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Coordination and divergence in community assembly processes across co-occurring microbial groups separated by cell size

Setting the pace of life and constraining the role of members in food webs, body size can affect the structure and dynamics of communities across multiple scales of biological organization (e.g., from the individual to the ecosystem). However, its effects on shaping microbial communities, as well as...

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Autores principales: Li, Xinghao, Stegen, James C., Yu, Yuhe, Huang, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272581/
https://www.ncbi.nlm.nih.gov/pubmed/37333654
http://dx.doi.org/10.3389/fmicb.2023.1166322
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author Li, Xinghao
Stegen, James C.
Yu, Yuhe
Huang, Jie
author_facet Li, Xinghao
Stegen, James C.
Yu, Yuhe
Huang, Jie
author_sort Li, Xinghao
collection PubMed
description Setting the pace of life and constraining the role of members in food webs, body size can affect the structure and dynamics of communities across multiple scales of biological organization (e.g., from the individual to the ecosystem). However, its effects on shaping microbial communities, as well as underlying assembly processes, remain poorly known. Here, we analyzed microbial diversity in the largest urban lake in China and disentangled the ecological processes governing microbial eukaryotes and prokaryotes using 16S and 18S amplicon sequencing. We found that pico/nano-eukaryotes (0.22−20 μm) and micro-eukaryotes (20−200 μm) showed significant differences in terms of both community composition and assembly processes even though they were characterized by similar phylotype diversity. We also found scale dependencies whereby micro-eukaryotes were strongly governed by environmental selection at the local scale and dispersal limitation at the regional scale. Interestingly, it was the micro-eukaryotes, rather than the pico/nano-eukaryotes, that shared similar distribution and community assembly patterns with the prokaryotes. This indicated that assembly processes of eukaryotes may be coupled or decoupled from prokaryotes’ assembly processes based on eukaryote cell size. While the results support the important influence of cell size, there may be other factors leading to different levels of assembly process coupling across size classes. Additional studies are needed to quantitatively parse the influence of cell size versus other factors as drivers of coordinated and divergent community assembly processes across microbial groups. Regardless of the governing mechanisms, our results show that there are clear patterns in how assembly processes are coupled across sub-communities defined by cell size. These size-structured patterns could be used to help predict shifts in microbial food webs in response to future disturbance.
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spelling pubmed-102725812023-06-17 Coordination and divergence in community assembly processes across co-occurring microbial groups separated by cell size Li, Xinghao Stegen, James C. Yu, Yuhe Huang, Jie Front Microbiol Microbiology Setting the pace of life and constraining the role of members in food webs, body size can affect the structure and dynamics of communities across multiple scales of biological organization (e.g., from the individual to the ecosystem). However, its effects on shaping microbial communities, as well as underlying assembly processes, remain poorly known. Here, we analyzed microbial diversity in the largest urban lake in China and disentangled the ecological processes governing microbial eukaryotes and prokaryotes using 16S and 18S amplicon sequencing. We found that pico/nano-eukaryotes (0.22−20 μm) and micro-eukaryotes (20−200 μm) showed significant differences in terms of both community composition and assembly processes even though they were characterized by similar phylotype diversity. We also found scale dependencies whereby micro-eukaryotes were strongly governed by environmental selection at the local scale and dispersal limitation at the regional scale. Interestingly, it was the micro-eukaryotes, rather than the pico/nano-eukaryotes, that shared similar distribution and community assembly patterns with the prokaryotes. This indicated that assembly processes of eukaryotes may be coupled or decoupled from prokaryotes’ assembly processes based on eukaryote cell size. While the results support the important influence of cell size, there may be other factors leading to different levels of assembly process coupling across size classes. Additional studies are needed to quantitatively parse the influence of cell size versus other factors as drivers of coordinated and divergent community assembly processes across microbial groups. Regardless of the governing mechanisms, our results show that there are clear patterns in how assembly processes are coupled across sub-communities defined by cell size. These size-structured patterns could be used to help predict shifts in microbial food webs in response to future disturbance. Frontiers Media S.A. 2023-06-02 /pmc/articles/PMC10272581/ /pubmed/37333654 http://dx.doi.org/10.3389/fmicb.2023.1166322 Text en Copyright © 2023 Li, Stegen, Yu and Huang. 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
Li, Xinghao
Stegen, James C.
Yu, Yuhe
Huang, Jie
Coordination and divergence in community assembly processes across co-occurring microbial groups separated by cell size
title Coordination and divergence in community assembly processes across co-occurring microbial groups separated by cell size
title_full Coordination and divergence in community assembly processes across co-occurring microbial groups separated by cell size
title_fullStr Coordination and divergence in community assembly processes across co-occurring microbial groups separated by cell size
title_full_unstemmed Coordination and divergence in community assembly processes across co-occurring microbial groups separated by cell size
title_short Coordination and divergence in community assembly processes across co-occurring microbial groups separated by cell size
title_sort coordination and divergence in community assembly processes across co-occurring microbial groups separated by cell size
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272581/
https://www.ncbi.nlm.nih.gov/pubmed/37333654
http://dx.doi.org/10.3389/fmicb.2023.1166322
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