Genome-Resolved Metagenomic Analysis Reveals Roles for Candidate Phyla and Other Microbial Community Members in Biogeochemical Transformations in Oil Reservoirs

ABSTRACT Oil reservoirs are major sites of methane production and carbon turnover, processes with significant impacts on energy resources and global biogeochemical cycles. We applied a cultivation-independent genomic approach to define microbial community membership and predict roles for specific or...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Ping Hu, Lauren Tom, Andrea Singh, Brian C. Thomas, Brett J. Baker, Yvette M. Piceno, Gary L. Andersen, Jillian F. Banfield
Formato: article
Lenguaje:EN
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://doaj.org/article/f6a7f457a0044edd872aa46355d3bf1c
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:f6a7f457a0044edd872aa46355d3bf1c
record_format dspace
spelling oai:doaj.org-article:f6a7f457a0044edd872aa46355d3bf1c2021-11-15T15:49:40ZGenome-Resolved Metagenomic Analysis Reveals Roles for Candidate Phyla and Other Microbial Community Members in Biogeochemical Transformations in Oil Reservoirs10.1128/mBio.01669-152150-7511https://doaj.org/article/f6a7f457a0044edd872aa46355d3bf1c2016-03-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01669-15https://doaj.org/toc/2150-7511ABSTRACT Oil reservoirs are major sites of methane production and carbon turnover, processes with significant impacts on energy resources and global biogeochemical cycles. We applied a cultivation-independent genomic approach to define microbial community membership and predict roles for specific organisms in biogeochemical transformations in Alaska North Slope oil fields. Produced water samples were collected from six locations between 1,128 m (24 to 27°C) and 2,743 m (80 to 83°C) below the surface. Microbial community complexity decreased with increasing temperature, and the potential to degrade hydrocarbon compounds was most prevalent in the lower-temperature reservoirs. Sulfate availability, rather than sulfate reduction potential, seems to be the limiting factor for sulfide production in some of the reservoirs under investigation. Most microorganisms in the intermediate- and higher-temperature samples were related to previously studied methanogenic and nonmethanogenic archaea and thermophilic bacteria, but one candidate phylum bacterium, a member of the Acetothermia (OP1), was present in Kuparuk sample K3. The greatest numbers of candidate phyla were recovered from the mesothermic reservoir samples SB1 and SB2. We reconstructed a nearly complete genome for an organism from the candidate phylum Parcubacteria (OD1) that was abundant in sample SB1. Consistent with prior findings for members of this lineage, the OD1 genome is small, and metabolic predictions support an obligately anaerobic, fermentation-based lifestyle. At moderate abundance in samples SB1 and SB2 were members of bacteria from other candidate phyla, including Microgenomates (OP11), Atribacteria (OP9), candidate phyla TA06 and WS6, and Marinimicrobia (SAR406). The results presented here elucidate potential roles of organisms in oil reservoir biological processes. IMPORTANCE The activities of microorganisms in oil reservoirs impact petroleum resource quality and the global carbon cycle. We show that bacteria belonging to candidate phyla are present in some oil reservoirs and provide the first insights into their potential roles in biogeochemical processes based on several nearly complete genomes.Ping HuLauren TomAndrea SinghBrian C. ThomasBrett J. BakerYvette M. PicenoGary L. AndersenJillian F. BanfieldAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 7, Iss 1 (2016)
institution DOAJ
collection DOAJ
language EN
topic Microbiology
QR1-502
spellingShingle Microbiology
QR1-502
Ping Hu
Lauren Tom
Andrea Singh
Brian C. Thomas
Brett J. Baker
Yvette M. Piceno
Gary L. Andersen
Jillian F. Banfield
Genome-Resolved Metagenomic Analysis Reveals Roles for Candidate Phyla and Other Microbial Community Members in Biogeochemical Transformations in Oil Reservoirs
description ABSTRACT Oil reservoirs are major sites of methane production and carbon turnover, processes with significant impacts on energy resources and global biogeochemical cycles. We applied a cultivation-independent genomic approach to define microbial community membership and predict roles for specific organisms in biogeochemical transformations in Alaska North Slope oil fields. Produced water samples were collected from six locations between 1,128 m (24 to 27°C) and 2,743 m (80 to 83°C) below the surface. Microbial community complexity decreased with increasing temperature, and the potential to degrade hydrocarbon compounds was most prevalent in the lower-temperature reservoirs. Sulfate availability, rather than sulfate reduction potential, seems to be the limiting factor for sulfide production in some of the reservoirs under investigation. Most microorganisms in the intermediate- and higher-temperature samples were related to previously studied methanogenic and nonmethanogenic archaea and thermophilic bacteria, but one candidate phylum bacterium, a member of the Acetothermia (OP1), was present in Kuparuk sample K3. The greatest numbers of candidate phyla were recovered from the mesothermic reservoir samples SB1 and SB2. We reconstructed a nearly complete genome for an organism from the candidate phylum Parcubacteria (OD1) that was abundant in sample SB1. Consistent with prior findings for members of this lineage, the OD1 genome is small, and metabolic predictions support an obligately anaerobic, fermentation-based lifestyle. At moderate abundance in samples SB1 and SB2 were members of bacteria from other candidate phyla, including Microgenomates (OP11), Atribacteria (OP9), candidate phyla TA06 and WS6, and Marinimicrobia (SAR406). The results presented here elucidate potential roles of organisms in oil reservoir biological processes. IMPORTANCE The activities of microorganisms in oil reservoirs impact petroleum resource quality and the global carbon cycle. We show that bacteria belonging to candidate phyla are present in some oil reservoirs and provide the first insights into their potential roles in biogeochemical processes based on several nearly complete genomes.
