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Metagenomic insights into S(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem

The Frasassi and Acquasanta Terme cave systems in Italy host isolated lithoautotrophic ecosystems characterized by sulfur-oxidizing biofilms with up to 50% S(0) by mass. The net contributions of microbial taxa in the biofilms to production and consumption of S(0) are poorly understood and have impli...

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Autores principales: Hamilton, Trinity L., Jones, Daniel S., Schaperdoth, Irene, Macalady, Jennifer L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288042/
https://www.ncbi.nlm.nih.gov/pubmed/25620962
http://dx.doi.org/10.3389/fmicb.2014.00756
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author Hamilton, Trinity L.
Jones, Daniel S.
Schaperdoth, Irene
Macalady, Jennifer L.
author_facet Hamilton, Trinity L.
Jones, Daniel S.
Schaperdoth, Irene
Macalady, Jennifer L.
author_sort Hamilton, Trinity L.
collection PubMed
description The Frasassi and Acquasanta Terme cave systems in Italy host isolated lithoautotrophic ecosystems characterized by sulfur-oxidizing biofilms with up to 50% S(0) by mass. The net contributions of microbial taxa in the biofilms to production and consumption of S(0) are poorly understood and have implications for understanding the formation of geological sulfur deposits as well as the ecological niches of sulfur-oxidizing autotrophs. Filamentous Epsilonproteobacteria are among the principal biofilm architects in Frasassi and Acquasanta Terme streams, colonizing high-sulfide, low-oxygen niches relative to other major biofilm-forming populations. Metagenomic sequencing of eight biofilm samples indicated the presence of diverse and abundant Epsilonproteobacteria. Populations of Sulfurovum-like organisms were the most abundant Epsilonproteobacteria regardless of differences in biofilm morphology, temperature, or water chemistry. After assembling and binning the metagenomic data, we retrieved four nearly-complete genomes of Sulfurovum-like organisms as well as a Sulfuricurvum spp. Analyses of the binned and assembled metagenomic data indicate that the Epsilonproteobacteria are autotrophic and therefore provide organic carbon to the isolated subsurface ecosystem. Multiple homologs of sulfide-quinone oxidoreductase (Sqr), together with incomplete or absent Sox pathways, suggest that cave Sulfurovum-like Epsilonproteobacteria oxidize sulfide incompletely to S(0) using either O(2) or nitrate as a terminal electron acceptor, consistent with previous evidence that they are most successful in niches with high dissolved sulfide to oxygen ratios. In contrast, we recovered homologs of the complete complement of Sox proteins affiliated Gammaproteobacteria and with less abundant Sulfuricurvum spp. and Arcobacter spp., suggesting that these populations are capable of the complete oxidation of sulfide to sulfate. These and other genomic data presented here offer new clues into the physiology and genetic potential of the largely uncultivated and ecologically successful cave Sulfurovum-like populations, and suggest that they play an integral role in subsurface S(0) formation.
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spelling pubmed-42880422015-01-23 Metagenomic insights into S(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem Hamilton, Trinity L. Jones, Daniel S. Schaperdoth, Irene Macalady, Jennifer L. Front Microbiol Microbiology The Frasassi and Acquasanta Terme cave systems in Italy host isolated lithoautotrophic ecosystems characterized by sulfur-oxidizing biofilms with up to 50% S(0) by mass. The net contributions of microbial taxa in the biofilms to production and consumption of S(0) are poorly understood and have implications for understanding the formation of geological sulfur deposits as well as the ecological niches of sulfur-oxidizing autotrophs. Filamentous Epsilonproteobacteria are among the principal biofilm architects in Frasassi and Acquasanta Terme streams, colonizing high-sulfide, low-oxygen niches relative to other major biofilm-forming populations. Metagenomic sequencing of eight biofilm samples indicated the presence of diverse and abundant Epsilonproteobacteria. Populations of Sulfurovum-like organisms were the most abundant Epsilonproteobacteria regardless of differences in biofilm morphology, temperature, or water chemistry. After assembling and binning the metagenomic data, we retrieved four nearly-complete genomes of Sulfurovum-like organisms as well as a Sulfuricurvum spp. Analyses of the binned and assembled metagenomic data indicate that the Epsilonproteobacteria are autotrophic and therefore provide organic carbon to the isolated subsurface ecosystem. Multiple homologs of sulfide-quinone oxidoreductase (Sqr), together with incomplete or absent Sox pathways, suggest that cave Sulfurovum-like Epsilonproteobacteria oxidize sulfide incompletely to S(0) using either O(2) or nitrate as a terminal electron acceptor, consistent with previous evidence that they are most successful in niches with high dissolved sulfide to oxygen ratios. In contrast, we recovered homologs of the complete complement of Sox proteins affiliated Gammaproteobacteria and with less abundant Sulfuricurvum spp. and Arcobacter spp., suggesting that these populations are capable of the complete oxidation of sulfide to sulfate. These and other genomic data presented here offer new clues into the physiology and genetic potential of the largely uncultivated and ecologically successful cave Sulfurovum-like populations, and suggest that they play an integral role in subsurface S(0) formation. Frontiers Media S.A. 2015-01-08 /pmc/articles/PMC4288042/ /pubmed/25620962 http://dx.doi.org/10.3389/fmicb.2014.00756 Text en Copyright © 2015 Hamilton, Jones, Schaperdoth and Macalady. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Hamilton, Trinity L.
Jones, Daniel S.
Schaperdoth, Irene
Macalady, Jennifer L.
Metagenomic insights into S(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem
title Metagenomic insights into S(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem
title_full Metagenomic insights into S(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem
title_fullStr Metagenomic insights into S(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem
title_full_unstemmed Metagenomic insights into S(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem
title_short Metagenomic insights into S(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem
title_sort metagenomic insights into s(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288042/
https://www.ncbi.nlm.nih.gov/pubmed/25620962
http://dx.doi.org/10.3389/fmicb.2014.00756
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