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Facilitative interaction networks in experimental microbial community dynamics

Facilitative interactions between microbial species are ubiquitous in various types of ecosystems on the Earth. Therefore, inferring how entangled webs of interspecific interactions shift through time in microbial ecosystems is an essential step for understanding ecological processes driving microbi...

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Autores principales: Fujita, Hiroaki, Ushio, Masayuki, Suzuki, Kenta, Abe, Masato S., Yamamichi, Masato, Okazaki, Yusuke, Canarini, Alberto, Hayashi, Ibuki, Fukushima, Keitaro, Fukuda, Shinji, Kiers, E. Toby, Toju, Hirokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126487/
https://www.ncbi.nlm.nih.gov/pubmed/37113242
http://dx.doi.org/10.3389/fmicb.2023.1153952
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author Fujita, Hiroaki
Ushio, Masayuki
Suzuki, Kenta
Abe, Masato S.
Yamamichi, Masato
Okazaki, Yusuke
Canarini, Alberto
Hayashi, Ibuki
Fukushima, Keitaro
Fukuda, Shinji
Kiers, E. Toby
Toju, Hirokazu
author_facet Fujita, Hiroaki
Ushio, Masayuki
Suzuki, Kenta
Abe, Masato S.
Yamamichi, Masato
Okazaki, Yusuke
Canarini, Alberto
Hayashi, Ibuki
Fukushima, Keitaro
Fukuda, Shinji
Kiers, E. Toby
Toju, Hirokazu
author_sort Fujita, Hiroaki
collection PubMed
description Facilitative interactions between microbial species are ubiquitous in various types of ecosystems on the Earth. Therefore, inferring how entangled webs of interspecific interactions shift through time in microbial ecosystems is an essential step for understanding ecological processes driving microbiome dynamics. By compiling shotgun metagenomic sequencing data of an experimental microbial community, we examined how the architectural features of facilitative interaction networks could change through time. A metabolic modeling approach for estimating dependence between microbial genomes (species) allowed us to infer the network structure of potential facilitative interactions at 13 time points through the 110-day monitoring of experimental microbiomes. We then found that positive feedback loops, which were theoretically predicted to promote cascade breakdown of ecological communities, existed within the inferred networks of metabolic interactions prior to the drastic community-compositional shift observed in the microbiome time-series. We further applied “directed-graph” analyses to pinpoint potential keystone species located at the “upper stream” positions of such feedback loops. These analyses on facilitative interactions will help us understand key mechanisms causing catastrophic shifts in microbial community structure.
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spelling pubmed-101264872023-04-26 Facilitative interaction networks in experimental microbial community dynamics Fujita, Hiroaki Ushio, Masayuki Suzuki, Kenta Abe, Masato S. Yamamichi, Masato Okazaki, Yusuke Canarini, Alberto Hayashi, Ibuki Fukushima, Keitaro Fukuda, Shinji Kiers, E. Toby Toju, Hirokazu Front Microbiol Microbiology Facilitative interactions between microbial species are ubiquitous in various types of ecosystems on the Earth. Therefore, inferring how entangled webs of interspecific interactions shift through time in microbial ecosystems is an essential step for understanding ecological processes driving microbiome dynamics. By compiling shotgun metagenomic sequencing data of an experimental microbial community, we examined how the architectural features of facilitative interaction networks could change through time. A metabolic modeling approach for estimating dependence between microbial genomes (species) allowed us to infer the network structure of potential facilitative interactions at 13 time points through the 110-day monitoring of experimental microbiomes. We then found that positive feedback loops, which were theoretically predicted to promote cascade breakdown of ecological communities, existed within the inferred networks of metabolic interactions prior to the drastic community-compositional shift observed in the microbiome time-series. We further applied “directed-graph” analyses to pinpoint potential keystone species located at the “upper stream” positions of such feedback loops. These analyses on facilitative interactions will help us understand key mechanisms causing catastrophic shifts in microbial community structure. Frontiers Media S.A. 2023-04-11 /pmc/articles/PMC10126487/ /pubmed/37113242 http://dx.doi.org/10.3389/fmicb.2023.1153952 Text en Copyright © 2023 Fujita, Ushio, Suzuki, Abe, Yamamichi, Okazaki, Canarini, Hayashi, Fukushima, Fukuda, Kiers and Toju. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Fujita, Hiroaki
Ushio, Masayuki
Suzuki, Kenta
Abe, Masato S.
Yamamichi, Masato
Okazaki, Yusuke
Canarini, Alberto
Hayashi, Ibuki
Fukushima, Keitaro
Fukuda, Shinji
Kiers, E. Toby
Toju, Hirokazu
Facilitative interaction networks in experimental microbial community dynamics
title Facilitative interaction networks in experimental microbial community dynamics
title_full Facilitative interaction networks in experimental microbial community dynamics
title_fullStr Facilitative interaction networks in experimental microbial community dynamics
title_full_unstemmed Facilitative interaction networks in experimental microbial community dynamics
title_short Facilitative interaction networks in experimental microbial community dynamics
title_sort facilitative interaction networks in experimental microbial community dynamics
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126487/
https://www.ncbi.nlm.nih.gov/pubmed/37113242
http://dx.doi.org/10.3389/fmicb.2023.1153952
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