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Deep learning predicts microbial interactions from self-organized spatiotemporal patterns
Microbial communities organize into spatial patterns that are largely governed by interspecies interactions. This phenomenon is an important metric for understanding community functional dynamics, yet the use of spatial patterns for predicting microbial interactions is currently lacking. Here we pro...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research Network of Computational and Structural Biotechnology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7298420/ https://www.ncbi.nlm.nih.gov/pubmed/32612750 http://dx.doi.org/10.1016/j.csbj.2020.05.023 |
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author | Lee, Joon-Yong Sadler, Natalie C. Egbert, Robert G. Anderton, Christopher R. Hofmockel, Kirsten S. Jansson, Janet K. Song, Hyun-Seob |
author_facet | Lee, Joon-Yong Sadler, Natalie C. Egbert, Robert G. Anderton, Christopher R. Hofmockel, Kirsten S. Jansson, Janet K. Song, Hyun-Seob |
author_sort | Lee, Joon-Yong |
collection | PubMed |
description | Microbial communities organize into spatial patterns that are largely governed by interspecies interactions. This phenomenon is an important metric for understanding community functional dynamics, yet the use of spatial patterns for predicting microbial interactions is currently lacking. Here we propose supervised deep learning as a new tool for network inference. An agent-based model was used to simulate the spatiotemporal evolution of two interacting organisms under diverse growth and interaction scenarios, the data of which was subsequently used to train deep neural networks. For small-size domains (100 µm × 100 µm) over which interaction coefficients are assumed to be invariant, we obtained fairly accurate predictions, as indicated by an average R(2) value of 0.84. In application to relatively larger domains (450 µm × 450 µm) where interaction coefficients are varying in space, deep learning models correctly predicted spatial distributions of interaction coefficients without any additional training. Lastly, we evaluated our model against real biological data obtained using Pseudomonas fluorescens and Escherichia coli co-cultures treated with polymeric chitin or N-acetylglucosamine, the hydrolysis product of chitin. While P. fluorescens can utilize both substrates for growth, E. coli lacked the ability to degrade chitin. Consistent with our expectations, our model predicted context-dependent interactions across two substrates, i.e., degrader-cheater relationship on chitin polymers and competition on monomers. The combined use of the agent-based model and machine learning algorithm successfully demonstrates how to infer microbial interactions from spatially distributed data, presenting itself as a useful tool for the analysis of more complex microbial community interactions. |
format | Online Article Text |
id | pubmed-7298420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-72984202020-06-30 Deep learning predicts microbial interactions from self-organized spatiotemporal patterns Lee, Joon-Yong Sadler, Natalie C. Egbert, Robert G. Anderton, Christopher R. Hofmockel, Kirsten S. Jansson, Janet K. Song, Hyun-Seob Comput Struct Biotechnol J Research Article Microbial communities organize into spatial patterns that are largely governed by interspecies interactions. This phenomenon is an important metric for understanding community functional dynamics, yet the use of spatial patterns for predicting microbial interactions is currently lacking. Here we propose supervised deep learning as a new tool for network inference. An agent-based model was used to simulate the spatiotemporal evolution of two interacting organisms under diverse growth and interaction scenarios, the data of which was subsequently used to train deep neural networks. For small-size domains (100 µm × 100 µm) over which interaction coefficients are assumed to be invariant, we obtained fairly accurate predictions, as indicated by an average R(2) value of 0.84. In application to relatively larger domains (450 µm × 450 µm) where interaction coefficients are varying in space, deep learning models correctly predicted spatial distributions of interaction coefficients without any additional training. Lastly, we evaluated our model against real biological data obtained using Pseudomonas fluorescens and Escherichia coli co-cultures treated with polymeric chitin or N-acetylglucosamine, the hydrolysis product of chitin. While P. fluorescens can utilize both substrates for growth, E. coli lacked the ability to degrade chitin. Consistent with our expectations, our model predicted context-dependent interactions across two substrates, i.e., degrader-cheater relationship on chitin polymers and competition on monomers. The combined use of the agent-based model and machine learning algorithm successfully demonstrates how to infer microbial interactions from spatially distributed data, presenting itself as a useful tool for the analysis of more complex microbial community interactions. Research Network of Computational and Structural Biotechnology 2020-05-29 /pmc/articles/PMC7298420/ /pubmed/32612750 http://dx.doi.org/10.1016/j.csbj.2020.05.023 Text en © 2020 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Lee, Joon-Yong Sadler, Natalie C. Egbert, Robert G. Anderton, Christopher R. Hofmockel, Kirsten S. Jansson, Janet K. Song, Hyun-Seob Deep learning predicts microbial interactions from self-organized spatiotemporal patterns |
title | Deep learning predicts microbial interactions from self-organized spatiotemporal patterns |
title_full | Deep learning predicts microbial interactions from self-organized spatiotemporal patterns |
title_fullStr | Deep learning predicts microbial interactions from self-organized spatiotemporal patterns |
title_full_unstemmed | Deep learning predicts microbial interactions from self-organized spatiotemporal patterns |
title_short | Deep learning predicts microbial interactions from self-organized spatiotemporal patterns |
title_sort | deep learning predicts microbial interactions from self-organized spatiotemporal patterns |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7298420/ https://www.ncbi.nlm.nih.gov/pubmed/32612750 http://dx.doi.org/10.1016/j.csbj.2020.05.023 |
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