Microbial aerotrophy enables continuous primary production in diverse cave ecosystems.

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Autori principali: Bay, Sean K, Ni, Gaofeng, Lappan, Rachael, Leung, Pok Man, Wong, Wei Wen, Ry Holland, S I, Athukorala, Nadeesha, Knudsen, Kalinka Sand, Fan, Ziqi, Kerou, Melina, Jain, Surbhi, Schmidt, Oliver, Eate, Vera, Clarke, David A, Jirapanjawat, Thanavit, Tveit, Alexander, Featonby, Tim, White, Susan, White, Nicholas, McGeoch, Melodie A, Singleton, Caitlin M, Cook, Perran L M, Chown, Steven L, Greening, Chris
Natura: Artículo científico
Lingua:en
Pubblicazione: Nature communications 2025
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author Bay, Sean K
Ni, Gaofeng
Lappan, Rachael
Leung, Pok Man
Wong, Wei Wen
Ry Holland, S I
Athukorala, Nadeesha
Knudsen, Kalinka Sand
Fan, Ziqi
Kerou, Melina
Jain, Surbhi
Schmidt, Oliver
Eate, Vera
Clarke, David A
Jirapanjawat, Thanavit
Tveit, Alexander
Featonby, Tim
White, Susan
White, Nicholas
McGeoch, Melodie A
Singleton, Caitlin M
Cook, Perran L M
Chown, Steven L
Greening, Chris
author_facet Bay, Sean K
Ni, Gaofeng
Lappan, Rachael
Leung, Pok Man
Wong, Wei Wen
Ry Holland, S I
Athukorala, Nadeesha
Knudsen, Kalinka Sand
Fan, Ziqi
Kerou, Melina
Jain, Surbhi
Schmidt, Oliver
Eate, Vera
Clarke, David A
Jirapanjawat, Thanavit
Tveit, Alexander
Featonby, Tim
White, Susan
White, Nicholas
McGeoch, Melodie A
Singleton, Caitlin M
Cook, Perran L M
Chown, Steven L
Greening, Chris
Bay, Sean K
Ni, Gaofeng
Lappan, Rachael
Leung, Pok Man
Wong, Wei Wen
Ry Holland, S I
Athukorala, Nadeesha
Knudsen, Kalinka Sand
Fan, Ziqi
Kerou, Melina
Jain, Surbhi
Schmidt, Oliver
Eate, Vera
Clarke, David A
Jirapanjawat, Thanavit
Tveit, Alexander
Featonby, Tim
White, Susan
White, Nicholas
McGeoch, Melodie A
Singleton, Caitlin M
Cook, Perran L M
Chown, Steven L
Greening, Chris
collection PubMed - marine biology
contents Microbial aerotrophy enables continuous primary production in diverse cave ecosystems. Bay, Sean K Ni, Gaofeng Lappan, Rachael Leung, Pok Man Wong, Wei Wen Ry Holland, S I Athukorala, Nadeesha Knudsen, Kalinka Sand Fan, Ziqi Kerou, Melina Jain, Surbhi Schmidt, Oliver Eate, Vera Clarke, David A Jirapanjawat, Thanavit Tveit, Alexander Featonby, Tim White, Susan White, Nicholas McGeoch, Melodie A Singleton, Caitlin M Cook, Perran L M Chown, Steven L Greening, Chris Caves Ecosystem Carbon Dioxide Metagenome Geologic Sediments Microbiota Hydrogen Metagenomics Bacteria Biodiversity Carbon Monoxide Biofilms Gammaproteobacteria Aerated caves receive minimal light energy, yet host diverse microbial communities and the strategies allowing them to meet energy and carbon needs remain unclear. We determined the processes and mediators of primary production in aerated limestone and basalt caves through paired metagenomic and biogeochemical profiling. Four caves were sampled, including sediments and biofilms, yielding 94 metagenomes. Based on 1458 metagenome-assembled genomes, over half of microbial cells encode enzymes to use atmospheric trace gases as energy and carbon sources. The most abundant microbes are chemosynthetic primary producers, notably the gammaproteobacterial methanotrophic order Ca. Methylocavales and two uncultivated actinobacterial genera predicted to grow on atmospheric hydrogen, carbon dioxide, and carbon monoxide. Biogeochemical and isotopic measurements confirmed that these gases are rapidly consumed at rates likely sustaining a substantial fraction of the community and potentially driving primary production. Conventional chemolithoautotrophs, using ammonium and sulfide, are also enriched and active. Altogether, these results indicate that caves are unique in microbial biodiversity and the biogeochemical processes sustaining them. Consumption of atmospheric trace gases likely has a dual role in caves, providing energy for microbial survival and potentially supporting chemosynthetic growth, thereby introducing organic carbon. This process, defined as 'aerotrophy', operates alongside organic and inorganic inputs.
