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Community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems

A fundamental question in community ecology is the role of predator–prey interactions in food-web stability and species coexistence. Although microbial microcosms offer powerful systems to investigate it, interrogating the environment is much more arduous. Here, we show in a 1-year survey that the o...

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Autores principales: Cohen, Yossi, Pasternak, Zohar, Müller, Susann, Hübschmann, Thomas, Schattenberg, Florian, Sivakala, Kunjukrishnan Kamalakshi, Abed-Rabbo, Alfred, Chatzinotas, Antonis, Jurkevitch, Edouard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446003/
https://www.ncbi.nlm.nih.gov/pubmed/34531395
http://dx.doi.org/10.1038/s41467-021-25824-9
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author Cohen, Yossi
Pasternak, Zohar
Müller, Susann
Hübschmann, Thomas
Schattenberg, Florian
Sivakala, Kunjukrishnan Kamalakshi
Abed-Rabbo, Alfred
Chatzinotas, Antonis
Jurkevitch, Edouard
author_facet Cohen, Yossi
Pasternak, Zohar
Müller, Susann
Hübschmann, Thomas
Schattenberg, Florian
Sivakala, Kunjukrishnan Kamalakshi
Abed-Rabbo, Alfred
Chatzinotas, Antonis
Jurkevitch, Edouard
author_sort Cohen, Yossi
collection PubMed
description A fundamental question in community ecology is the role of predator–prey interactions in food-web stability and species coexistence. Although microbial microcosms offer powerful systems to investigate it, interrogating the environment is much more arduous. Here, we show in a 1-year survey that the obligate predators Bdellovibrio and like organisms (BALOs) can regulate prey populations, possibly in a density-dependent manner, in the naturally complex, species-rich environments of wastewater treatment plants. Abundant as well as rarer prey populations are affected, leading to an oscillating predatory landscape shifting at various temporal scales in which the total population remains stable. Shifts, along with differential prey range, explain co-existence of the numerous predators through niche partitioning. We validate these sequence-based findings using single-cell sorting combined with fluorescent hybridization and community sequencing. Our approach should be applicable for deciphering community interactions in other systems.
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spelling pubmed-84460032021-10-04 Community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems Cohen, Yossi Pasternak, Zohar Müller, Susann Hübschmann, Thomas Schattenberg, Florian Sivakala, Kunjukrishnan Kamalakshi Abed-Rabbo, Alfred Chatzinotas, Antonis Jurkevitch, Edouard Nat Commun Article A fundamental question in community ecology is the role of predator–prey interactions in food-web stability and species coexistence. Although microbial microcosms offer powerful systems to investigate it, interrogating the environment is much more arduous. Here, we show in a 1-year survey that the obligate predators Bdellovibrio and like organisms (BALOs) can regulate prey populations, possibly in a density-dependent manner, in the naturally complex, species-rich environments of wastewater treatment plants. Abundant as well as rarer prey populations are affected, leading to an oscillating predatory landscape shifting at various temporal scales in which the total population remains stable. Shifts, along with differential prey range, explain co-existence of the numerous predators through niche partitioning. We validate these sequence-based findings using single-cell sorting combined with fluorescent hybridization and community sequencing. Our approach should be applicable for deciphering community interactions in other systems. Nature Publishing Group UK 2021-09-16 /pmc/articles/PMC8446003/ /pubmed/34531395 http://dx.doi.org/10.1038/s41467-021-25824-9 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
Cohen, Yossi
Pasternak, Zohar
Müller, Susann
Hübschmann, Thomas
Schattenberg, Florian
Sivakala, Kunjukrishnan Kamalakshi
Abed-Rabbo, Alfred
Chatzinotas, Antonis
Jurkevitch, Edouard
Community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems
title Community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems
title_full Community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems
title_fullStr Community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems
title_full_unstemmed Community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems
title_short Community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems
title_sort community and single cell analyses reveal complex predatory interactions between bacteria in high diversity systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446003/
https://www.ncbi.nlm.nih.gov/pubmed/34531395
http://dx.doi.org/10.1038/s41467-021-25824-9
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