The molecular phylogeny of Chionaster nivalis reveals a novel order of psychrophilic and globally distributed Tremellomycetes (Fungi, Basidiomycota)

Snow and ice present challenging substrates for cellular growth, yet microbial snow communities not only exist, but are diverse and ecologically impactful. These communities are dominated by green algae, but additional organisms, such as fungi, are also abundant and may be important for nutrient cyc...

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Published in:PLOS ONE
Main Authors: Irwin, Nicholas A. T., Twynstra, Chantelle S., Mathur, Varsha, Keeling, Patrick J.
Format: Text
Language:English
Published: Public Library of Science 2021
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Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990227/
http://www.ncbi.nlm.nih.gov/pubmed/33760841
https://doi.org/10.1371/journal.pone.0247594
id ftpubmed:oai:pubmedcentral.nih.gov:7990227
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spelling ftpubmed:oai:pubmedcentral.nih.gov:7990227 2023-05-15T15:09:57+02:00 The molecular phylogeny of Chionaster nivalis reveals a novel order of psychrophilic and globally distributed Tremellomycetes (Fungi, Basidiomycota) Irwin, Nicholas A. T. Twynstra, Chantelle S. Mathur, Varsha Keeling, Patrick J. 2021-03-24 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990227/ http://www.ncbi.nlm.nih.gov/pubmed/33760841 https://doi.org/10.1371/journal.pone.0247594 en eng Public Library of Science http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990227/ http://www.ncbi.nlm.nih.gov/pubmed/33760841 http://dx.doi.org/10.1371/journal.pone.0247594 © 2021 Irwin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. CC-BY PLoS One Research Article Text 2021 ftpubmed https://doi.org/10.1371/journal.pone.0247594 2021-04-11T00:22:46Z Snow and ice present challenging substrates for cellular growth, yet microbial snow communities not only exist, but are diverse and ecologically impactful. These communities are dominated by green algae, but additional organisms, such as fungi, are also abundant and may be important for nutrient cycling, syntrophic interactions, and community structure in general. However, little is known about these non-algal community members, including their taxonomic affiliations. An example of this is Chionaster nivalis, a unicellular fungus that is morphologically enigmatic and frequently observed in snow communities globally. Despite being described over one hundred years ago, the phylogeny and higher-level taxonomic classifications of C. nivalis remain unknown. Here, we isolated and sequenced the internal transcribed spacer (ITS) and the D1-D2 region of the large subunit ribosomal RNA gene of C. nivalis, providing a molecular barcode for future studies. Phylogenetic analyses using the ITS and D1-D2 region revealed that C. nivalis is part of a novel lineage in the class Tremellomycetes (Basidiomycota, Agaricomycotina) for which a new order Chionasterales ord. nov. (MB838717) and family Chionasteraceae fam. nov. (MB838718) are proposed. Comparisons between C. nivalis and sequences generated from environmental surveys revealed that the Chionasterales are globally distributed and probably psychrophilic, as they appear to be limited to the high alpine and arctic regions. These results highlight the unexplored diversity that exists within these extreme habitats and emphasize the utility of single-cell approaches in characterizing these complex algal-dominated communities. Text Arctic PubMed Central (PMC) Arctic PLOS ONE 16 3 e0247594
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Research Article
spellingShingle Research Article
Irwin, Nicholas A. T.
Twynstra, Chantelle S.
Mathur, Varsha
Keeling, Patrick J.
The molecular phylogeny of Chionaster nivalis reveals a novel order of psychrophilic and globally distributed Tremellomycetes (Fungi, Basidiomycota)
topic_facet Research Article
description Snow and ice present challenging substrates for cellular growth, yet microbial snow communities not only exist, but are diverse and ecologically impactful. These communities are dominated by green algae, but additional organisms, such as fungi, are also abundant and may be important for nutrient cycling, syntrophic interactions, and community structure in general. However, little is known about these non-algal community members, including their taxonomic affiliations. An example of this is Chionaster nivalis, a unicellular fungus that is morphologically enigmatic and frequently observed in snow communities globally. Despite being described over one hundred years ago, the phylogeny and higher-level taxonomic classifications of C. nivalis remain unknown. Here, we isolated and sequenced the internal transcribed spacer (ITS) and the D1-D2 region of the large subunit ribosomal RNA gene of C. nivalis, providing a molecular barcode for future studies. Phylogenetic analyses using the ITS and D1-D2 region revealed that C. nivalis is part of a novel lineage in the class Tremellomycetes (Basidiomycota, Agaricomycotina) for which a new order Chionasterales ord. nov. (MB838717) and family Chionasteraceae fam. nov. (MB838718) are proposed. Comparisons between C. nivalis and sequences generated from environmental surveys revealed that the Chionasterales are globally distributed and probably psychrophilic, as they appear to be limited to the high alpine and arctic regions. These results highlight the unexplored diversity that exists within these extreme habitats and emphasize the utility of single-cell approaches in characterizing these complex algal-dominated communities.
format Text
author Irwin, Nicholas A. T.
Twynstra, Chantelle S.
Mathur, Varsha
Keeling, Patrick J.
author_facet Irwin, Nicholas A. T.
Twynstra, Chantelle S.
Mathur, Varsha
Keeling, Patrick J.
author_sort Irwin, Nicholas A. T.
title The molecular phylogeny of Chionaster nivalis reveals a novel order of psychrophilic and globally distributed Tremellomycetes (Fungi, Basidiomycota)
title_short The molecular phylogeny of Chionaster nivalis reveals a novel order of psychrophilic and globally distributed Tremellomycetes (Fungi, Basidiomycota)
title_full The molecular phylogeny of Chionaster nivalis reveals a novel order of psychrophilic and globally distributed Tremellomycetes (Fungi, Basidiomycota)
title_fullStr The molecular phylogeny of Chionaster nivalis reveals a novel order of psychrophilic and globally distributed Tremellomycetes (Fungi, Basidiomycota)
title_full_unstemmed The molecular phylogeny of Chionaster nivalis reveals a novel order of psychrophilic and globally distributed Tremellomycetes (Fungi, Basidiomycota)
title_sort molecular phylogeny of chionaster nivalis reveals a novel order of psychrophilic and globally distributed tremellomycetes (fungi, basidiomycota)
publisher Public Library of Science
publishDate 2021
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990227/
http://www.ncbi.nlm.nih.gov/pubmed/33760841
https://doi.org/10.1371/journal.pone.0247594
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op_source PLoS One
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990227/
http://www.ncbi.nlm.nih.gov/pubmed/33760841
http://dx.doi.org/10.1371/journal.pone.0247594
op_rights © 2021 Irwin et al
http://creativecommons.org/licenses/by/4.0/
This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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