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Investigating the dynamics of microbial consortia in spatially structured environments

The spatial organization of microbial communities arises from a complex interplay of biotic and abiotic interactions, and is a major determinant of ecosystem functions. Here we design a microfluidic platform to investigate how the spatial arrangement of microbes impacts gene expression and growth. W...

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Autores principales: Gupta, Sonali, Ross, Tyler D., Gomez, Marcella M., Grant, Job L., Romero, Philip A., Venturelli, Ophelia S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7228966/
https://www.ncbi.nlm.nih.gov/pubmed/32415107
http://dx.doi.org/10.1038/s41467-020-16200-0
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author Gupta, Sonali
Ross, Tyler D.
Gomez, Marcella M.
Grant, Job L.
Romero, Philip A.
Venturelli, Ophelia S.
author_facet Gupta, Sonali
Ross, Tyler D.
Gomez, Marcella M.
Grant, Job L.
Romero, Philip A.
Venturelli, Ophelia S.
author_sort Gupta, Sonali
collection PubMed
description The spatial organization of microbial communities arises from a complex interplay of biotic and abiotic interactions, and is a major determinant of ecosystem functions. Here we design a microfluidic platform to investigate how the spatial arrangement of microbes impacts gene expression and growth. We elucidate key biochemical parameters that dictate the mapping between spatial positioning and gene expression patterns. We show that distance can establish a low-pass filter to periodic inputs and can enhance the fidelity of information processing. Positive and negative feedback can play disparate roles in the synchronization and robustness of a genetic oscillator distributed between two strains to spatial separation. Quantification of growth and metabolite release in an amino-acid auxotroph community demonstrates that the interaction network and stability of the community are highly sensitive to temporal perturbations and spatial arrangements. In sum, our microfluidic platform can quantify spatiotemporal parameters influencing diffusion-mediated interactions in microbial consortia.
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spelling pubmed-72289662020-06-05 Investigating the dynamics of microbial consortia in spatially structured environments Gupta, Sonali Ross, Tyler D. Gomez, Marcella M. Grant, Job L. Romero, Philip A. Venturelli, Ophelia S. Nat Commun Article The spatial organization of microbial communities arises from a complex interplay of biotic and abiotic interactions, and is a major determinant of ecosystem functions. Here we design a microfluidic platform to investigate how the spatial arrangement of microbes impacts gene expression and growth. We elucidate key biochemical parameters that dictate the mapping between spatial positioning and gene expression patterns. We show that distance can establish a low-pass filter to periodic inputs and can enhance the fidelity of information processing. Positive and negative feedback can play disparate roles in the synchronization and robustness of a genetic oscillator distributed between two strains to spatial separation. Quantification of growth and metabolite release in an amino-acid auxotroph community demonstrates that the interaction network and stability of the community are highly sensitive to temporal perturbations and spatial arrangements. In sum, our microfluidic platform can quantify spatiotemporal parameters influencing diffusion-mediated interactions in microbial consortia. Nature Publishing Group UK 2020-05-15 /pmc/articles/PMC7228966/ /pubmed/32415107 http://dx.doi.org/10.1038/s41467-020-16200-0 Text en © The Author(s) 2020 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/.
spellingShingle Article
Gupta, Sonali
Ross, Tyler D.
Gomez, Marcella M.
Grant, Job L.
Romero, Philip A.
Venturelli, Ophelia S.
Investigating the dynamics of microbial consortia in spatially structured environments
title Investigating the dynamics of microbial consortia in spatially structured environments
title_full Investigating the dynamics of microbial consortia in spatially structured environments
title_fullStr Investigating the dynamics of microbial consortia in spatially structured environments
title_full_unstemmed Investigating the dynamics of microbial consortia in spatially structured environments
title_short Investigating the dynamics of microbial consortia in spatially structured environments
title_sort investigating the dynamics of microbial consortia in spatially structured environments
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7228966/
https://www.ncbi.nlm.nih.gov/pubmed/32415107
http://dx.doi.org/10.1038/s41467-020-16200-0
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