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Cyanolichen microbiome contains novel viruses that encode genes to promote microbial metabolism

Lichen thalli are formed through the symbiotic association of a filamentous fungus and photosynthetic green alga and/or cyanobacterium. Recent studies have revealed lichens also host highly diverse communities of secondary fungal and bacterial symbionts, yet few studies have examined the viral compo...

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Autores principales: Ponsero, Alise J., Hurwitz, Bonnie L., Magain, Nicolas, Miadlikowska, Jolanta, Lutzoni, François, U’Ren, Jana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723557/
https://www.ncbi.nlm.nih.gov/pubmed/37938275
http://dx.doi.org/10.1038/s43705-021-00060-w
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author Ponsero, Alise J.
Hurwitz, Bonnie L.
Magain, Nicolas
Miadlikowska, Jolanta
Lutzoni, François
U’Ren, Jana M.
author_facet Ponsero, Alise J.
Hurwitz, Bonnie L.
Magain, Nicolas
Miadlikowska, Jolanta
Lutzoni, François
U’Ren, Jana M.
author_sort Ponsero, Alise J.
collection PubMed
description Lichen thalli are formed through the symbiotic association of a filamentous fungus and photosynthetic green alga and/or cyanobacterium. Recent studies have revealed lichens also host highly diverse communities of secondary fungal and bacterial symbionts, yet few studies have examined the viral component within these complex symbioses. Here, we describe viral biodiversity and functions in cyanolichens collected from across North America and Europe. As current machine-learning viral-detection tools are not trained on complex eukaryotic metagenomes, we first developed efficient methods to remove eukaryotic reads prior to viral detection and a custom pipeline to validate viral contigs predicted with three machine-learning methods. Our resulting high-quality viral data illustrate that every cyanolichen thallus contains diverse viruses that are distinct from viruses in other terrestrial ecosystems. In addition to cyanobacteria, predicted viral hosts include other lichen-associated bacterial lineages and algae, although a large fraction of viral contigs had no host prediction. Functional annotation of cyanolichen viral sequences predicts numerous viral-encoded auxiliary metabolic genes (AMGs) involved in amino acid, nucleotide, and carbohydrate metabolism, including AMGs for secondary metabolism (antibiotics and antimicrobials) and fatty acid biosynthesis. Overall, the diversity of cyanolichen AMGs suggests that viruses may alter microbial interactions within these complex symbiotic assemblages.
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spelling pubmed-97235572023-01-04 Cyanolichen microbiome contains novel viruses that encode genes to promote microbial metabolism Ponsero, Alise J. Hurwitz, Bonnie L. Magain, Nicolas Miadlikowska, Jolanta Lutzoni, François U’Ren, Jana M. ISME Commun Brief Communication Lichen thalli are formed through the symbiotic association of a filamentous fungus and photosynthetic green alga and/or cyanobacterium. Recent studies have revealed lichens also host highly diverse communities of secondary fungal and bacterial symbionts, yet few studies have examined the viral component within these complex symbioses. Here, we describe viral biodiversity and functions in cyanolichens collected from across North America and Europe. As current machine-learning viral-detection tools are not trained on complex eukaryotic metagenomes, we first developed efficient methods to remove eukaryotic reads prior to viral detection and a custom pipeline to validate viral contigs predicted with three machine-learning methods. Our resulting high-quality viral data illustrate that every cyanolichen thallus contains diverse viruses that are distinct from viruses in other terrestrial ecosystems. In addition to cyanobacteria, predicted viral hosts include other lichen-associated bacterial lineages and algae, although a large fraction of viral contigs had no host prediction. Functional annotation of cyanolichen viral sequences predicts numerous viral-encoded auxiliary metabolic genes (AMGs) involved in amino acid, nucleotide, and carbohydrate metabolism, including AMGs for secondary metabolism (antibiotics and antimicrobials) and fatty acid biosynthesis. Overall, the diversity of cyanolichen AMGs suggests that viruses may alter microbial interactions within these complex symbiotic assemblages. Nature Publishing Group UK 2021-10-15 /pmc/articles/PMC9723557/ /pubmed/37938275 http://dx.doi.org/10.1038/s43705-021-00060-w 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 Brief Communication
Ponsero, Alise J.
Hurwitz, Bonnie L.
Magain, Nicolas
Miadlikowska, Jolanta
Lutzoni, François
U’Ren, Jana M.
Cyanolichen microbiome contains novel viruses that encode genes to promote microbial metabolism
title Cyanolichen microbiome contains novel viruses that encode genes to promote microbial metabolism
title_full Cyanolichen microbiome contains novel viruses that encode genes to promote microbial metabolism
title_fullStr Cyanolichen microbiome contains novel viruses that encode genes to promote microbial metabolism
title_full_unstemmed Cyanolichen microbiome contains novel viruses that encode genes to promote microbial metabolism
title_short Cyanolichen microbiome contains novel viruses that encode genes to promote microbial metabolism
title_sort cyanolichen microbiome contains novel viruses that encode genes to promote microbial metabolism
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723557/
https://www.ncbi.nlm.nih.gov/pubmed/37938275
http://dx.doi.org/10.1038/s43705-021-00060-w
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