Cargando…

Metagenomic analysis and metabolite profiling of deep–sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill

Marine subsurface environments such as deep-sea sediments, house abundant and diverse microbial communities that are believed to influence large-scale geochemical processes. These processes include the biotransformation and mineralization of numerous petroleum constituents. Thus, microbial communiti...

Descripción completa

Detalles Bibliográficos
Autores principales: Kimes, Nikole E., Callaghan, Amy V., Aktas, Deniz F., Smith, Whitney L., Sunner, Jan, Golding, BernardT., Drozdowska, Marta, Hazen, Terry C., Suflita, Joseph M., Morris, Pamela J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598227/
https://www.ncbi.nlm.nih.gov/pubmed/23508965
http://dx.doi.org/10.3389/fmicb.2013.00050
_version_ 1782262742451748864
author Kimes, Nikole E.
Callaghan, Amy V.
Aktas, Deniz F.
Smith, Whitney L.
Sunner, Jan
Golding, BernardT.
Drozdowska, Marta
Hazen, Terry C.
Suflita, Joseph M.
Morris, Pamela J.
author_facet Kimes, Nikole E.
Callaghan, Amy V.
Aktas, Deniz F.
Smith, Whitney L.
Sunner, Jan
Golding, BernardT.
Drozdowska, Marta
Hazen, Terry C.
Suflita, Joseph M.
Morris, Pamela J.
author_sort Kimes, Nikole E.
collection PubMed
description Marine subsurface environments such as deep-sea sediments, house abundant and diverse microbial communities that are believed to influence large-scale geochemical processes. These processes include the biotransformation and mineralization of numerous petroleum constituents. Thus, microbial communities in the Gulf of Mexico are thought to be responsible for the intrinsic bioremediation of crude oil released by the Deepwater Horizon (DWH) oil spill. While hydrocarbon contamination is known to enrich for aerobic, oil-degrading bacteria in deep-seawater habitats, relatively little is known about the response of communities in deep-sea sediments, where low oxygen levels may hinder such a response. Here, we examined the hypothesis that increased hydrocarbon exposure results in an altered sediment microbial community structure that reflects the prospects for oil biodegradation under the prevailing conditions. We explore this hypothesis using metagenomic analysis and metabolite profiling of deep-sea sediment samples following the DWH oil spill. The presence of aerobic microbial communities and associated functional genes was consistent among all samples, whereas, a greater number of Deltaproteobacteria and anaerobic functional genes were found in sediments closest to the DWH blowout site. Metabolite profiling also revealed a greater number of putative metabolites in sediments surrounding the blowout zone relative to a background site located 127 km away. The mass spectral analysis of the putative metabolites revealed that alkylsuccinates remained below detection levels, but a homologous series of benzylsuccinates (with carbon chain lengths from 5 to 10) could be detected. Our findings suggest that increased exposure to hydrocarbons enriches for Deltaproteobacteria, which are known to be capable of anaerobic hydrocarbon metabolism. We also provide evidence for an active microbial community metabolizing aromatic hydrocarbons in deep-sea sediments of the Gulf of Mexico.
format Online
Article
Text
id pubmed-3598227
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-35982272013-03-18 Metagenomic analysis and metabolite profiling of deep–sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill Kimes, Nikole E. Callaghan, Amy V. Aktas, Deniz F. Smith, Whitney L. Sunner, Jan Golding, BernardT. Drozdowska, Marta Hazen, Terry C. Suflita, Joseph M. Morris, Pamela J. Front Microbiol Microbiology Marine subsurface environments such as deep-sea sediments, house abundant and diverse microbial communities that are believed to influence large-scale geochemical processes. These processes include the biotransformation and mineralization of numerous petroleum constituents. Thus, microbial communities in the Gulf of Mexico are thought to be responsible for the intrinsic bioremediation of crude oil released by the Deepwater Horizon (DWH) oil spill. While hydrocarbon contamination is known to enrich for aerobic, oil-degrading bacteria in deep-seawater habitats, relatively little is known about the response of communities in deep-sea sediments, where low oxygen levels may hinder such a response. Here, we examined the hypothesis that increased hydrocarbon exposure results in an altered sediment microbial community structure that reflects the prospects for oil biodegradation under the prevailing conditions. We explore this hypothesis using metagenomic analysis and metabolite profiling of deep-sea sediment samples following the DWH oil spill. The presence of aerobic microbial communities and associated functional genes was consistent among all samples, whereas, a greater number of Deltaproteobacteria and anaerobic functional genes were found in sediments closest to the DWH blowout site. Metabolite profiling also revealed a greater number of putative metabolites in sediments surrounding the blowout zone relative to a background site located 127 km away. The mass spectral analysis of the putative metabolites revealed that alkylsuccinates remained below detection levels, but a homologous series of benzylsuccinates (with carbon chain lengths from 5 to 10) could be detected. Our findings suggest that increased exposure to hydrocarbons enriches for Deltaproteobacteria, which are known to be capable of anaerobic hydrocarbon metabolism. We also provide evidence for an active microbial community metabolizing aromatic hydrocarbons in deep-sea sediments of the Gulf of Mexico. Frontiers Media S.A. 2013-03-15 /pmc/articles/PMC3598227/ /pubmed/23508965 http://dx.doi.org/10.3389/fmicb.2013.00050 Text en Copyright © Kimes, Callaghan, Aktas, Smith, Sunner, Golding, Drozdowska, Hazen, Suflita and Morris. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Microbiology
Kimes, Nikole E.
Callaghan, Amy V.
Aktas, Deniz F.
Smith, Whitney L.
Sunner, Jan
Golding, BernardT.
Drozdowska, Marta
Hazen, Terry C.
Suflita, Joseph M.
Morris, Pamela J.
Metagenomic analysis and metabolite profiling of deep–sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill
title Metagenomic analysis and metabolite profiling of deep–sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill
title_full Metagenomic analysis and metabolite profiling of deep–sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill
title_fullStr Metagenomic analysis and metabolite profiling of deep–sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill
title_full_unstemmed Metagenomic analysis and metabolite profiling of deep–sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill
title_short Metagenomic analysis and metabolite profiling of deep–sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill
title_sort metagenomic analysis and metabolite profiling of deep–sea sediments from the gulf of mexico following the deepwater horizon oil spill
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598227/
https://www.ncbi.nlm.nih.gov/pubmed/23508965
http://dx.doi.org/10.3389/fmicb.2013.00050
work_keys_str_mv AT kimesnikolee metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill
AT callaghanamyv metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill
AT aktasdenizf metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill
AT smithwhitneyl metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill
AT sunnerjan metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill
AT goldingbernardt metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill
AT drozdowskamarta metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill
AT hazenterryc metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill
AT suflitajosephm metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill
AT morrispamelaj metagenomicanalysisandmetaboliteprofilingofdeepseasedimentsfromthegulfofmexicofollowingthedeepwaterhorizonoilspill