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The soil microbial food web revisited: Predatory myxobacteria as keystone taxa?
Trophic interactions are crucial for carbon cycling in food webs. Traditionally, eukaryotic micropredators are considered the major micropredators of bacteria in soils, although bacteria like myxobacteria and Bdellovibrio are also known bacterivores. Until recently, it was impossible to assess the a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397742/ https://www.ncbi.nlm.nih.gov/pubmed/33746204 http://dx.doi.org/10.1038/s41396-021-00958-2 |
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author | Petters, Sebastian Groß, Verena Söllinger, Andrea Pichler, Michelle Reinhard, Anne Bengtsson, Mia Maria Urich, Tim |
author_facet | Petters, Sebastian Groß, Verena Söllinger, Andrea Pichler, Michelle Reinhard, Anne Bengtsson, Mia Maria Urich, Tim |
author_sort | Petters, Sebastian |
collection | PubMed |
description | Trophic interactions are crucial for carbon cycling in food webs. Traditionally, eukaryotic micropredators are considered the major micropredators of bacteria in soils, although bacteria like myxobacteria and Bdellovibrio are also known bacterivores. Until recently, it was impossible to assess the abundance of prokaryotes and eukaryotes in soil food webs simultaneously. Using metatranscriptomic three-domain community profiling we identified pro- and eukaryotic micropredators in 11 European mineral and organic soils from different climes. Myxobacteria comprised 1.5–9.7% of all obtained SSU rRNA transcripts and more than 60% of all identified potential bacterivores in most soils. The name-giving and well-characterized predatory bacteria affiliated with the Myxococcaceae were barely present, while Haliangiaceae and Polyangiaceae dominated. In predation assays, representatives of the latter showed prey spectra as broad as the Myxococcaceae. 18S rRNA transcripts from eukaryotic micropredators, like amoeba and nematodes, were generally less abundant than myxobacterial 16S rRNA transcripts, especially in mineral soils. Although SSU rRNA does not directly reflect organismic abundance, our findings indicate that myxobacteria could be keystone taxa in the soil microbial food web, with potential impact on prokaryotic community composition. Further, they suggest an overlooked, yet ecologically relevant food web module, independent of eukaryotic micropredators and subject to separate environmental and evolutionary pressures. |
format | Online Article Text |
id | pubmed-8397742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83977422021-09-15 The soil microbial food web revisited: Predatory myxobacteria as keystone taxa? Petters, Sebastian Groß, Verena Söllinger, Andrea Pichler, Michelle Reinhard, Anne Bengtsson, Mia Maria Urich, Tim ISME J Article Trophic interactions are crucial for carbon cycling in food webs. Traditionally, eukaryotic micropredators are considered the major micropredators of bacteria in soils, although bacteria like myxobacteria and Bdellovibrio are also known bacterivores. Until recently, it was impossible to assess the abundance of prokaryotes and eukaryotes in soil food webs simultaneously. Using metatranscriptomic three-domain community profiling we identified pro- and eukaryotic micropredators in 11 European mineral and organic soils from different climes. Myxobacteria comprised 1.5–9.7% of all obtained SSU rRNA transcripts and more than 60% of all identified potential bacterivores in most soils. The name-giving and well-characterized predatory bacteria affiliated with the Myxococcaceae were barely present, while Haliangiaceae and Polyangiaceae dominated. In predation assays, representatives of the latter showed prey spectra as broad as the Myxococcaceae. 18S rRNA transcripts from eukaryotic micropredators, like amoeba and nematodes, were generally less abundant than myxobacterial 16S rRNA transcripts, especially in mineral soils. Although SSU rRNA does not directly reflect organismic abundance, our findings indicate that myxobacteria could be keystone taxa in the soil microbial food web, with potential impact on prokaryotic community composition. Further, they suggest an overlooked, yet ecologically relevant food web module, independent of eukaryotic micropredators and subject to separate environmental and evolutionary pressures. Nature Publishing Group UK 2021-03-21 2021-09 /pmc/articles/PMC8397742/ /pubmed/33746204 http://dx.doi.org/10.1038/s41396-021-00958-2 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 Petters, Sebastian Groß, Verena Söllinger, Andrea Pichler, Michelle Reinhard, Anne Bengtsson, Mia Maria Urich, Tim The soil microbial food web revisited: Predatory myxobacteria as keystone taxa? |
title | The soil microbial food web revisited: Predatory myxobacteria as keystone taxa? |
title_full | The soil microbial food web revisited: Predatory myxobacteria as keystone taxa? |
title_fullStr | The soil microbial food web revisited: Predatory myxobacteria as keystone taxa? |
title_full_unstemmed | The soil microbial food web revisited: Predatory myxobacteria as keystone taxa? |
title_short | The soil microbial food web revisited: Predatory myxobacteria as keystone taxa? |
title_sort | soil microbial food web revisited: predatory myxobacteria as keystone taxa? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397742/ https://www.ncbi.nlm.nih.gov/pubmed/33746204 http://dx.doi.org/10.1038/s41396-021-00958-2 |
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