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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...

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Autores principales: Lee, Joon-Yong, Sadler, Natalie C., Egbert, Robert G., Anderton, Christopher R., Hofmockel, Kirsten S., Jansson, Janet K., Song, Hyun-Seob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2020
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.
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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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