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Deconstructing the Soil Microbiome into Reduced-Complexity Functional Modules
The soil microbiome represents one of the most complex microbial communities on the planet, encompassing thousands of taxa and metabolic pathways, rendering holistic analyses computationally intensive and difficult. Here, we developed an alternative approach in which the complex soil microbiome was...
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/PMC7343995/ https://www.ncbi.nlm.nih.gov/pubmed/32636252 http://dx.doi.org/10.1128/mBio.01349-20 |
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author | Naylor, Dan Fansler, Sarah Brislawn, Colin Nelson, William C. Hofmockel, Kirsten S. Jansson, Janet K. McClure, Ryan |
author_facet | Naylor, Dan Fansler, Sarah Brislawn, Colin Nelson, William C. Hofmockel, Kirsten S. Jansson, Janet K. McClure, Ryan |
author_sort | Naylor, Dan |
collection | PubMed |
description | The soil microbiome represents one of the most complex microbial communities on the planet, encompassing thousands of taxa and metabolic pathways, rendering holistic analyses computationally intensive and difficult. Here, we developed an alternative approach in which the complex soil microbiome was broken into components (“functional modules”), based on metabolic capacities, for individual characterization. We hypothesized that reproducible, low-complexity communities that represent functional modules could be obtained through targeted enrichments and that, in combination, they would encompass a large extent of the soil microbiome diversity. Enrichments were performed on a starting soil inoculum with defined media based on specific carbon substrates, antibiotics, alternative electron acceptors under anaerobic conditions, or alternative growing conditions reflective of common field stresses. The resultant communities were evaluated through 16S rRNA amplicon sequencing. Less permissive modules (anaerobic conditions, complex polysaccharides, and certain stresses) resulted in more distinct community profiles with higher richness and more variability between replicates, whereas modules with simple substrates were dominated by fewer species and were more reproducible. Collectively, approximately 27% of unique taxa present in the liquid soil extract control were found across functional modules. Taxa that were underrepresented or undetected in the source soil were also enriched across the modules. Metatranscriptomic analyses were carried out on a subset of the modules to investigate differences in functional gene expression. These results demonstrate that by dissecting the soil microbiome into discrete components it is possible to obtain a more comprehensive view of the soil microbiome and its biochemical potential than would be possible using more holistic analyses. |
format | Online Article Text |
id | pubmed-7343995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73439952020-07-10 Deconstructing the Soil Microbiome into Reduced-Complexity Functional Modules Naylor, Dan Fansler, Sarah Brislawn, Colin Nelson, William C. Hofmockel, Kirsten S. Jansson, Janet K. McClure, Ryan mBio Research Article The soil microbiome represents one of the most complex microbial communities on the planet, encompassing thousands of taxa and metabolic pathways, rendering holistic analyses computationally intensive and difficult. Here, we developed an alternative approach in which the complex soil microbiome was broken into components (“functional modules”), based on metabolic capacities, for individual characterization. We hypothesized that reproducible, low-complexity communities that represent functional modules could be obtained through targeted enrichments and that, in combination, they would encompass a large extent of the soil microbiome diversity. Enrichments were performed on a starting soil inoculum with defined media based on specific carbon substrates, antibiotics, alternative electron acceptors under anaerobic conditions, or alternative growing conditions reflective of common field stresses. The resultant communities were evaluated through 16S rRNA amplicon sequencing. Less permissive modules (anaerobic conditions, complex polysaccharides, and certain stresses) resulted in more distinct community profiles with higher richness and more variability between replicates, whereas modules with simple substrates were dominated by fewer species and were more reproducible. Collectively, approximately 27% of unique taxa present in the liquid soil extract control were found across functional modules. Taxa that were underrepresented or undetected in the source soil were also enriched across the modules. Metatranscriptomic analyses were carried out on a subset of the modules to investigate differences in functional gene expression. These results demonstrate that by dissecting the soil microbiome into discrete components it is possible to obtain a more comprehensive view of the soil microbiome and its biochemical potential than would be possible using more holistic analyses. American Society for Microbiology 2020-07-07 /pmc/articles/PMC7343995/ /pubmed/32636252 http://dx.doi.org/10.1128/mBio.01349-20 Text en https://doi.org/10.1128/AuthorWarrantyLicense.v1 This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply. |
spellingShingle | Research Article Naylor, Dan Fansler, Sarah Brislawn, Colin Nelson, William C. Hofmockel, Kirsten S. Jansson, Janet K. McClure, Ryan Deconstructing the Soil Microbiome into Reduced-Complexity Functional Modules |
title | Deconstructing the Soil Microbiome into Reduced-Complexity Functional Modules |
title_full | Deconstructing the Soil Microbiome into Reduced-Complexity Functional Modules |
title_fullStr | Deconstructing the Soil Microbiome into Reduced-Complexity Functional Modules |
title_full_unstemmed | Deconstructing the Soil Microbiome into Reduced-Complexity Functional Modules |
title_short | Deconstructing the Soil Microbiome into Reduced-Complexity Functional Modules |
title_sort | deconstructing the soil microbiome into reduced-complexity functional modules |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343995/ https://www.ncbi.nlm.nih.gov/pubmed/32636252 http://dx.doi.org/10.1128/mBio.01349-20 |
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