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Higher-Order Interactions Dampen Pairwise Competition in the Zebrafish Gut Microbiome
The microbial communities resident in animal intestines are composed of multiple species that together play important roles in host development, health, and disease. Due to the complexity of these communities and the difficulty of characterizing them in situ, the determinants of microbial compositio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554667/ https://www.ncbi.nlm.nih.gov/pubmed/33051365 http://dx.doi.org/10.1128/mBio.01667-20 |
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author | Sundarraman, Deepika Hay, Edouard A. Martins, Dylan M. Shields, Drew S. Pettinari, Noah L. Parthasarathy, Raghuveer |
author_facet | Sundarraman, Deepika Hay, Edouard A. Martins, Dylan M. Shields, Drew S. Pettinari, Noah L. Parthasarathy, Raghuveer |
author_sort | Sundarraman, Deepika |
collection | PubMed |
description | The microbial communities resident in animal intestines are composed of multiple species that together play important roles in host development, health, and disease. Due to the complexity of these communities and the difficulty of characterizing them in situ, the determinants of microbial composition remain largely unknown. Further, it is unclear for many multispecies consortia whether their species-level makeup can be predicted based on an understanding of pairwise species interactions or whether higher-order interactions are needed to explain emergent compositions. To address this, we examine commensal intestinal microbes in larval zebrafish, initially raised germfree, to allow the introduction of controlled combinations of bacterial species. Using a dissection and plating assay, we demonstrate the construction of communities of one to five bacterial species and show that the outcomes from the two-species competitions fail to predict species abundances in more complex communities. With multiple species present, interbacterial interactions become weaker, suggesting that higher-order interactions in the vertebrate gut stabilize complex communities. |
format | Online Article Text |
id | pubmed-7554667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-75546672020-10-19 Higher-Order Interactions Dampen Pairwise Competition in the Zebrafish Gut Microbiome Sundarraman, Deepika Hay, Edouard A. Martins, Dylan M. Shields, Drew S. Pettinari, Noah L. Parthasarathy, Raghuveer mBio Research Article The microbial communities resident in animal intestines are composed of multiple species that together play important roles in host development, health, and disease. Due to the complexity of these communities and the difficulty of characterizing them in situ, the determinants of microbial composition remain largely unknown. Further, it is unclear for many multispecies consortia whether their species-level makeup can be predicted based on an understanding of pairwise species interactions or whether higher-order interactions are needed to explain emergent compositions. To address this, we examine commensal intestinal microbes in larval zebrafish, initially raised germfree, to allow the introduction of controlled combinations of bacterial species. Using a dissection and plating assay, we demonstrate the construction of communities of one to five bacterial species and show that the outcomes from the two-species competitions fail to predict species abundances in more complex communities. With multiple species present, interbacterial interactions become weaker, suggesting that higher-order interactions in the vertebrate gut stabilize complex communities. American Society for Microbiology 2020-10-13 /pmc/articles/PMC7554667/ /pubmed/33051365 http://dx.doi.org/10.1128/mBio.01667-20 Text en Copyright © 2020 Sundarraman et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Sundarraman, Deepika Hay, Edouard A. Martins, Dylan M. Shields, Drew S. Pettinari, Noah L. Parthasarathy, Raghuveer Higher-Order Interactions Dampen Pairwise Competition in the Zebrafish Gut Microbiome |
title | Higher-Order Interactions Dampen Pairwise Competition in the Zebrafish Gut Microbiome |
title_full | Higher-Order Interactions Dampen Pairwise Competition in the Zebrafish Gut Microbiome |
title_fullStr | Higher-Order Interactions Dampen Pairwise Competition in the Zebrafish Gut Microbiome |
title_full_unstemmed | Higher-Order Interactions Dampen Pairwise Competition in the Zebrafish Gut Microbiome |
title_short | Higher-Order Interactions Dampen Pairwise Competition in the Zebrafish Gut Microbiome |
title_sort | higher-order interactions dampen pairwise competition in the zebrafish gut microbiome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554667/ https://www.ncbi.nlm.nih.gov/pubmed/33051365 http://dx.doi.org/10.1128/mBio.01667-20 |
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