Cargando…

Microbial colonization and persistence in deep fractured shales is guided by metabolic exchanges and viral predation

BACKGROUND: Microbial colonization of subsurface shales following hydraulic fracturing offers the opportunity to study coupled biotic and abiotic factors that impact microbial persistence in engineered deep subsurface ecosystems. Shale formations underly much of the continental USA and display geogr...

Descripción completa

Detalles Bibliográficos
Autores principales: Amundson, Kaela K., Borton, Mikayla A., Daly, Rebecca A., Hoyt, David W., Wong, Allison, Eder, Elizabeth, Moore, Joseph, Wunch, Kenneth, Wrighton, Kelly C., Wilkins, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762873/
https://www.ncbi.nlm.nih.gov/pubmed/35034639
http://dx.doi.org/10.1186/s40168-021-01194-8
_version_ 1784633836004442112
author Amundson, Kaela K.
Borton, Mikayla A.
Daly, Rebecca A.
Hoyt, David W.
Wong, Allison
Eder, Elizabeth
Moore, Joseph
Wunch, Kenneth
Wrighton, Kelly C.
Wilkins, Michael J.
author_facet Amundson, Kaela K.
Borton, Mikayla A.
Daly, Rebecca A.
Hoyt, David W.
Wong, Allison
Eder, Elizabeth
Moore, Joseph
Wunch, Kenneth
Wrighton, Kelly C.
Wilkins, Michael J.
author_sort Amundson, Kaela K.
collection PubMed
description BACKGROUND: Microbial colonization of subsurface shales following hydraulic fracturing offers the opportunity to study coupled biotic and abiotic factors that impact microbial persistence in engineered deep subsurface ecosystems. Shale formations underly much of the continental USA and display geographically distinct gradients in temperature and salinity. Complementing studies performed in eastern USA shales that contain brine-like fluids, here we coupled metagenomic and metabolomic approaches to develop the first genome-level insights into ecosystem colonization and microbial community interactions in a lower-salinity, but high-temperature western USA shale formation. RESULTS: We collected materials used during the hydraulic fracturing process (i.e., chemicals, drill muds) paired with temporal sampling of water produced from three different hydraulically fractured wells in the STACK (Sooner Trend Anadarko Basin, Canadian and Kingfisher) shale play in OK, USA. Relative to other shale formations, our metagenomic and metabolomic analyses revealed an expanded taxonomic and metabolic diversity of microorganisms that colonize and persist in fractured shales. Importantly, temporal sampling across all three hydraulic fracturing wells traced the degradation of complex polymers from the hydraulic fracturing process to the production and consumption of organic acids that support sulfate- and thiosulfate-reducing bacteria. Furthermore, we identified 5587 viral genomes and linked many of these to the dominant, colonizing microorganisms, demonstrating the key role that viral predation plays in community dynamics within this closed, engineered system. Lastly, top-side audit sampling of different source materials enabled genome-resolved source tracking, revealing the likely sources of many key colonizing and persisting taxa in these ecosystems. CONCLUSIONS: These findings highlight the importance of resource utilization and resistance to viral predation as key traits that enable specific microbial taxa to persist across fractured shale ecosystems. We also demonstrate the importance of materials used in the hydraulic fracturing process as both a source of persisting shale microorganisms and organic substrates that likely aid in sustaining the microbial community. Moreover, we showed that different physicochemical conditions (i.e., salinity, temperature) can influence the composition and functional potential of persisting microbial communities in shale ecosystems. Together, these results expand our knowledge of microbial life in deep subsurface shales and have important ramifications for management and treatment of microbial biomass in hydraulically fractured wells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01194-8.
format Online
Article
Text
id pubmed-8762873
