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Insights into ecological roles of uncultivated bacteria in Katase hot spring sediment from long-read metagenomics
Diverse yet-uncultivated bacteria and archaea, i.e., microbial dark matter, are present in terrestrial hot spring environments. Numerous metagenome-assembled genomes (MAGs) of these uncultivated prokaryotes by short-read metagenomics have been reported so far, suggesting their metabolic potential. H...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671151/ https://www.ncbi.nlm.nih.gov/pubmed/36406403 http://dx.doi.org/10.3389/fmicb.2022.1045931 |
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author | Kato, Shingo Masuda, Sachiko Shibata, Arisa Shirasu, Ken Ohkuma, Moriya |
author_facet | Kato, Shingo Masuda, Sachiko Shibata, Arisa Shirasu, Ken Ohkuma, Moriya |
author_sort | Kato, Shingo |
collection | PubMed |
description | Diverse yet-uncultivated bacteria and archaea, i.e., microbial dark matter, are present in terrestrial hot spring environments. Numerous metagenome-assembled genomes (MAGs) of these uncultivated prokaryotes by short-read metagenomics have been reported so far, suggesting their metabolic potential. However, more reliable MAGs, i.e., circularized complete MAGs (cMAGs), have been rarely reported from hot spring environments. Here, we report 61 high-quality (HQ)-MAGs, including 14 cMAGs, of diverse uncultivated bacteria and archaea retrieved from hot spring sediment (52°C, pH 7.2) by highly accurate long-read sequencing using PacBio Sequel II. The HQ MAGs were affiliated with one archaeal and 13 bacterial phyla. Notably, nine of the 14 cMAGs were the first reported cMAGs for the family- to class-level clades that these cMAGs belonged to. The genome information suggests that the bacteria represented by MAGs play a significant role in the biogeochemical cycling of carbon, nitrogen, iron, and sulfur at this site. In particular, the genome analysis of six HQ MAGs including two cMAGs of Armatimonadota, of which members are frequently abundant in hot spring environments, predicts that they are aerobic, moderate thermophilic chemoorganoheterotrophs, and potentially oxidize and/or reduce iron. This prediction is consistent with the environmental conditions where they were detected. Our results expand the knowledge regarding the ecological potential of uncultivated bacteria in moderately-high-temperature environments. |
format | Online Article Text |
id | pubmed-9671151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96711512022-11-18 Insights into ecological roles of uncultivated bacteria in Katase hot spring sediment from long-read metagenomics Kato, Shingo Masuda, Sachiko Shibata, Arisa Shirasu, Ken Ohkuma, Moriya Front Microbiol Microbiology Diverse yet-uncultivated bacteria and archaea, i.e., microbial dark matter, are present in terrestrial hot spring environments. Numerous metagenome-assembled genomes (MAGs) of these uncultivated prokaryotes by short-read metagenomics have been reported so far, suggesting their metabolic potential. However, more reliable MAGs, i.e., circularized complete MAGs (cMAGs), have been rarely reported from hot spring environments. Here, we report 61 high-quality (HQ)-MAGs, including 14 cMAGs, of diverse uncultivated bacteria and archaea retrieved from hot spring sediment (52°C, pH 7.2) by highly accurate long-read sequencing using PacBio Sequel II. The HQ MAGs were affiliated with one archaeal and 13 bacterial phyla. Notably, nine of the 14 cMAGs were the first reported cMAGs for the family- to class-level clades that these cMAGs belonged to. The genome information suggests that the bacteria represented by MAGs play a significant role in the biogeochemical cycling of carbon, nitrogen, iron, and sulfur at this site. In particular, the genome analysis of six HQ MAGs including two cMAGs of Armatimonadota, of which members are frequently abundant in hot spring environments, predicts that they are aerobic, moderate thermophilic chemoorganoheterotrophs, and potentially oxidize and/or reduce iron. This prediction is consistent with the environmental conditions where they were detected. Our results expand the knowledge regarding the ecological potential of uncultivated bacteria in moderately-high-temperature environments. Frontiers Media S.A. 2022-11-03 /pmc/articles/PMC9671151/ /pubmed/36406403 http://dx.doi.org/10.3389/fmicb.2022.1045931 Text en Copyright © 2022 Kato, Masuda, Shibata, Shirasu and Ohkuma. 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 Kato, Shingo Masuda, Sachiko Shibata, Arisa Shirasu, Ken Ohkuma, Moriya Insights into ecological roles of uncultivated bacteria in Katase hot spring sediment from long-read metagenomics |
title | Insights into ecological roles of uncultivated bacteria in Katase hot spring sediment from long-read metagenomics |
title_full | Insights into ecological roles of uncultivated bacteria in Katase hot spring sediment from long-read metagenomics |
title_fullStr | Insights into ecological roles of uncultivated bacteria in Katase hot spring sediment from long-read metagenomics |
title_full_unstemmed | Insights into ecological roles of uncultivated bacteria in Katase hot spring sediment from long-read metagenomics |
title_short | Insights into ecological roles of uncultivated bacteria in Katase hot spring sediment from long-read metagenomics |
title_sort | insights into ecological roles of uncultivated bacteria in katase hot spring sediment from long-read metagenomics |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671151/ https://www.ncbi.nlm.nih.gov/pubmed/36406403 http://dx.doi.org/10.3389/fmicb.2022.1045931 |
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