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Habitat geometry in artificial microstructure affects bacterial and fungal growth, interactions, and substrate degradation

Microhabitat conditions determine the magnitude and speed of microbial processes but have been challenging to investigate. In this study we used microfluidic devices to determine the effect of the spatial distortion of a pore space on fungal and bacterial growth, interactions, and substrate degradat...

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Autores principales: Arellano-Caicedo, Carlos, Ohlsson, Pelle, Bengtsson, Martin, Beech, Jason P., Hammer, Edith C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548513/
https://www.ncbi.nlm.nih.gov/pubmed/34702996
http://dx.doi.org/10.1038/s42003-021-02736-4
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author Arellano-Caicedo, Carlos
Ohlsson, Pelle
Bengtsson, Martin
Beech, Jason P.
Hammer, Edith C.
author_facet Arellano-Caicedo, Carlos
Ohlsson, Pelle
Bengtsson, Martin
Beech, Jason P.
Hammer, Edith C.
author_sort Arellano-Caicedo, Carlos
collection PubMed
description Microhabitat conditions determine the magnitude and speed of microbial processes but have been challenging to investigate. In this study we used microfluidic devices to determine the effect of the spatial distortion of a pore space on fungal and bacterial growth, interactions, and substrate degradation. The devices contained channels differing in bending angles and order. Sharper angles reduced fungal and bacterial biomass, especially when angles were repeated in the same direction. Substrate degradation was only decreased by sharper angles when fungi and bacteria were grown together. Investigation at the cellular scale suggests that this was caused by fungal habitat modification, since hyphae branched in sharp and repeated turns, blocking the dispersal of bacteria and the substrate. Our results demonstrate how the geometry of microstructures can influence microbial activity. This can be transferable to soil pore spaces, where spatial occlusion and microbial feedback on microstructures is thought to explain organic matter stabilization.
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spelling pubmed-85485132021-10-29 Habitat geometry in artificial microstructure affects bacterial and fungal growth, interactions, and substrate degradation Arellano-Caicedo, Carlos Ohlsson, Pelle Bengtsson, Martin Beech, Jason P. Hammer, Edith C. Commun Biol Article Microhabitat conditions determine the magnitude and speed of microbial processes but have been challenging to investigate. In this study we used microfluidic devices to determine the effect of the spatial distortion of a pore space on fungal and bacterial growth, interactions, and substrate degradation. The devices contained channels differing in bending angles and order. Sharper angles reduced fungal and bacterial biomass, especially when angles were repeated in the same direction. Substrate degradation was only decreased by sharper angles when fungi and bacteria were grown together. Investigation at the cellular scale suggests that this was caused by fungal habitat modification, since hyphae branched in sharp and repeated turns, blocking the dispersal of bacteria and the substrate. Our results demonstrate how the geometry of microstructures can influence microbial activity. This can be transferable to soil pore spaces, where spatial occlusion and microbial feedback on microstructures is thought to explain organic matter stabilization. Nature Publishing Group UK 2021-10-26 /pmc/articles/PMC8548513/ /pubmed/34702996 http://dx.doi.org/10.1038/s42003-021-02736-4 Text en © The Author(s) 2021 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
Arellano-Caicedo, Carlos
Ohlsson, Pelle
Bengtsson, Martin
Beech, Jason P.
Hammer, Edith C.
Habitat geometry in artificial microstructure affects bacterial and fungal growth, interactions, and substrate degradation
title Habitat geometry in artificial microstructure affects bacterial and fungal growth, interactions, and substrate degradation
title_full Habitat geometry in artificial microstructure affects bacterial and fungal growth, interactions, and substrate degradation
title_fullStr Habitat geometry in artificial microstructure affects bacterial and fungal growth, interactions, and substrate degradation
title_full_unstemmed Habitat geometry in artificial microstructure affects bacterial and fungal growth, interactions, and substrate degradation
title_short Habitat geometry in artificial microstructure affects bacterial and fungal growth, interactions, and substrate degradation
title_sort habitat geometry in artificial microstructure affects bacterial and fungal growth, interactions, and substrate degradation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548513/
https://www.ncbi.nlm.nih.gov/pubmed/34702996
http://dx.doi.org/10.1038/s42003-021-02736-4
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