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Competition-cooperation in the chemoautotrophic ecosystem of Movile Cave: first metagenomic approach on sediments
BACKGROUND: Movile Cave (SE Romania) is a chemoautotrophically-based ecosystem fed by hydrogen sulfide-rich groundwater serving as a primary energy source analogous to the deep-sea hydrothermal ecosystems. Our current understanding of Movile Cave microbiology has been confined to the sulfidic water...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386943/ https://www.ncbi.nlm.nih.gov/pubmed/35978381 http://dx.doi.org/10.1186/s40793-022-00438-w |
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author | Chiciudean, Iulia Russo, Giancarlo Bogdan, Diana Felicia Levei, Erika Andrea Faur, Luchiana Hillebrand-Voiculescu, Alexandra Moldovan, Oana Teodora Banciu, Horia Leonard |
author_facet | Chiciudean, Iulia Russo, Giancarlo Bogdan, Diana Felicia Levei, Erika Andrea Faur, Luchiana Hillebrand-Voiculescu, Alexandra Moldovan, Oana Teodora Banciu, Horia Leonard |
author_sort | Chiciudean, Iulia |
collection | PubMed |
description | BACKGROUND: Movile Cave (SE Romania) is a chemoautotrophically-based ecosystem fed by hydrogen sulfide-rich groundwater serving as a primary energy source analogous to the deep-sea hydrothermal ecosystems. Our current understanding of Movile Cave microbiology has been confined to the sulfidic water and its proximity, as most studies focused on the water-floating microbial mat and planktonic accumulations likely acting as the primary production powerhouse of this unique subterranean ecosystem. By employing comprehensive genomic-resolved metagenomics, we questioned the spatial variation, chemoautotrophic abilities, ecological interactions and trophic roles of Movile Cave’s microbiome thriving beyond the sulfidic-rich water. RESULTS: A customized bioinformatics pipeline led to the recovery of 106 high-quality metagenome-assembled genomes from 7 cave sediment metagenomes. Assemblies’ taxonomy spanned 19 bacterial and three archaeal phyla with Acidobacteriota, Chloroflexota, Proteobacteria, Planctomycetota, Ca. Patescibacteria, Thermoproteota, Methylomirabilota, and Ca. Zixibacteria as prevalent phyla. Functional gene analyses predicted the presence of CO(2) fixation, methanotrophy, sulfur and ammonia oxidation in the explored sediments. Species Metabolic Coupling Analysis of metagenome-scale metabolic models revealed the highest competition-cooperation interactions in the sediments collected away from the water. Simulated metabolic interactions indicated autotrophs and methanotrophs as major donors of metabolites in the sediment communities. Cross-feeding dependencies were assumed only towards 'currency' molecules and inorganic compounds (O(2), PO(4)(3−), H(+), Fe(2+), Cu(2+)) in the water proximity sediment, whereas hydrogen sulfide and methanol were assumedly traded exclusively among distant gallery communities. CONCLUSIONS: These findings suggest that the primary production potential of Movile Cave expands way beyond its hydrothermal waters, enhancing our understanding of the functioning and ecological interactions within chemolithoautotrophically-based subterranean ecosystems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40793-022-00438-w. |
format | Online Article Text |
id | pubmed-9386943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93869432022-08-19 Competition-cooperation in the chemoautotrophic ecosystem of Movile Cave: first metagenomic approach on sediments Chiciudean, Iulia Russo, Giancarlo Bogdan, Diana Felicia Levei, Erika Andrea Faur, Luchiana Hillebrand-Voiculescu, Alexandra Moldovan, Oana Teodora Banciu, Horia Leonard Environ Microbiome Research BACKGROUND: Movile Cave (SE Romania) is a chemoautotrophically-based ecosystem fed by hydrogen sulfide-rich groundwater serving as a primary energy source analogous to the deep-sea hydrothermal ecosystems. Our current understanding of Movile Cave microbiology has been confined to the sulfidic water and its proximity, as most studies focused on the water-floating microbial mat and planktonic accumulations likely acting as the primary production powerhouse of this unique subterranean ecosystem. By employing comprehensive genomic-resolved metagenomics, we questioned the spatial variation, chemoautotrophic abilities, ecological interactions and trophic roles of Movile Cave’s microbiome thriving beyond the sulfidic-rich water. RESULTS: A customized bioinformatics pipeline led to the recovery of 106 high-quality metagenome-assembled genomes from 7 cave sediment metagenomes. Assemblies’ taxonomy spanned 19 bacterial and three archaeal phyla with Acidobacteriota, Chloroflexota, Proteobacteria, Planctomycetota, Ca. Patescibacteria, Thermoproteota, Methylomirabilota, and Ca. Zixibacteria as prevalent phyla. Functional gene analyses predicted the presence of CO(2) fixation, methanotrophy, sulfur and ammonia oxidation in the explored sediments. Species Metabolic Coupling Analysis of metagenome-scale metabolic models revealed the highest competition-cooperation interactions in the sediments collected away from the water. Simulated metabolic interactions indicated autotrophs and methanotrophs as major donors of metabolites in the sediment communities. Cross-feeding dependencies were assumed only towards 'currency' molecules and inorganic compounds (O(2), PO(4)(3−), H(+), Fe(2+), Cu(2+)) in the water proximity sediment, whereas hydrogen sulfide and methanol were assumedly traded exclusively among distant gallery communities. CONCLUSIONS: These findings suggest that the primary production potential of Movile Cave expands way beyond its hydrothermal waters, enhancing our understanding of the functioning and ecological interactions within chemolithoautotrophically-based subterranean ecosystems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40793-022-00438-w. BioMed Central 2022-08-17 /pmc/articles/PMC9386943/ /pubmed/35978381 http://dx.doi.org/10.1186/s40793-022-00438-w Text en © The Author(s) 2022 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 Chiciudean, Iulia Russo, Giancarlo Bogdan, Diana Felicia Levei, Erika Andrea Faur, Luchiana Hillebrand-Voiculescu, Alexandra Moldovan, Oana Teodora Banciu, Horia Leonard Competition-cooperation in the chemoautotrophic ecosystem of Movile Cave: first metagenomic approach on sediments |
title | Competition-cooperation in the chemoautotrophic ecosystem of Movile Cave: first metagenomic approach on sediments |
title_full | Competition-cooperation in the chemoautotrophic ecosystem of Movile Cave: first metagenomic approach on sediments |
title_fullStr | Competition-cooperation in the chemoautotrophic ecosystem of Movile Cave: first metagenomic approach on sediments |
title_full_unstemmed | Competition-cooperation in the chemoautotrophic ecosystem of Movile Cave: first metagenomic approach on sediments |
title_short | Competition-cooperation in the chemoautotrophic ecosystem of Movile Cave: first metagenomic approach on sediments |
title_sort | competition-cooperation in the chemoautotrophic ecosystem of movile cave: first metagenomic approach on sediments |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386943/ https://www.ncbi.nlm.nih.gov/pubmed/35978381 http://dx.doi.org/10.1186/s40793-022-00438-w |
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