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Evolutionary stasis of a deep subsurface microbial lineage
Sulfate-reducing bacteria Candidatus Desulforudis audaxviator (CDA) were originally discovered in deep fracture fluids accessed via South African gold mines and have since been found in geographically widespread deep subsurface locations. In order to constrain models for subsurface microbial evoluti...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443664/ https://www.ncbi.nlm.nih.gov/pubmed/33824425 http://dx.doi.org/10.1038/s41396-021-00965-3 |
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author | Becraft, Eric D. Lau Vetter, Maggie C. Y. Bezuidt, Oliver K. I. Brown, Julia M. Labonté, Jessica M. Kauneckaite-Griguole, Kotryna Salkauskaite, Ruta Alzbutas, Gediminas Sackett, Joshua D. Kruger, Brittany R. Kadnikov, Vitaly van Heerden, Esta Moser, Duane Ravin, Nikolai Onstott, Tullis Stepanauskas, Ramunas |
author_facet | Becraft, Eric D. Lau Vetter, Maggie C. Y. Bezuidt, Oliver K. I. Brown, Julia M. Labonté, Jessica M. Kauneckaite-Griguole, Kotryna Salkauskaite, Ruta Alzbutas, Gediminas Sackett, Joshua D. Kruger, Brittany R. Kadnikov, Vitaly van Heerden, Esta Moser, Duane Ravin, Nikolai Onstott, Tullis Stepanauskas, Ramunas |
author_sort | Becraft, Eric D. |
collection | PubMed |
description | Sulfate-reducing bacteria Candidatus Desulforudis audaxviator (CDA) were originally discovered in deep fracture fluids accessed via South African gold mines and have since been found in geographically widespread deep subsurface locations. In order to constrain models for subsurface microbial evolution, we compared CDA genomes from Africa, North America and Eurasia using single cell genomics. Unexpectedly, 126 partial single amplified genomes from the three continents, a complete genome from of an isolate from Eurasia, and metagenome-assembled genomes from Africa and Eurasia shared >99.2% average nucleotide identity, low frequency of SNP’s, and near-perfectly conserved prophages and CRISPRs. Our analyses reject sample cross-contamination, recent natural dispersal, and unusually strong purifying selection as likely explanations for these unexpected results. We therefore conclude that the analyzed CDA populations underwent only minimal evolution since their physical separation, potentially as far back as the breakup of Pangea between 165 and 55 Ma ago. High-fidelity DNA replication and repair mechanisms are the most plausible explanation for the highly conserved genome of CDA. CDA presents a stark contrast to the current model organisms in microbial evolutionary studies, which often develop adaptive traits over far shorter periods of time. |
format | Online Article Text |
id | pubmed-8443664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84436642021-10-04 Evolutionary stasis of a deep subsurface microbial lineage Becraft, Eric D. Lau Vetter, Maggie C. Y. Bezuidt, Oliver K. I. Brown, Julia M. Labonté, Jessica M. Kauneckaite-Griguole, Kotryna Salkauskaite, Ruta Alzbutas, Gediminas Sackett, Joshua D. Kruger, Brittany R. Kadnikov, Vitaly van Heerden, Esta Moser, Duane Ravin, Nikolai Onstott, Tullis Stepanauskas, Ramunas ISME J Article Sulfate-reducing bacteria Candidatus Desulforudis audaxviator (CDA) were originally discovered in deep fracture fluids accessed via South African gold mines and have since been found in geographically widespread deep subsurface locations. In order to constrain models for subsurface microbial evolution, we compared CDA genomes from Africa, North America and Eurasia using single cell genomics. Unexpectedly, 126 partial single amplified genomes from the three continents, a complete genome from of an isolate from Eurasia, and metagenome-assembled genomes from Africa and Eurasia shared >99.2% average nucleotide identity, low frequency of SNP’s, and near-perfectly conserved prophages and CRISPRs. Our analyses reject sample cross-contamination, recent natural dispersal, and unusually strong purifying selection as likely explanations for these unexpected results. We therefore conclude that the analyzed CDA populations underwent only minimal evolution since their physical separation, potentially as far back as the breakup of Pangea between 165 and 55 Ma ago. High-fidelity DNA replication and repair mechanisms are the most plausible explanation for the highly conserved genome of CDA. CDA presents a stark contrast to the current model organisms in microbial evolutionary studies, which often develop adaptive traits over far shorter periods of time. Nature Publishing Group UK 2021-04-06 2021-10 /pmc/articles/PMC8443664/ /pubmed/33824425 http://dx.doi.org/10.1038/s41396-021-00965-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Becraft, Eric D. Lau Vetter, Maggie C. Y. Bezuidt, Oliver K. I. Brown, Julia M. Labonté, Jessica M. Kauneckaite-Griguole, Kotryna Salkauskaite, Ruta Alzbutas, Gediminas Sackett, Joshua D. Kruger, Brittany R. Kadnikov, Vitaly van Heerden, Esta Moser, Duane Ravin, Nikolai Onstott, Tullis Stepanauskas, Ramunas Evolutionary stasis of a deep subsurface microbial lineage |
title | Evolutionary stasis of a deep subsurface microbial lineage |
title_full | Evolutionary stasis of a deep subsurface microbial lineage |
title_fullStr | Evolutionary stasis of a deep subsurface microbial lineage |
title_full_unstemmed | Evolutionary stasis of a deep subsurface microbial lineage |
title_short | Evolutionary stasis of a deep subsurface microbial lineage |
title_sort | evolutionary stasis of a deep subsurface microbial lineage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443664/ https://www.ncbi.nlm.nih.gov/pubmed/33824425 http://dx.doi.org/10.1038/s41396-021-00965-3 |
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