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High-throughput microbial culturomics using automation and machine learning
Pure bacterial cultures remain essential for detailed experimental and mechanistic studies in microbiome research, and traditional methods to isolate individual bacteria from complex microbial ecosystems are labor-intensive, difficult-to-scale and lack phenotype–genotype integration. Here we describ...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567565/ https://www.ncbi.nlm.nih.gov/pubmed/36805559 http://dx.doi.org/10.1038/s41587-023-01674-2 |
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author | Huang, Yiming Sheth, Ravi U. Zhao, Shijie Cohen, Lucas A. Dabaghi, Kendall Moody, Thomas Sun, Yiwei Ricaurte, Deirdre Richardson, Miles Velez-Cortes, Florencia Blazejewski, Tomasz Kaufman, Andrew Ronda, Carlotta Wang, Harris H. |
author_facet | Huang, Yiming Sheth, Ravi U. Zhao, Shijie Cohen, Lucas A. Dabaghi, Kendall Moody, Thomas Sun, Yiwei Ricaurte, Deirdre Richardson, Miles Velez-Cortes, Florencia Blazejewski, Tomasz Kaufman, Andrew Ronda, Carlotta Wang, Harris H. |
author_sort | Huang, Yiming |
collection | PubMed |
description | Pure bacterial cultures remain essential for detailed experimental and mechanistic studies in microbiome research, and traditional methods to isolate individual bacteria from complex microbial ecosystems are labor-intensive, difficult-to-scale and lack phenotype–genotype integration. Here we describe an open-source high-throughput robotic strain isolation platform for the rapid generation of isolates on demand. We develop a machine learning approach that leverages colony morphology and genomic data to maximize the diversity of microbes isolated and enable targeted picking of specific genera. Application of this platform on fecal samples from 20 humans yields personalized gut microbiome biobanks totaling 26,997 isolates that represented >80% of all abundant taxa. Spatial analysis on >100,000 visually captured colonies reveals cogrowth patterns between Ruminococcaceae, Bacteroidaceae, Coriobacteriaceae and Bifidobacteriaceae families that suggest important microbial interactions. Comparative analysis of 1,197 high-quality genomes from these biobanks shows interesting intra- and interpersonal strain evolution, selection and horizontal gene transfer. This culturomics framework should empower new research efforts to systematize the collection and quantitative analysis of imaging-based phenotypes with high-resolution genomics data for many emerging microbiome studies. |
format | Online Article Text |
id | pubmed-10567565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-105675652023-10-13 High-throughput microbial culturomics using automation and machine learning Huang, Yiming Sheth, Ravi U. Zhao, Shijie Cohen, Lucas A. Dabaghi, Kendall Moody, Thomas Sun, Yiwei Ricaurte, Deirdre Richardson, Miles Velez-Cortes, Florencia Blazejewski, Tomasz Kaufman, Andrew Ronda, Carlotta Wang, Harris H. Nat Biotechnol Article Pure bacterial cultures remain essential for detailed experimental and mechanistic studies in microbiome research, and traditional methods to isolate individual bacteria from complex microbial ecosystems are labor-intensive, difficult-to-scale and lack phenotype–genotype integration. Here we describe an open-source high-throughput robotic strain isolation platform for the rapid generation of isolates on demand. We develop a machine learning approach that leverages colony morphology and genomic data to maximize the diversity of microbes isolated and enable targeted picking of specific genera. Application of this platform on fecal samples from 20 humans yields personalized gut microbiome biobanks totaling 26,997 isolates that represented >80% of all abundant taxa. Spatial analysis on >100,000 visually captured colonies reveals cogrowth patterns between Ruminococcaceae, Bacteroidaceae, Coriobacteriaceae and Bifidobacteriaceae families that suggest important microbial interactions. Comparative analysis of 1,197 high-quality genomes from these biobanks shows interesting intra- and interpersonal strain evolution, selection and horizontal gene transfer. This culturomics framework should empower new research efforts to systematize the collection and quantitative analysis of imaging-based phenotypes with high-resolution genomics data for many emerging microbiome studies. Nature Publishing Group US 2023-02-20 2023 /pmc/articles/PMC10567565/ /pubmed/36805559 http://dx.doi.org/10.1038/s41587-023-01674-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Huang, Yiming Sheth, Ravi U. Zhao, Shijie Cohen, Lucas A. Dabaghi, Kendall Moody, Thomas Sun, Yiwei Ricaurte, Deirdre Richardson, Miles Velez-Cortes, Florencia Blazejewski, Tomasz Kaufman, Andrew Ronda, Carlotta Wang, Harris H. High-throughput microbial culturomics using automation and machine learning |
title | High-throughput microbial culturomics using automation and machine learning |
title_full | High-throughput microbial culturomics using automation and machine learning |
title_fullStr | High-throughput microbial culturomics using automation and machine learning |
title_full_unstemmed | High-throughput microbial culturomics using automation and machine learning |
title_short | High-throughput microbial culturomics using automation and machine learning |
title_sort | high-throughput microbial culturomics using automation and machine learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567565/ https://www.ncbi.nlm.nih.gov/pubmed/36805559 http://dx.doi.org/10.1038/s41587-023-01674-2 |
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