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The Mini Colon Model: a benchtop multi-bioreactor system to investigate the gut microbiome
In vitro fermentation systems allow for the investigation of gut microbial communities with precise control of various physiological parameters while decoupling confounding factors from the human host. Current systems, such as the SHIME and Robogut, are large in footprint, lack multiplexing, and hav...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291644/ https://www.ncbi.nlm.nih.gov/pubmed/35844189 http://dx.doi.org/10.1080/19490976.2022.2096993 |
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author | Jin, Zijie Ng, Andy Maurice, Corinne F. Juncker, David |
author_facet | Jin, Zijie Ng, Andy Maurice, Corinne F. Juncker, David |
author_sort | Jin, Zijie |
collection | PubMed |
description | In vitro fermentation systems allow for the investigation of gut microbial communities with precise control of various physiological parameters while decoupling confounding factors from the human host. Current systems, such as the SHIME and Robogut, are large in footprint, lack multiplexing, and have low experimental throughput. Alternatives which address these shortcomings, such as the Mini Bioreactor Array system, are often reliant on expensive specialized equipment, which hinders wide replication across labs. Here, we present the Mini Colon Model (MiCoMo), a low-cost, benchtop multi-bioreactor system that simulates the human colon environment with physiologically relevant conditions. The device consists of triplicate bioreactors working independently of an anaerobic chamber and equipped with automated pH, temperature, and fluidic control. We conducted 14-d experiments and found that MiCoMo was able to support a stable complex microbiota community with a Shannon Index of 3.17 ± 0.65, from individual fecal samples after only 3–5 d of inoculation. MiCoMo also retained inter-sample microbial differences by developing closely related communities unique to each donor, while maintaining both minimal variations between replicate reactors (average Bray-Curtis similarity 0.72 ± 0.13) andday-to-day variations (average Bray-Curtis similarity 0.81±0.10) after this short stabilization period. Together, these results establish MiCoMo as an accessible system for studying gut microbial communities with high throughput and multiplexing capabilities. |
format | Online Article Text |
id | pubmed-9291644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-92916442022-07-19 The Mini Colon Model: a benchtop multi-bioreactor system to investigate the gut microbiome Jin, Zijie Ng, Andy Maurice, Corinne F. Juncker, David Gut Microbes Research Paper In vitro fermentation systems allow for the investigation of gut microbial communities with precise control of various physiological parameters while decoupling confounding factors from the human host. Current systems, such as the SHIME and Robogut, are large in footprint, lack multiplexing, and have low experimental throughput. Alternatives which address these shortcomings, such as the Mini Bioreactor Array system, are often reliant on expensive specialized equipment, which hinders wide replication across labs. Here, we present the Mini Colon Model (MiCoMo), a low-cost, benchtop multi-bioreactor system that simulates the human colon environment with physiologically relevant conditions. The device consists of triplicate bioreactors working independently of an anaerobic chamber and equipped with automated pH, temperature, and fluidic control. We conducted 14-d experiments and found that MiCoMo was able to support a stable complex microbiota community with a Shannon Index of 3.17 ± 0.65, from individual fecal samples after only 3–5 d of inoculation. MiCoMo also retained inter-sample microbial differences by developing closely related communities unique to each donor, while maintaining both minimal variations between replicate reactors (average Bray-Curtis similarity 0.72 ± 0.13) andday-to-day variations (average Bray-Curtis similarity 0.81±0.10) after this short stabilization period. Together, these results establish MiCoMo as an accessible system for studying gut microbial communities with high throughput and multiplexing capabilities. Taylor & Francis 2022-07-17 /pmc/articles/PMC9291644/ /pubmed/35844189 http://dx.doi.org/10.1080/19490976.2022.2096993 Text en © 2022 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 | Research Paper Jin, Zijie Ng, Andy Maurice, Corinne F. Juncker, David The Mini Colon Model: a benchtop multi-bioreactor system to investigate the gut microbiome |
title | The Mini Colon Model: a benchtop multi-bioreactor system to investigate the gut microbiome |
title_full | The Mini Colon Model: a benchtop multi-bioreactor system to investigate the gut microbiome |
title_fullStr | The Mini Colon Model: a benchtop multi-bioreactor system to investigate the gut microbiome |
title_full_unstemmed | The Mini Colon Model: a benchtop multi-bioreactor system to investigate the gut microbiome |
title_short | The Mini Colon Model: a benchtop multi-bioreactor system to investigate the gut microbiome |
title_sort | mini colon model: a benchtop multi-bioreactor system to investigate the gut microbiome |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291644/ https://www.ncbi.nlm.nih.gov/pubmed/35844189 http://dx.doi.org/10.1080/19490976.2022.2096993 |
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