Cargando…
Deep-Subsurface Pressure Stimulates Metabolic Plasticity in Shale-Colonizing Halanaerobium spp.
Bacterial Halanaerobium strains become the dominant persisting microbial community member in produced fluids across geographically distinct hydraulically fractured shales. Halanaerobium is believed to be inadvertently introduced into this environment during the drilling and fracturing process and mu...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544827/ https://www.ncbi.nlm.nih.gov/pubmed/30979840 http://dx.doi.org/10.1128/AEM.00018-19 |
_version_ | 1783423305809657856 |
---|---|
author | Booker, Anne E. Hoyt, David W. Meulia, Tea Eder, Elizabeth Nicora, Carrie D. Purvine, Samuel O. Daly, Rebecca A. Moore, Joseph D. Wunch, Kenneth Pfiffner, Susan M. Lipton, Mary S. Mouser, Paula J. Wrighton, Kelly C. Wilkins, Michael J. |
author_facet | Booker, Anne E. Hoyt, David W. Meulia, Tea Eder, Elizabeth Nicora, Carrie D. Purvine, Samuel O. Daly, Rebecca A. Moore, Joseph D. Wunch, Kenneth Pfiffner, Susan M. Lipton, Mary S. Mouser, Paula J. Wrighton, Kelly C. Wilkins, Michael J. |
author_sort | Booker, Anne E. |
collection | PubMed |
description | Bacterial Halanaerobium strains become the dominant persisting microbial community member in produced fluids across geographically distinct hydraulically fractured shales. Halanaerobium is believed to be inadvertently introduced into this environment during the drilling and fracturing process and must therefore tolerate large changes in pressure, temperature, and salinity. Here, we used a Halanaerobium strain isolated from a natural gas well in the Utica Point Pleasant formation to investigate metabolic and physiological responses to growth under high-pressure subsurface conditions. Laboratory incubations confirmed the ability of Halanaerobium congolense strain WG8 to grow under pressures representative of deep shale formations (21 to 48 MPa). Under these conditions, broad metabolic and physiological shifts were identified, including higher abundances of proteins associated with the production of extracellular polymeric substances. Confocal laser scanning microscopy indicated that extracellular polymeric substance (EPS) production was associated with greater cell aggregation when biomass was cultured at high pressure. Changes in Halanaerobium central carbon metabolism under the same conditions were inferred from nuclear magnetic resonance (NMR) and gas chromatography measurements, revealing large per-cell increases in production of ethanol, acetate, and propanol and cessation of hydrogen production. These metabolic shifts were associated with carbon flux through 1,2-propanediol in response to slower fluxes of carbon through stage 3 of glycolysis. Together, these results reveal the potential for bioclogging and corrosion (via organic acid fermentation products) associated with persistent Halanaerobium growth in deep, hydraulically fractured shale ecosystems, and offer new insights into cellular mechanisms that enable these strains to dominate deep-shale microbiomes. IMPORTANCE The hydraulic fracturing of deep-shale formations for hydrocarbon recovery accounts for approximately 60% of U.S. natural gas production. Microbial activity associated with this process is generally considered deleterious due to issues associated with sulfide production, microbially induced corrosion, and bioclogging in the subsurface. Here we demonstrate that a representative Halanaerobium species, frequently the dominant microbial taxon in hydraulically fractured shales, responds to pressures characteristic of the deep subsurface by shifting its metabolism to generate more corrosive organic acids and produce more polymeric substances that cause “clumping” of biomass. While the potential for increased corrosion of steel infrastructure and clogging of pores and fractures in the subsurface may significantly impact hydrocarbon recovery, these data also offer new insights for microbial control in these ecosystems. |
format | Online Article Text |
id | pubmed-6544827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-65448272019-06-24 Deep-Subsurface Pressure Stimulates Metabolic Plasticity in Shale-Colonizing Halanaerobium spp. Booker, Anne E. Hoyt, David W. Meulia, Tea Eder, Elizabeth Nicora, Carrie D. Purvine, Samuel O. Daly, Rebecca A. Moore, Joseph D. Wunch, Kenneth Pfiffner, Susan M. Lipton, Mary S. Mouser, Paula J. Wrighton, Kelly C. Wilkins, Michael J. Appl Environ Microbiol Environmental Microbiology Bacterial Halanaerobium strains become the dominant persisting microbial community member in produced fluids across geographically distinct hydraulically fractured shales. Halanaerobium is believed to be inadvertently introduced into this environment during the drilling and fracturing process and must therefore tolerate large changes in pressure, temperature, and salinity. Here, we used a