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Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing

Large, sulfur-cycling, calcite-precipitating bacteria in the genus Achromatium represent a significant proportion of bacterial communities near sediment-water interfaces at sites throughout the world. Our understanding of their potentially crucial roles in calcium, carbon, sulfur, nitrogen, and iron...

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Autores principales: Mansor, Muammar, Hamilton, Trinity L., Fantle, Matthew S., 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/PMC4530308/
https://www.ncbi.nlm.nih.gov/pubmed/26322031
http://dx.doi.org/10.3389/fmicb.2015.00822
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author Mansor, Muammar
Hamilton, Trinity L.
Fantle, Matthew S.
Macalady, Jennifer L.
author_facet Mansor, Muammar
Hamilton, Trinity L.
Fantle, Matthew S.
Macalady, Jennifer L.
author_sort Mansor, Muammar
collection PubMed
description Large, sulfur-cycling, calcite-precipitating bacteria in the genus Achromatium represent a significant proportion of bacterial communities near sediment-water interfaces at sites throughout the world. Our understanding of their potentially crucial roles in calcium, carbon, sulfur, nitrogen, and iron cycling is limited because they have not been cultured or sequenced using environmental genomics approaches to date. We utilized single-cell genomic sequencing to obtain one incomplete and two nearly complete draft genomes for Achromatium collected at Warm Mineral Springs (WMS), FL. Based on 16S rRNA gene sequences, the three cells represent distinct and relatively distant Achromatium populations (91–92% identity). The draft genomes encode key genes involved in sulfur and hydrogen oxidation; oxygen, nitrogen and polysulfide respiration; carbon and nitrogen fixation; organic carbon assimilation and storage; chemotaxis; twitching motility; antibiotic resistance; and membrane transport. Known genes for iron and manganese energy metabolism were not detected. The presence of pyrophosphatase and vacuolar (V)-type ATPases, which are generally rare in bacterial genomes, suggests a role for these enzymes in calcium transport, proton pumping, and/or energy generation in the membranes of calcite-containing inclusions.
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spelling pubmed-45303082015-08-28 Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing Mansor, Muammar Hamilton, Trinity L. Fantle, Matthew S. Macalady, Jennifer L. Front Microbiol Microbiology Large, sulfur-cycling, calcite-precipitating bacteria in the genus Achromatium represent a significant proportion of bacterial communities near sediment-water interfaces at sites throughout the world. Our understanding of their potentially crucial roles in calcium, carbon, sulfur, nitrogen, and iron cycling is limited because they have not been cultured or sequenced using environmental genomics approaches to date. We utilized single-cell genomic sequencing to obtain one incomplete and two nearly complete draft genomes for Achromatium collected at Warm Mineral Springs (WMS), FL. Based on 16S rRNA gene sequences, the three cells represent distinct and relatively distant Achromatium populations (91–92% identity). The draft genomes encode key genes involved in sulfur and hydrogen oxidation; oxygen, nitrogen and polysulfide respiration; carbon and nitrogen fixation; organic carbon assimilation and storage; chemotaxis; twitching motility; antibiotic resistance; and membrane transport. Known genes for iron and manganese energy metabolism were not detected. The presence of pyrophosphatase and vacuolar (V)-type ATPases, which are generally rare in bacterial genomes, suggests a role for these enzymes in calcium transport, proton pumping, and/or energy generation in the membranes of calcite-containing inclusions. Frontiers Media S.A. 2015-08-10 /pmc/articles/PMC4530308/ /pubmed/26322031 http://dx.doi.org/10.3389/fmicb.2015.00822 Text en Copyright © 2015 Mansor, Hamilton, Fantle 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
Mansor, Muammar
Hamilton, Trinity L.
Fantle, Matthew S.
Macalady, Jennifer L.
Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing
title Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing
title_full Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing
title_fullStr Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing
title_full_unstemmed Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing
title_short Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing
title_sort metabolic diversity and ecological niches of achromatium populations revealed with single-cell genomic sequencing
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530308/
https://www.ncbi.nlm.nih.gov/pubmed/26322031
http://dx.doi.org/10.3389/fmicb.2015.00822
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