Covariation of hot spring geochemistry with microbial genomic diversity, function, and evolution

The geosphere and the microbial biosphere have co-evolved for ~3.8 Ga, with many lines of evidence suggesting a hydrothermal habitat for life's origin. However, the extent that contemporary thermophiles and their hydrothermal habitats reflect those that likely existed on early Earth remains unknown. To address this knowledge gap, 64 geochemical analytes were measured and 1022 metagenome-assembled-genomes (MAGs) were generated from 34 chemosynthetic high-temperature springs in Yellowstone National Park and analysed alongside 444 MAGs from 35 published metagenomes. We used these data to evaluate co-variation in MAG taxonomy, metabolism, and phylogeny as a function of hot spring geochemistry. We found that cohorts of MAGs and their functions are discretely distributed across pH gradients that reflect different geochemical provinces. Acidic or circumneutral/alkaline springs harbor MAGs that branched later and are enriched in sulfur- and arsenic-based O<sub>2</sub>-dependent metabolic pathways that are inconsistent with early Earth conditions. In contrast, moderately acidic springs sourced by volcanic gas harbor earlier-branching MAGs that are enriched in anaerobic, gas-dependent metabolisms (e.g. H<sub>2</sub>, CO<sub>2</sub>, CH<sub>4</sub> metabolism) that have been hypothesized to support early microbial life. Our results provide insight into the influence of redox state in the eco-evolutionary feedbacks between thermophiles and their habitats and suggest moderately acidic springs as early Earth analogs.

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Publication Details

Journal
Nature Communications
Published
2024-08-29
DOI
https://doi.org/10.1038/s41467-024-51841-5
Citations
23
Primary Topic
Microbial Community Ecology and Physiology
Type
article
Field-Weighted Citation Impact
10.55

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article

Covariation of hot spring geochemistry with microbial genomic diversity, function, and evolution

Daniel R. Colman, Lisa M. Keller, Anna Shoemaker, Eric S. Boyd et al.
23 citations
Nature Communications
Microbial Community Ecology and Physiology
10.55
article

Covariation of hot spring geochemistry with microbial genomic diversity, function, and evolution

Daniel R. Colman, Lisa M. Keller, Anna Shoemaker, Eric S. Boyd, Brian St. Clair, Eva Andrade‐Barahona, Alysia Cox, Emilia Arteaga-Pozo
article en
23 citations

Abstract

The geosphere and the microbial biosphere have co-evolved for ~3.8 Ga, with many lines of evidence suggesting a hydrothermal habitat for life's origin. However, the extent that contemporary thermophiles and their hydrothermal habitats reflect those that likely existed on early Earth remains unknown. To address this knowledge gap, 64 geochemical analytes were measured and 1022 metagenome-assembled-genomes (MAGs) were generated from 34 chemosynthetic high-temperature springs in Yellowstone National Park and analysed alongside 444 MAGs from 35 published metagenomes. We used these data to evaluate co-variation in MAG taxonomy, metabolism, and phylogeny as a function of hot spring geochemistry. We found that cohorts of MAGs and their functions are discretely distributed across pH gradients that reflect different geochemical provinces. Acidic or circumneutral/alkaline springs harbor MAGs that branched later and are enriched in sulfur- and arsenic-based O<sub>2</sub>-dependent metabolic pathways that are inconsistent with early Earth conditions. In contrast, moderately acidic springs sourced by volcanic gas harbor earlier-branching MAGs that are enriched in anaerobic, gas-dependent metabolisms (e.g. H<sub>2</sub>, CO<sub>2</sub>, CH<sub>4</sub> metabolism) that have been hypothesized to support early microbial life. Our results provide insight into the influence of redox state in the eco-evolutionary feedbacks between thermophiles and their habitats and suggest moderately acidic springs as early Earth analogs.

Nature CommunicationsVol. 15(1)
Montana State University (US), Montana Technological University (US)
U.S. Department of Energy, National Aeronautics and Space Administration, Joint Genome Institute, Nuclear Safety and Security Commission, National Park Service
Openalex Percentile: Top 1%
Microbial Community Ecology and Physiology
10.55
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