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Metagenomic Analysis Suggests Modern Freshwater Microbialites Harbor a Distinct Core Microbial Community

Modern microbialites are complex microbial communities that interface with abiotic factors to form carbonate-rich organosedimentary structures whose ancestors provide the earliest evidence of life. Past studies primarily on marine microbialites have inventoried diverse taxa and metabolic pathways, b...

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Autores principales: White, Richard Allen, Chan, Amy M., Gavelis, Gregory S., Leander, Brian S., Brady, Allyson L., Slater, Gregory F., Lim, Darlene S. S., Suttle, Curtis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729913/
https://www.ncbi.nlm.nih.gov/pubmed/26903951
http://dx.doi.org/10.3389/fmicb.2015.01531
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author White, Richard Allen
Chan, Amy M.
Gavelis, Gregory S.
Leander, Brian S.
Brady, Allyson L.
Slater, Gregory F.
Lim, Darlene S. S.
Suttle, Curtis A.
author_facet White, Richard Allen
Chan, Amy M.
Gavelis, Gregory S.
Leander, Brian S.
Brady, Allyson L.
Slater, Gregory F.
Lim, Darlene S. S.
Suttle, Curtis A.
author_sort White, Richard Allen
collection PubMed
description Modern microbialites are complex microbial communities that interface with abiotic factors to form carbonate-rich organosedimentary structures whose ancestors provide the earliest evidence of life. Past studies primarily on marine microbialites have inventoried diverse taxa and metabolic pathways, but it is unclear which of these are members of the microbialite community and which are introduced from adjacent environments. Here we control for these factors by sampling the surrounding water and nearby sediment, in addition to the microbialites and use a metagenomics approach to interrogate the microbial community. Our findings suggest that the Pavilion Lake microbialite community profile, metabolic potential and pathway distributions are distinct from those in the neighboring sediments and water. Based on RefSeq classification, members of the Proteobacteria (e.g., alpha and delta classes) were the dominant taxa in the microbialites, and possessed novel functional guilds associated with the metabolism of heavy metals, antibiotic resistance, primary alcohol biosynthesis and urea metabolism; the latter may help drive biomineralization. Urea metabolism within Pavilion Lake microbialites is a feature not previously associated in other microbialites. The microbialite communities were also significantly enriched for cyanobacteria and acidobacteria, which likely play an important role in biomineralization. Additional findings suggest that Pavilion Lake microbialites are under viral selection as genes associated with viral infection (e.g CRISPR-Cas, phage shock and phage excision) are abundant within the microbialite metagenomes. The morphology of Pavilion Lake microbialites changes dramatically with depth; yet, metagenomic data did not vary significantly by morphology or depth, indicating that microbialite morphology is altered by other factors, perhaps transcriptional differences or abiotic conditions. This work provides a comprehensive metagenomic perspective of the interactions and differences between microbialites and their surrounding environment, and reveals the distinct nature of these complex communities.
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spelling pubmed-47299132016-02-22 Metagenomic Analysis Suggests Modern Freshwater Microbialites Harbor a Distinct Core Microbial Community White, Richard Allen Chan, Amy M. Gavelis, Gregory S. Leander, Brian S. Brady, Allyson L. Slater, Gregory F. Lim, Darlene S. S. Suttle, Curtis A. Front Microbiol Microbiology Modern microbialites are complex microbial communities that interface with abiotic factors to form carbonate-rich organosedimentary structures whose ancestors provide the earliest evidence of life. Past studies primarily on marine microbialites have inventoried diverse taxa and metabolic pathways, but it is unclear which of these are members of the microbialite community and which are introduced from adjacent environments. Here we control for these factors by sampling the surrounding water and nearby sediment, in addition to the microbialites and use a metagenomics approach to interrogate the microbial community. Our findings suggest that the Pavilion Lake microbialite community profile, metabolic potential and pathway distributions are distinct from those in the neighboring sediments and water. Based on RefSeq classification, members of the Proteobacteria (e.g., alpha and delta classes) were the dominant taxa in the microbialites, and possessed novel functional guilds associated with the metabolism of heavy metals, antibiotic resistance, primary alcohol biosynthesis and urea metabolism; the latter may help drive biomineralization. Urea metabolism within Pavilion Lake microbialites is a feature not previously associated in other microbialites. The microbialite communities were also significantly enriched for cyanobacteria and acidobacteria, which likely play an important role in biomineralization. Additional findings suggest that Pavilion Lake microbialites are under viral selection as genes associated with viral infection (e.g CRISPR-Cas, phage shock and phage excision) are abundant within the microbialite metagenomes. The morphology of Pavilion Lake microbialites changes dramatically with depth; yet, metagenomic data did not vary significantly by morphology or depth, indicating that microbialite morphology is altered by other factors, perhaps transcriptional differences or abiotic conditions. This work provides a comprehensive metagenomic perspective of the interactions and differences between microbialites and their surrounding environment, and reveals the distinct nature of these complex communities. Frontiers Media S.A. 2016-01-28 /pmc/articles/PMC4729913/ /pubmed/26903951 http://dx.doi.org/10.3389/fmicb.2015.01531 Text en Copyright © 2016 White, Chan, Gavelis, Leander, Brady, Slater, Lim and Suttle. 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
White, Richard Allen
Chan, Amy M.
Gavelis, Gregory S.
Leander, Brian S.
Brady, Allyson L.
Slater, Gregory F.
Lim, Darlene S. S.
Suttle, Curtis A.
Metagenomic Analysis Suggests Modern Freshwater Microbialites Harbor a Distinct Core Microbial Community
title Metagenomic Analysis Suggests Modern Freshwater Microbialites Harbor a Distinct Core Microbial Community
title_full Metagenomic Analysis Suggests Modern Freshwater Microbialites Harbor a Distinct Core Microbial Community
title_fullStr Metagenomic Analysis Suggests Modern Freshwater Microbialites Harbor a Distinct Core Microbial Community
title_full_unstemmed Metagenomic Analysis Suggests Modern Freshwater Microbialites Harbor a Distinct Core Microbial Community
title_short Metagenomic Analysis Suggests Modern Freshwater Microbialites Harbor a Distinct Core Microbial Community
title_sort metagenomic analysis suggests modern freshwater microbialites harbor a distinct core microbial community
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729913/
https://www.ncbi.nlm.nih.gov/pubmed/26903951
http://dx.doi.org/10.3389/fmicb.2015.01531
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