format article
author Ping Hu
Lauren Tom
Andrea Singh
Brian C. Thomas
Brett J. Baker
Yvette M. Piceno
Gary L. Andersen
Jillian F. Banfield
author_facet Ping Hu
Lauren Tom
Andrea Singh
Brian C. Thomas
Brett J. Baker
Yvette M. Piceno
Gary L. Andersen
Jillian F. Banfield
author_sort Ping Hu
title Genome-Resolved Metagenomic Analysis Reveals Roles for Candidate Phyla and Other Microbial Community Members in Biogeochemical Transformations in Oil Reservoirs
title_short Genome-Resolved Metagenomic Analysis Reveals Roles for Candidate Phyla and Other Microbial Community Members in Biogeochemical Transformations in Oil Reservoirs
title_full Genome-Resolved Metagenomic Analysis Reveals Roles for Candidate Phyla and Other Microbial Community Members in Biogeochemical Transformations in Oil Reservoirs
title_fullStr Genome-Resolved Metagenomic Analysis Reveals Roles for Candidate Phyla and Other Microbial Community Members in Biogeochemical Transformations in Oil Reservoirs
title_full_unstemmed Genome-Resolved Metagenomic Analysis Reveals Roles for Candidate Phyla and Other Microbial Community Members in Biogeochemical Transformations in Oil Reservoirs
title_sort genome-resolved metagenomic analysis reveals roles for candidate phyla and other microbial community members in biogeochemical transformations in oil reservoirs
publisher American Society for Microbiology
publishDate 2016
url https://doaj.org/article/f6a7f457a0044edd872aa46355d3bf1c
work_keys_str_mv AT pinghu genomeresolvedmetagenomicanalysisrevealsrolesforcandidatephylaandothermicrobialcommunitymembersinbiogeochemicaltransformationsinoilreservoirs
AT laurentom genomeresolvedmetagenomicanalysisrevealsrolesforcandidatephylaandothermicrobialcommunitymembersinbiogeochemicaltransformationsinoilreservoirs
AT andreasingh genomeresolvedmetagenomicanalysisrevealsrolesforcandidatephylaandothermicrobialcommunitymembersinbiogeochemicaltransformationsinoilreservoirs
AT briancthomas genomeresolvedmetagenomicanalysisrevealsrolesforcandidatephylaandothermicrobialcommunitymembersinbiogeochemicaltransformationsinoilreservoirs
AT brettjbaker genomeresolvedmetagenomicanalysisrevealsrolesforcandidatephylaandothermicrobialcommunitymembersinbiogeochemicaltransformationsinoilreservoirs
AT yvettempiceno genomeresolvedmetagenomicanalysisrevealsrolesforcandidatephylaandothermicrobialcommunitymembersinbiogeochemicaltransformationsinoilreservoirs
AT garylandersen genomeresolvedmetagenomicanalysisrevealsrolesforcandidatephylaandothermicrobialcommunitymembersinbiogeochemicaltransformationsinoilreservoirs
AT jillianfbanfield genomeresolvedmetagenomicanalysisrevealsrolesforcandidatephylaandothermicrobialcommunitymembersinbiogeochemicaltransformationsinoilreservoirs
_version_ 1718427497954017280