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Ecophysiology and genomics of the brackish water adapted SAR11 subclade IIIa
The Order Pelagibacterales (SAR11) is the most abundant group of heterotrophic bacterioplankton in global oceans and comprises multiple subclades with unique spatiotemporal distributions. Subclade IIIa is the primary SAR11 group in brackish waters and shares a common ancestor with the dominant fresh...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030771/ https://www.ncbi.nlm.nih.gov/pubmed/36739346 http://dx.doi.org/10.1038/s41396-023-01376-2 |
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author | Lanclos, V. Celeste Rasmussen, Anna N. Kojima, Conner Y. Cheng, Chuankai Henson, Michael W. Faircloth, Brant C. Francis, Christopher A. Thrash, J. Cameron |
author_facet | Lanclos, V. Celeste Rasmussen, Anna N. Kojima, Conner Y. Cheng, Chuankai Henson, Michael W. Faircloth, Brant C. Francis, Christopher A. Thrash, J. Cameron |
author_sort | Lanclos, V. Celeste |
collection | PubMed |
description | The Order Pelagibacterales (SAR11) is the most abundant group of heterotrophic bacterioplankton in global oceans and comprises multiple subclades with unique spatiotemporal distributions. Subclade IIIa is the primary SAR11 group in brackish waters and shares a common ancestor with the dominant freshwater IIIb (LD12) subclade. Despite its dominance in brackish environments, subclade IIIa lacks systematic genomic or ecological studies. Here, we combine closed genomes from new IIIa isolates, new IIIa MAGS from San Francisco Bay (SFB), and 460 highly complete publicly available SAR11 genomes for the most comprehensive pangenomic study of subclade IIIa to date. Subclade IIIa represents a taxonomic family containing three genera (denoted as subgroups IIIa.1, IIIa.2, and IIIa.3) that had distinct ecological distributions related to salinity. The expansion of taxon selection within subclade IIIa also established previously noted metabolic differentiation in subclade IIIa compared to other SAR11 subclades such as glycine/serine prototrophy, mosaic glyoxylate shunt presence, and polyhydroxyalkanoate synthesis potential. Our analysis further shows metabolic flexibility among subgroups within IIIa. Additionally, we find that subclade IIIa.3 bridges the marine and freshwater clades based on its potential for compatible solute transport, iron utilization, and bicarbonate management potential. Pure culture experimentation validated differential salinity ranges in IIIa.1 and IIIa.3 and provided detailed IIIa cell size and volume data. This study is an important step forward for understanding the genomic, ecological, and physiological differentiation of subclade IIIa and the overall evolutionary history of SAR11. |
format | Online Article Text |
id | pubmed-10030771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100307712023-03-23 Ecophysiology and genomics of the brackish water adapted SAR11 subclade IIIa Lanclos, V. Celeste Rasmussen, Anna N. Kojima, Conner Y. Cheng, Chuankai Henson, Michael W. Faircloth, Brant C. Francis, Christopher A. Thrash, J. Cameron ISME J Article The Order Pelagibacterales (SAR11) is the most abundant group of heterotrophic bacterioplankton in global oceans and comprises multiple subclades with unique spatiotemporal distributions. Subclade IIIa is the primary SAR11 group in brackish waters and shares a common ancestor with the dominant freshwater IIIb (LD12) subclade. Despite its dominance in brackish environments, subclade IIIa lacks systematic genomic or ecological studies. Here, we combine closed genomes from new IIIa isolates, new IIIa MAGS from San Francisco Bay (SFB), and 460 highly complete publicly available SAR11 genomes for the most comprehensive pangenomic study of subclade IIIa to date. Subclade IIIa represents a taxonomic family containing three genera (denoted as subgroups IIIa.1, IIIa.2, and IIIa.3) that had distinct ecological distributions related to salinity. The expansion of taxon selection within subclade IIIa also established previously noted metabolic differentiation in subclade IIIa compared to other SAR11 subclades such as glycine/serine prototrophy, mosaic glyoxylate shunt presence, and polyhydroxyalkanoate synthesis potential. Our analysis further shows metabolic flexibility among subgroups within IIIa. Additionally, we find that subclade IIIa.3 bridges the marine and freshwater clades based on its potential for compatible solute transport, iron utilization, and bicarbonate management potential. Pure culture experimentation validated differential salinity ranges in IIIa.1 and IIIa.3 and provided detailed IIIa cell size and volume data. This study is an important step forward for understanding the genomic, ecological, and physiological differentiation of subclade IIIa and the overall evolutionary history of SAR11. Nature Publishing Group UK 2023-02-04 2023-04 /pmc/articles/PMC10030771/ /pubmed/36739346 http://dx.doi.org/10.1038/s41396-023-01376-2 Text en © The Author(s) 2023 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 Lanclos, V. Celeste Rasmussen, Anna N. Kojima, Conner Y. Cheng, Chuankai Henson, Michael W. Faircloth, Brant C. Francis, Christopher A. Thrash, J. Cameron Ecophysiology and genomics of the brackish water adapted SAR11 subclade IIIa |
title | Ecophysiology and genomics of the brackish water adapted SAR11 subclade IIIa |
title_full | Ecophysiology and genomics of the brackish water adapted SAR11 subclade IIIa |
title_fullStr | Ecophysiology and genomics of the brackish water adapted SAR11 subclade IIIa |
title_full_unstemmed | Ecophysiology and genomics of the brackish water adapted SAR11 subclade IIIa |
title_short | Ecophysiology and genomics of the brackish water adapted SAR11 subclade IIIa |
title_sort | ecophysiology and genomics of the brackish water adapted sar11 subclade iiia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030771/ https://www.ncbi.nlm.nih.gov/pubmed/36739346 http://dx.doi.org/10.1038/s41396-023-01376-2 |
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