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Microbial succession during the transition from active to inactive stages of deep-sea hydrothermal vent sulfide chimneys

BACKGROUND: Deep-sea hydrothermal vents are highly productive biodiversity hotspots in the deep ocean supported by chemosynthetic microorganisms. Prominent features of these systems are sulfide chimneys emanating high-temperature hydrothermal fluids. While several studies have investigated the micro...

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Autores principales: Hou, Jialin, Sievert, Stefan M., Wang, Yinzhao, Seewald, Jeffrey S., Natarajan, Vengadesh Perumal, Wang, Fengping, Xiao, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329443/
https://www.ncbi.nlm.nih.gov/pubmed/32605604
http://dx.doi.org/10.1186/s40168-020-00851-8
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author Hou, Jialin
Sievert, Stefan M.
Wang, Yinzhao
Seewald, Jeffrey S.
Natarajan, Vengadesh Perumal
Wang, Fengping
Xiao, Xiang
author_facet Hou, Jialin
Sievert, Stefan M.
Wang, Yinzhao
Seewald, Jeffrey S.
Natarajan, Vengadesh Perumal
Wang, Fengping
Xiao, Xiang
author_sort Hou, Jialin
collection PubMed
description BACKGROUND: Deep-sea hydrothermal vents are highly productive biodiversity hotspots in the deep ocean supported by chemosynthetic microorganisms. Prominent features of these systems are sulfide chimneys emanating high-temperature hydrothermal fluids. While several studies have investigated the microbial diversity in both active and inactive sulfide chimneys that have been extinct for up to thousands of years, little is known about chimneys that have ceased activity more recently, as well as the microbial succession occurring during the transition from active to inactive chimneys. RESULTS: Genome-resolved metagenomics was applied to an active and a recently extinct (~ 7 years) sulfide chimney from the 9–10° N hydrothermal vent field on the East Pacific Rise. Full-length 16S rRNA gene and a total of 173 high-quality metagenome assembled genomes (MAGs) were retrieved for comparative analysis. In the active chimney (L-vent), sulfide- and/or hydrogen-oxidizing Campylobacteria and Aquificae with the potential for denitrification were identified as the dominant community members and primary producers, fixing carbon through the reductive tricarboxylic acid (rTCA) cycle. In contrast, the microbiome of the recently extinct chimney (M-vent) was largely composed of heterotrophs from various bacterial phyla, including Delta-/Beta-/Alphaproteobacteria and Bacteroidetes. Gammaproteobacteria were identified as the main primary producers, using the oxidation of metal sulfides and/or iron oxidation coupled to nitrate reduction to fix carbon through the Calvin-Benson-Bassham (CBB) cycle. Further analysis revealed a phylogenetically distinct Nitrospirae cluster that has the potential to oxidize sulfide minerals coupled to oxygen and/or nitrite reduction, as well as for sulfate reduction, and that might serve as an indicator for the early stages of chimneys after venting has ceased. CONCLUSIONS: This study sheds light on the composition, metabolic functions, and succession of microbial communities inhabiting deep-sea hydrothermal vent sulfide chimneys. Collectively, microbial succession during the life span of a chimney could be described to proceed from a “fluid-shaped” microbial community in newly formed and actively venting chimneys supported by the oxidation of reductants in the hydrothermal fluid to a “mineral-shaped” community supported by the oxidation of minerals after hydrothermal activity has ceased. Remarkably, the transition appears to occur within the first few years, after which the communities stay stable for thousands of years.
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spelling pubmed-73294432020-07-02 Microbial succession during the transition from active to inactive stages of deep-sea hydrothermal vent sulfide chimneys Hou, Jialin Sievert, Stefan M. Wang, Yinzhao Seewald, Jeffrey S. Natarajan, Vengadesh Perumal Wang, Fengping Xiao, Xiang Microbiome Research BACKGROUND: Deep-sea hydrothermal vents are highly productive biodiversity hotspots in the deep ocean supported by chemosynthetic microorganisms. Prominent features of these systems are sulfide chimneys emanating high-temperature hydrothermal fluids. While several studies have investigated the microbial diversity in both active and inactive sulfide chimneys that have been extinct for up to thousands of years, little is known about chimneys that have ceased activity more recently, as well as the microbial succession occurring during the transition from active to inactive chimneys. RESULTS: Genome-resolved metagenomics was applied to an active and a recently extinct (~ 7 years) sulfide chimney from the 9–10° N hydrothermal vent field on the East Pacific Rise. Full-length 16S rRNA gene and a total of 173 high-quality metagenome assembled genomes (MAGs) were retrieved for comparative analysis. In the active chimney (L-vent), sulfide- and/or hydrogen-oxidizing Campylobacteria and Aquificae with the potential for denitrification were identified as the dominant community members and primary producers, fixing carbon through the reductive tricarboxylic acid (rTCA) cycle. In contrast, the microbiome of the recently extinct chimney (M-vent) was largely composed of heterotrophs from various bacterial phyla, including Delta-/Beta-/Alphaproteobacteria and Bacteroidetes. Gammaproteobacteria were identified as the main primary producers, using the oxidation of metal sulfides and/or iron oxidation coupled to nitrate reduction to fix carbon through the Calvin-Benson-Bassham (CBB) cycle. Further analysis revealed a phylogenetically distinct Nitrospirae cluster that has the potential to oxidize sulfide minerals coupled to oxygen and/or nitrite reduction, as well as for sulfate reduction, and that might serve as an indicator for the early stages of chimneys after venting has ceased. CONCLUSIONS: This study sheds light on the composition, metabolic functions, and succession of microbial communities inhabiting deep-sea hydrothermal vent sulfide chimneys. Collectively, microbial succession during the life span of a chimney could be described to proceed from a “fluid-shaped” microbial community in newly formed and actively venting chimneys supported by the oxidation of reductants in the hydrothermal fluid to a “mineral-shaped” community supported by the oxidation of minerals after hydrothermal activity has ceased. Remarkably, the transition appears to occur within the first few years, after which the communities stay stable for thousands of years. BioMed Central 2020-06-30 /pmc/articles/PMC7329443/ /pubmed/32605604 http://dx.doi.org/10.1186/s40168-020-00851-8 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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
Hou, Jialin
Sievert, Stefan M.
Wang, Yinzhao
Seewald, Jeffrey S.
Natarajan, Vengadesh Perumal
Wang, Fengping
Xiao, Xiang
Microbial succession during the transition from active to inactive stages of deep-sea hydrothermal vent sulfide chimneys
title Microbial succession during the transition from active to inactive stages of deep-sea hydrothermal vent sulfide chimneys
title_full Microbial succession during the transition from active to inactive stages of deep-sea hydrothermal vent sulfide chimneys
title_fullStr Microbial succession during the transition from active to inactive stages of deep-sea hydrothermal vent sulfide chimneys
title_full_unstemmed Microbial succession during the transition from active to inactive stages of deep-sea hydrothermal vent sulfide chimneys
title_short Microbial succession during the transition from active to inactive stages of deep-sea hydrothermal vent sulfide chimneys
title_sort microbial succession during the transition from active to inactive stages of deep-sea hydrothermal vent sulfide chimneys
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329443/
https://www.ncbi.nlm.nih.gov/pubmed/32605604
http://dx.doi.org/10.1186/s40168-020-00851-8
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