format Artículo científico
id pubmed_41271709
institution PubMed
language en
publishDate 2025
publisher Nature communications
record_format pubmed
spellingShingle Microbial aerotrophy enables continuous primary production in diverse cave ecosystems.
Bay, Sean K
Ni, Gaofeng
Lappan, Rachael
Leung, Pok Man
Wong, Wei Wen
Ry Holland, S I
Athukorala, Nadeesha
Knudsen, Kalinka Sand
Fan, Ziqi
Kerou, Melina
Jain, Surbhi
Schmidt, Oliver
Eate, Vera
Clarke, David A
Jirapanjawat, Thanavit
Tveit, Alexander
Featonby, Tim
White, Susan
White, Nicholas
McGeoch, Melodie A
Singleton, Caitlin M
Cook, Perran L M
Chown, Steven L
Greening, Chris
Caves
Ecosystem
Carbon Dioxide
Metagenome
Geologic Sediments
Microbiota
Hydrogen
Metagenomics
Bacteria
Biodiversity
Carbon Monoxide
Biofilms
Gammaproteobacteria
Microbial aerotrophy enables continuous primary production in diverse cave ecosystems. Bay, Sean K Ni, Gaofeng Lappan, Rachael Leung, Pok Man Wong, Wei Wen Ry Holland, S I Athukorala, Nadeesha Knudsen, Kalinka Sand Fan, Ziqi Kerou, Melina Jain, Surbhi Schmidt, Oliver Eate, Vera Clarke, David A Jirapanjawat, Thanavit Tveit, Alexander Featonby, Tim White, Susan White, Nicholas McGeoch, Melodie A Singleton, Caitlin M Cook, Perran L M Chown, Steven L Greening, Chris Caves Ecosystem Carbon Dioxide Metagenome Geologic Sediments Microbiota Hydrogen Metagenomics Bacteria Biodiversity Carbon Monoxide Biofilms Gammaproteobacteria Aerated caves receive minimal light energy, yet host diverse microbial communities and the strategies allowing them to meet energy and carbon needs remain unclear. We determined the processes and mediators of primary production in aerated limestone and basalt caves through paired metagenomic and biogeochemical profiling. Four caves were sampled, including sediments and biofilms, yielding 94 metagenomes. Based on 1458 metagenome-assembled genomes, over half of microbial cells encode enzymes to use atmospheric trace gases as energy and carbon sources. The most abundant microbes are chemosynthetic primary producers, notably the gammaproteobacterial methanotrophic order Ca. Methylocavales and two uncultivated actinobacterial genera predicted to grow on atmospheric hydrogen, carbon dioxide, and carbon monoxide. Biogeochemical and isotopic measurements confirmed that these gases are rapidly consumed at rates likely sustaining a substantial fraction of the community and potentially driving primary production. Conventional chemolithoautotrophs, using ammonium and sulfide, are also enriched and active. Altogether, these results indicate that caves are unique in microbial biodiversity and the biogeochemical processes sustaining them. Consumption of atmospheric trace gases likely has a dual role in caves, providing energy for microbial survival and potentially supporting chemosynthetic growth, thereby introducing organic carbon. This process, defined as 'aerotrophy', operates alongside organic and inorganic inputs.
title Microbial aerotrophy enables continuous primary production in diverse cave ecosystems.
topic Caves
Ecosystem
Carbon Dioxide
Metagenome
Geologic Sediments
Microbiota
Hydrogen
Metagenomics
Bacteria
Biodiversity
Carbon Monoxide
Biofilms
Gammaproteobacteria
url https://pubmed.ncbi.nlm.nih.gov/41271709/