Cargando…

Metapangenomic investigation provides insight into niche differentiation of methanogenic populations from the subsurface serpentinizing environment, Samail Ophiolite, Oman

Serpentinization reactions produce highly reduced waters that have hyperalkaline pH and that can have high concentrations of H(2) and CH(4). Putatively autotrophic methanogenic archaea have been identified in the subsurface waters of the Samail Ophiolite, Sultanate of Oman, though the strategies to...

Descripción completa

Detalles Bibliográficos
Autores principales: Thieringer, Patrick H., Boyd, Eric S., Templeton, Alexis S., Spear, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350532/
https://www.ncbi.nlm.nih.gov/pubmed/37465028
http://dx.doi.org/10.3389/fmicb.2023.1205558
_version_ 1785074154100228096
author Thieringer, Patrick H.
Boyd, Eric S.
Templeton, Alexis S.
Spear, John R.
author_facet Thieringer, Patrick H.
Boyd, Eric S.
Templeton, Alexis S.
Spear, John R.
author_sort Thieringer, Patrick H.
collection PubMed
description Serpentinization reactions produce highly reduced waters that have hyperalkaline pH and that can have high concentrations of H(2) and CH(4). Putatively autotrophic methanogenic archaea have been identified in the subsurface waters of the Samail Ophiolite, Sultanate of Oman, though the strategies to overcome hyperalkaline pH and dissolved inorganic carbon limitation remain to be fully understood. Here, we recovered metagenome assembled genomes (MAGs) and applied a metapangenomic approach to three different Methanobacterium populations to assess habitat-specific functional gene distribution. A Type I population was identified in the fluids with neutral pH, while a Type II and “Mixed” population were identified in the most hyperalkaline fluids (pH 11.63). The core genome of all Methanobacterium populations highlighted potential DNA scavenging techniques to overcome phosphate or nitrogen limitation induced by environmental conditions. With particular emphasis on the Mixed and Type II population found in the most hyperalkaline fluids, the accessory genomes unique to each population reflected adaptation mechanisms suggesting lifestyles that minimize niche overlap. In addition to previously reported metabolic capability to utilize formate as an electron donor and generate intracellular CO(2), the Type II population possessed genes relevant to defense against antimicrobials and assimilating potential osmoprotectants to provide cellular stability. The accessory genome of the Mixed population was enriched in genes for multiple glycosyltransferases suggesting reduced energetic costs by adhering to mineral surfaces or to other microorganisms, and fostering a non-motile lifestyle. These results highlight the niche differentiation of distinct Methanobacterium populations to circumvent the challenges of serpentinization impacted fluids through coexistence strategies, supporting our ability to understand controls on methanogenic lifestyles and adaptations within the serpentinizing subsurface fluids of the Samail Ophiolite.
format Online
Article
Text
id pubmed-10350532
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-103505322023-07-18 Metapangenomic investigation provides insight into niche differentiation of methanogenic populations from the subsurface serpentinizing environment, Samail Ophiolite, Oman Thieringer, Patrick H. Boyd, Eric S. Templeton, Alexis S. Spear, John R. Front Microbiol Microbiology Serpentinization reactions produce highly reduced waters that have hyperalkaline pH and that can have high concentrations of H(2) and CH(4). Putatively autotrophic methanogenic archaea have been identified in the subsurface waters of the Samail Ophiolite, Sultanate of Oman, though the strategies to overcome hyperalkaline pH and dissolved inorganic carbon limitation remain to be fully understood. Here, we recovered metagenome assembled genomes (MAGs) and applied a metapangenomic approach to three different Methanobacterium populations to assess habitat-specific functional gene distribution. A Type I population was identified in the fluids with neutral pH, while a Type II and “Mixed” population were identified in the most hyperalkaline fluids (pH 11.63). The core genome of all Methanobacterium populations highlighted potential DNA scavenging techniques to overcome phosphate or nitrogen limitation induced by environmental conditions. With particular emphasis on the Mixed and Type II population found in the most hyperalkaline fluids, the accessory genomes unique to each population reflected adaptation mechanisms suggesting lifestyles that minimize niche overlap. In addition to previously reported metabolic capability to utilize formate as an electron donor and generate intracellular CO(2), the Type II population possessed genes relevant to defense against antimicrobials and assimilating potential osmoprotectants to provide cellular stability. The accessory genome of the Mixed population was enriched in genes for multiple glycosyltransferases suggesting reduced energetic costs by adhering to mineral surfaces or to other microorganisms, and fostering a non-motile lifestyle. These results highlight the niche differentiation of distinct Methanobacterium populations to circumvent the challenges of serpentinization impacted fluids through coexistence strategies, supporting our ability to understand controls on methanogenic lifestyles and adaptations within the serpentinizing subsurface fluids of the Samail Ophiolite. Frontiers Media S.A. 2023-07-03 /pmc/articles/PMC10350532/ /pubmed/37465028 http://dx.doi.org/10.3389/fmicb.2023.1205558 Text en Copyright © 2023 Thieringer, Boyd, Templeton and Spear. https://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) and the copyright owner(s) 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
Thieringer, Patrick H.
Boyd, Eric S.
Templeton, Alexis S.
Spear, John R.
Metapangenomic investigation provides insight into niche differentiation of methanogenic populations from the subsurface serpentinizing environment, Samail Ophiolite, Oman
title Metapangenomic investigation provides insight into niche differentiation of methanogenic populations from the subsurface serpentinizing environment, Samail Ophiolite, Oman
title_full Metapangenomic investigation provides insight into niche differentiation of methanogenic populations from the subsurface serpentinizing environment, Samail Ophiolite, Oman
title_fullStr Metapangenomic investigation provides insight into niche differentiation of methanogenic populations from the subsurface serpentinizing environment, Samail Ophiolite, Oman
title_full_unstemmed Metapangenomic investigation provides insight into niche differentiation of methanogenic populations from the subsurface serpentinizing environment, Samail Ophiolite, Oman
title_short Metapangenomic investigation provides insight into niche differentiation of methanogenic populations from the subsurface serpentinizing environment, Samail Ophiolite, Oman
title_sort metapangenomic investigation provides insight into niche differentiation of methanogenic populations from the subsurface serpentinizing environment, samail ophiolite, oman
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350532/
https://www.ncbi.nlm.nih.gov/pubmed/37465028
http://dx.doi.org/10.3389/fmicb.2023.1205558
work_keys_str_mv AT thieringerpatrickh metapangenomicinvestigationprovidesinsightintonichedifferentiationofmethanogenicpopulationsfromthesubsurfaceserpentinizingenvironmentsamailophioliteoman
AT boyderics metapangenomicinvestigationprovidesinsightintonichedifferentiationofmethanogenicpopulationsfromthesubsurfaceserpentinizingenvironmentsamailophioliteoman
AT templetonalexiss metapangenomicinvestigationprovidesinsightintonichedifferentiationofmethanogenicpopulationsfromthesubsurfaceserpentinizingenvironmentsamailophioliteoman
AT spearjohnr metapangenomicinvestigationprovidesinsightintonichedifferentiationofmethanogenicpopulationsfromthesubsurfaceserpentinizingenvironmentsamailophioliteoman