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-87628732022-01-18 Microbial colonization and persistence in deep fractured shales is guided by metabolic exchanges and viral predation Amundson, Kaela K. Borton, Mikayla A. Daly, Rebecca A. Hoyt, David W. Wong, Allison Eder, Elizabeth Moore, Joseph Wunch, Kenneth Wrighton, Kelly C. Wilkins, Michael J. Microbiome Research BACKGROUND: Microbial colonization of subsurface shales following hydraulic fracturing offers the opportunity to study coupled biotic and abiotic factors that impact microbial persistence in engineered deep subsurface ecosystems. Shale formations underly much of the continental USA and display geographically distinct gradients in temperature and salinity. Complementing studies performed in eastern USA shales that contain brine-like fluids, here we coupled metagenomic and metabolomic approaches to develop the first genome-level insights into ecosystem colonization and microbial community interactions in a lower-salinity, but high-temperature western USA shale formation. RESULTS: We collected materials used during the hydraulic fracturing process (i.e., chemicals, drill muds) paired with temporal sampling of water produced from three different hydraulically fractured wells in the STACK (Sooner Trend Anadarko Basin, Canadian and Kingfisher) shale play in OK, USA. Relative to other shale formations, our metagenomic and metabolomic analyses revealed an expanded taxonomic and metabolic diversity of microorganisms that colonize and persist in fractured shales. Importantly, temporal sampling across all three hydraulic fracturing wells traced the degradation of complex polymers from the hydraulic fracturing process to the production and consumption of organic acids that support sulfate- and thiosulfate-reducing bacteria. Furthermore, we identified 5587 viral genomes and linked many of these to the dominant, colonizing microorganisms, demonstrating the key role that viral predation plays in community dynamics within this closed, engineered system. Lastly, top-side audit sampling of different source materials enabled genome-resolved source tracking, revealing the likely sources of many key colonizing and persisting taxa in these ecosystems. CONCLUSIONS: These findings highlight the importance of resource utilization and resistance to viral predation as key traits that enable specific microbial taxa to persist across fractured shale ecosystems. We also demonstrate the importance of materials used in the hydraulic fracturing process as both a source of persisting shale microorganisms and organic substrates that likely aid in sustaining the microbial community. Moreover, we showed that different physicochemical conditions (i.e., salinity, temperature) can influence the composition and functional potential of persisting microbial communities in shale ecosystems. Together, these results expand our knowledge of microbial life in deep subsurface shales and have important ramifications for management and treatment of microbial biomass in hydraulically fractured wells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01194-8. BioMed Central 2022-01-16 /pmc/articles/PMC8762873/ /pubmed/35034639 http://dx.doi.org/10.1186/s40168-021-01194-8 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Amundson, Kaela K.
Borton, Mikayla A.
Daly, Rebecca A.
Hoyt, David W.
Wong, Allison
Eder, Elizabeth
Moore, Joseph
Wunch, Kenneth
Wrighton, Kelly C.
Wilkins, Michael J.
Microbial colonization and persistence in deep fractured shales is guided by metabolic exchanges and viral predation
title Microbial colonization and persistence in deep fractured shales is guided by metabolic exchanges and viral predation
title_full Microbial colonization and persistence in deep fractured shales is guided by metabolic exchanges and viral predation
title_fullStr Microbial colonization and persistence in deep fractured shales is guided by metabolic exchanges and viral predation
title_full_unstemmed Microbial colonization and persistence in deep fractured shales is guided by metabolic exchanges and viral predation
title_short Microbial colonization and persistence in deep fractured shales is guided by metabolic exchanges and viral predation
title_sort microbial colonization and persistence in deep fractured shales is guided by metabolic exchanges and viral predation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762873/
https://www.ncbi.nlm.nih.gov/pubmed/35034639
http://dx.doi.org/10.1186/s40168-021-01194-8
work_keys_str_mv AT amundsonkaelak microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation
AT bortonmikaylaa microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation
AT dalyrebeccaa microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation
AT hoytdavidw microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation
AT wongallison microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation
AT ederelizabeth microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation
AT moorejoseph microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation
AT wunchkenneth microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation
AT wrightonkellyc microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation
AT wilkinsmichaelj microbialcolonizationandpersistenceindeepfracturedshalesisguidedbymetabolicexchangesandviralpredation