |
title_sort | in vitro platform for study of the human gut microbiome under an oxygen gradient |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073063/ https://www.ncbi.nlm.nih.gov/pubmed/37014472 http://dx.doi.org/10.1007/s10544-023-00653-3 |
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