Halanaerobium strain isolated from a natural gas well in the Utica Point Pleasant formation to investigate metabolic and physiological responses to growth under high-pressure subsurface conditions. Laboratory incubations confirmed the ability of Halanaerobium congolense strain WG8 to grow under pressures representative of deep shale formations (21 to 48 MPa). Under these conditions, broad metabolic and physiological shifts were identified, including higher abundances of proteins associated with the production of extracellular polymeric substances. Confocal laser scanning microscopy indicated that extracellular polymeric substance (EPS) production was associated with greater cell aggregation when biomass was cultured at high pressure. Changes in Halanaerobium central carbon metabolism under the same conditions were inferred from nuclear magnetic resonance (NMR) and gas chromatography measurements, revealing large per-cell increases in production of ethanol, acetate, and propanol and cessation of hydrogen production. These metabolic shifts were associated with carbon flux through 1,2-propanediol in response to slower fluxes of carbon through stage 3 of glycolysis. Together, these results reveal the potential for bioclogging and corrosion (via organic acid fermentation products) associated with persistent Halanaerobium growth in deep, hydraulically fractured shale ecosystems, and offer new insights into cellular mechanisms that enable these strains to dominate deep-shale microbiomes. IMPORTANCE The hydraulic fracturing of deep-shale formations for hydrocarbon recovery accounts for approximately 60% of U.S. natural gas production. Microbial activity associated with this process is generally considered deleterious due to issues associated with sulfide production, microbially induced corrosion, and bioclogging in the subsurface. Here we demonstrate that a representative Halanaerobium species, frequently the dominant microbial taxon in hydraulically fractured shales, responds to pressures characteristic of the deep subsurface by shifting its metabolism to generate more corrosive organic acids and produce more polymeric substances that cause “clumping” of biomass. While the potential for increased corrosion of steel infrastructure and clogging of pores and fractures in the subsurface may significantly impact hydrocarbon recovery, these data also offer new insights for microbial control in these ecosystems. American Society for Microbiology 2019-05-30 /pmc/articles/PMC6544827/ /pubmed/30979840 http://dx.doi.org/10.1128/AEM.00018-19 Text en Copyright © 2019 Booker et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Environmental Microbiology Booker, Anne E. Hoyt, David W. Meulia, Tea Eder, Elizabeth Nicora, Carrie D. Purvine, Samuel O. Daly, Rebecca A. Moore, Joseph D. Wunch, Kenneth Pfiffner, Susan M. Lipton, Mary S. Mouser, Paula J. Wrighton, Kelly C. Wilkins, Michael J. Deep-Subsurface Pressure Stimulates Metabolic Plasticity in Shale-Colonizing Halanaerobium spp. |
title | Deep-Subsurface Pressure Stimulates Metabolic Plasticity in Shale-Colonizing Halanaerobium spp. |
title_full | Deep-Subsurface Pressure Stimulates Metabolic Plasticity in Shale-Colonizing Halanaerobium spp. |
title_fullStr | Deep-Subsurface Pressure Stimulates Metabolic Plasticity in Shale-Colonizing Halanaerobium spp. |
title_full_unstemmed | Deep-Subsurface Pressure Stimulates Metabolic Plasticity in Shale-Colonizing Halanaerobium spp. |
title_short | Deep-Subsurface Pressure Stimulates Metabolic Plasticity in Shale-Colonizing Halanaerobium spp. |
title_sort | deep-subsurface pressure stimulates metabolic plasticity in shale-colonizing halanaerobium spp. |
topic | Environmental Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544827/ https://www.ncbi.nlm.nih.gov/pubmed/30979840 http://dx.doi.org/10.1128/AEM.00018-19 |
work_keys_str_mv | AT bookerannee deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT hoytdavidw deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT meuliatea deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT ederelizabeth deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT nicoracarried deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT purvinesamuelo deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT dalyrebeccaa deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT moorejosephd deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT wunchkenneth deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT pfiffnersusanm deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT liptonmarys deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT mouserpaulaj deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT wrightonkellyc deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp AT wilkinsmichaelj deepsubsurfacepressurestimulatesmetabolicplasticityinshalecolonizinghalanaerobiumspp |