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Chemosynthetic and photosynthetic bacteria contribute differentially to primary production across a steep desert aridity gradient

Desert soils harbour diverse communities of aerobic bacteria despite lacking substantial organic carbon inputs from vegetation. A major question is therefore how these communities maintain their biodiversity and biomass in these resource-limiting ecosystems. Here, we investigated desert topsoils and...

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Autores principales: Bay, Sean K., Waite, David W., Dong, Xiyang, Gillor, Osnat, Chown, Steven L., Hugenholtz, Philip, Greening, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528921/
https://www.ncbi.nlm.nih.gov/pubmed/34035443
http://dx.doi.org/10.1038/s41396-021-01001-0
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author Bay, Sean K.
Waite, David W.
Dong, Xiyang
Gillor, Osnat
Chown, Steven L.
Hugenholtz, Philip
Greening, Chris
author_facet Bay, Sean K.
Waite, David W.
Dong, Xiyang
Gillor, Osnat
Chown, Steven L.
Hugenholtz, Philip
Greening, Chris
author_sort Bay, Sean K.
collection PubMed
description Desert soils harbour diverse communities of aerobic bacteria despite lacking substantial organic carbon inputs from vegetation. A major question is therefore how these communities maintain their biodiversity and biomass in these resource-limiting ecosystems. Here, we investigated desert topsoils and biological soil crusts collected along an aridity gradient traversing four climatic regions (sub-humid, semi-arid, arid, and hyper-arid). Metagenomic analysis indicated these communities vary in their capacity to use sunlight, organic compounds, and inorganic compounds as energy sources. Thermoleophilia, Actinobacteria, and Acidimicrobiia were the most abundant and prevalent bacterial classes across the aridity gradient in both topsoils and biocrusts. Contrary to the classical view that these taxa are obligate organoheterotrophs, genome-resolved analysis suggested they are metabolically flexible, with the capacity to also use atmospheric H(2) to support aerobic respiration and often carbon fixation. In contrast, Cyanobacteria were patchily distributed and only abundant in certain biocrusts. Activity measurements profiled how aerobic H(2) oxidation, chemosynthetic CO(2) fixation, and photosynthesis varied with aridity. Cell-specific rates of atmospheric H(2) consumption increased 143-fold along the aridity gradient, correlating with increased abundance of high-affinity hydrogenases. Photosynthetic and chemosynthetic primary production co-occurred throughout the gradient, with photosynthesis dominant in biocrusts and chemosynthesis dominant in arid and hyper-arid soils. Altogether, these findings suggest that the major bacterial lineages inhabiting hot deserts use different strategies for energy and carbon acquisition depending on resource availability. Moreover, they highlight the previously overlooked roles of Actinobacteriota as abundant primary producers and trace gases as critical energy sources supporting productivity and resilience of desert ecosystems.
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spelling pubmed-85289212021-10-22 Chemosynthetic and photosynthetic bacteria contribute differentially to primary production across a steep desert aridity gradient Bay, Sean K. Waite, David W. Dong, Xiyang Gillor, Osnat Chown, Steven L. Hugenholtz, Philip Greening, Chris ISME J Article Desert soils harbour diverse communities of aerobic bacteria despite lacking substantial organic carbon inputs from vegetation. A major question is therefore how these communities maintain their biodiversity and biomass in these resource-limiting ecosystems. Here, we investigated desert topsoils and biological soil crusts collected along an aridity gradient traversing four climatic regions (sub-humid, semi-arid, arid, and hyper-arid). Metagenomic analysis indicated these communities vary in their capacity to use sunlight, organic compounds, and inorganic compounds as energy sources. Thermoleophilia, Actinobacteria, and Acidimicrobiia were the most abundant and prevalent bacterial classes across the aridity gradient in both topsoils and biocrusts. Contrary to the classical view that these taxa are obligate organoheterotrophs, genome-resolved analysis suggested they are metabolically flexible, with the capacity to also use atmospheric H(2) to support aerobic respiration and often carbon fixation. In contrast, Cyanobacteria were patchily distributed and only abundant in certain biocrusts. Activity measurements profiled how aerobic H(2) oxidation, chemosynthetic CO(2) fixation, and photosynthesis varied with aridity. Cell-specific rates of atmospheric H(2) consumption increased 143-fold along the aridity gradient, correlating with increased abundance of high-affinity hydrogenases. Photosynthetic and chemosynthetic primary production co-occurred throughout the gradient, with photosynthesis dominant in biocrusts and chemosynthesis dominant in arid and hyper-arid soils. Altogether, these findings suggest that the major bacterial lineages inhabiting hot deserts use different strategies for energy and carbon acquisition depending on resource availability. Moreover, they highlight the previously overlooked roles of Actinobacteriota as abundant primary producers and trace gases as critical energy sources supporting productivity and resilience of desert ecosystems. Nature Publishing Group UK 2021-05-25 2021-11 /pmc/articles/PMC8528921/ /pubmed/34035443 http://dx.doi.org/10.1038/s41396-021-01001-0 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
Bay, Sean K.
Waite, David W.
Dong, Xiyang
Gillor, Osnat
Chown, Steven L.
Hugenholtz, Philip
Greening, Chris
Chemosynthetic and photosynthetic bacteria contribute differentially to primary production across a steep desert aridity gradient
title Chemosynthetic and photosynthetic bacteria contribute differentially to primary production across a steep desert aridity gradient
title_full Chemosynthetic and photosynthetic bacteria contribute differentially to primary production across a steep desert aridity gradient
title_fullStr Chemosynthetic and photosynthetic bacteria contribute differentially to primary production across a steep desert aridity gradient
title_full_unstemmed Chemosynthetic and photosynthetic bacteria contribute differentially to primary production across a steep desert aridity gradient
title_short Chemosynthetic and photosynthetic bacteria contribute differentially to primary production across a steep desert aridity gradient
title_sort chemosynthetic and photosynthetic bacteria contribute differentially to primary production across a steep desert aridity gradient
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528921/
https://www.ncbi.nlm.nih.gov/pubmed/34035443
http://dx.doi.org/10.1038/s41396-021-01001-0
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