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Bacterial aerobic methane cycling by the marine sponge-associated microbiome
BACKGROUND: Methanotrophy by the sponge-hosted microbiome has been mainly reported in the ecological context of deep-sea hydrocarbon seep niches where methane is either produced geothermically or via anaerobic methanogenic archaea inhabiting the sulfate-depleted sediments. However, methane-oxidizing...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999580/ https://www.ncbi.nlm.nih.gov/pubmed/36899421 http://dx.doi.org/10.1186/s40168-023-01467-4 |
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author | Ramírez, Gustavo A. Bar-Shalom, Rinat Furlan, Andrea Romeo, Roberto Gavagnin, Michelle Calabrese, Gianluca Garber, Arkadiy I. Steindler, Laura |
author_facet | Ramírez, Gustavo A. Bar-Shalom, Rinat Furlan, Andrea Romeo, Roberto Gavagnin, Michelle Calabrese, Gianluca Garber, Arkadiy I. Steindler, Laura |
author_sort | Ramírez, Gustavo A. |
collection | PubMed |
description | BACKGROUND: Methanotrophy by the sponge-hosted microbiome has been mainly reported in the ecological context of deep-sea hydrocarbon seep niches where methane is either produced geothermically or via anaerobic methanogenic archaea inhabiting the sulfate-depleted sediments. However, methane-oxidizing bacteria from the candidate phylum Binatota have recently been described and shown to be present in oxic shallow-water marine sponges, where sources of methane remain undescribed. RESULTS: Here, using an integrative -omics approach, we provide evidence for sponge-hosted bacterial methane synthesis occurring in fully oxygenated shallow-water habitats. Specifically, we suggest methane generation occurs via at least two independent pathways involving methylamine and methylphosphonate transformations that, concomitantly to aerobic methane production, generate bioavailable nitrogen and phosphate, respectively. Methylphosphonate may be sourced from seawater continuously filtered by the sponge host. Methylamines may also be externally sourced or, alternatively, generated by a multi-step metabolic process where carnitine, derived from sponge cell debris, is transformed to methylamine by different sponge-hosted microbial lineages. Finally, methanotrophs specialized in pigment production, affiliated to the phylum Binatota, may provide a photoprotective function, closing a previously undescribed C(1)-metabolic loop that involves both the sponge host and specific members of the associated microbial community. CONCLUSION: Given the global distribution of this ancient animal lineage and their remarkable water filtration activity, sponge-hosted methane cycling may affect methane supersaturation in oxic coastal environments. Depending on the net balance between methane production and consumption, sponges may serve as marine sources or sinks of this potent greenhouse gas. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01467-4. |
format | Online Article Text |
id | pubmed-9999580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99995802023-03-11 Bacterial aerobic methane cycling by the marine sponge-associated microbiome Ramírez, Gustavo A. Bar-Shalom, Rinat Furlan, Andrea Romeo, Roberto Gavagnin, Michelle Calabrese, Gianluca Garber, Arkadiy I. Steindler, Laura Microbiome Research BACKGROUND: Methanotrophy by the sponge-hosted microbiome has been mainly reported in the ecological context of deep-sea hydrocarbon seep niches where methane is either produced geothermically or via anaerobic methanogenic archaea inhabiting the sulfate-depleted sediments. However, methane-oxidizing bacteria from the candidate phylum Binatota have recently been described and shown to be present in oxic shallow-water marine sponges, where sources of methane remain undescribed. RESULTS: Here, using an integrative -omics approach, we provide evidence for sponge-hosted bacterial methane synthesis occurring in fully oxygenated shallow-water habitats. Specifically, we suggest methane generation occurs via at least two independent pathways involving methylamine and methylphosphonate transformations that, concomitantly to aerobic methane production, generate bioavailable nitrogen and phosphate, respectively. Methylphosphonate may be sourced from seawater continuously filtered by the sponge host. Methylamines may also be externally sourced or, alternatively, generated by a multi-step metabolic process where carnitine, derived from sponge cell debris, is transformed to methylamine by different sponge-hosted microbial lineages. Finally, methanotrophs specialized in pigment production, affiliated to the phylum Binatota, may provide a photoprotective function, closing a previously undescribed C(1)-metabolic loop that involves both the sponge host and specific members of the associated microbial community. CONCLUSION: Given the global distribution of this ancient animal lineage and their remarkable water filtration activity, sponge-hosted methane cycling may affect methane supersaturation in oxic coastal environments. Depending on the net balance between methane production and consumption, sponges may serve as marine sources or sinks of this potent greenhouse gas. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01467-4. BioMed Central 2023-03-10 /pmc/articles/PMC9999580/ /pubmed/36899421 http://dx.doi.org/10.1186/s40168-023-01467-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ramírez, Gustavo A. Bar-Shalom, Rinat Furlan, Andrea Romeo, Roberto Gavagnin, Michelle Calabrese, Gianluca Garber, Arkadiy I. Steindler, Laura Bacterial aerobic methane cycling by the marine sponge-associated microbiome |
title | Bacterial aerobic methane cycling by the marine sponge-associated microbiome |
title_full | Bacterial aerobic methane cycling by the marine sponge-associated microbiome |
title_fullStr | Bacterial aerobic methane cycling by the marine sponge-associated microbiome |
title_full_unstemmed | Bacterial aerobic methane cycling by the marine sponge-associated microbiome |
title_short | Bacterial aerobic methane cycling by the marine sponge-associated microbiome |
title_sort | bacterial aerobic methane cycling by the marine sponge-associated microbiome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999580/ https://www.ncbi.nlm.nih.gov/pubmed/36899421 http://dx.doi.org/10.1186/s40168-023-01467-4 |
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