Cargando…

The virome from a collection of endomycorrhizal fungi reveals new viral taxa with unprecedented genome organization

Mutualistic plant-associated fungi are recognized as important drivers in plant evolution, diversity, and health. The discovery that mycoviruses can take part and play important roles in symbiotic tripartite interactions has prompted us to study the viromes associated with a collection of ericoid an...

Descripción completa

Detalles Bibliográficos
Autores principales: Sutela, Suvi, Forgia, Marco, Vainio, Eeva J, Chiapello, Marco, Daghino, Stefania, Vallino, Marta, Martino, Elena, Girlanda, Mariangela, Perotto, Silvia, Turina, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724248/
https://www.ncbi.nlm.nih.gov/pubmed/33324490
http://dx.doi.org/10.1093/ve/veaa076
_version_ 1783620505878659072
author Sutela, Suvi
Forgia, Marco
Vainio, Eeva J
Chiapello, Marco
Daghino, Stefania
Vallino, Marta
Martino, Elena
Girlanda, Mariangela
Perotto, Silvia
Turina, Massimo
author_facet Sutela, Suvi
Forgia, Marco
Vainio, Eeva J
Chiapello, Marco
Daghino, Stefania
Vallino, Marta
Martino, Elena
Girlanda, Mariangela
Perotto, Silvia
Turina, Massimo
author_sort Sutela, Suvi
collection PubMed
description Mutualistic plant-associated fungi are recognized as important drivers in plant evolution, diversity, and health. The discovery that mycoviruses can take part and play important roles in symbiotic tripartite interactions has prompted us to study the viromes associated with a collection of ericoid and orchid mycorrhizal (ERM and ORM, respectively) fungi. Our study, based on high-throughput sequencing of transcriptomes (RNAseq) from fungal isolates grown in axenic cultures, revealed in both ERM and ORM fungi the presence of new mycoviruses closely related to already classified virus taxa, but also new viruses that expand the boundaries of characterized RNA virus diversity to previously undescribed evolutionary trajectories. In ERM fungi, we provide first evidence of a bipartite virus, distantly related to narnaviruses, that splits the RNA-dependent RNA polymerase (RdRP) palm domain into two distinct proteins, encoded by each of the two segments. Furthermore, in one isolate of the ORM fungus Tulasnella spp. we detected a 12 kb genomic fragment coding for an RdRP with features of bunyavirus-like RdRPs. However, this 12 kb genomic RNA has the unique features, for Bunyavirales members, of being tri-cistronic and carrying ORFs for the putative RdRP and putative nucleocapsid in ambisense orientation on the same genomic RNA. Finally, a number of ORM fungal isolates harbored a group of ambisense bicistronic viruses with a genomic size of around 5 kb, where we could identify a putative RdRP palm domain that has some features of plus strand RNA viruses; these new viruses may represent a new lineage in the Riboviria, as they could not be reliably assigned to any of the branches in the recently derived monophyletic tree that includes most viruses with an RNA genome.
format Online
Article
Text
id pubmed-7724248
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77242482020-12-14 The virome from a collection of endomycorrhizal fungi reveals new viral taxa with unprecedented genome organization Sutela, Suvi Forgia, Marco Vainio, Eeva J Chiapello, Marco Daghino, Stefania Vallino, Marta Martino, Elena Girlanda, Mariangela Perotto, Silvia Turina, Massimo Virus Evol Research Article Mutualistic plant-associated fungi are recognized as important drivers in plant evolution, diversity, and health. The discovery that mycoviruses can take part and play important roles in symbiotic tripartite interactions has prompted us to study the viromes associated with a collection of ericoid and orchid mycorrhizal (ERM and ORM, respectively) fungi. Our study, based on high-throughput sequencing of transcriptomes (RNAseq) from fungal isolates grown in axenic cultures, revealed in both ERM and ORM fungi the presence of new mycoviruses closely related to already classified virus taxa, but also new viruses that expand the boundaries of characterized RNA virus diversity to previously undescribed evolutionary trajectories. In ERM fungi, we provide first evidence of a bipartite virus, distantly related to narnaviruses, that splits the RNA-dependent RNA polymerase (RdRP) palm domain into two distinct proteins, encoded by each of the two segments. Furthermore, in one isolate of the ORM fungus Tulasnella spp. we detected a 12 kb genomic fragment coding for an RdRP with features of bunyavirus-like RdRPs. However, this 12 kb genomic RNA has the unique features, for Bunyavirales members, of being tri-cistronic and carrying ORFs for the putative RdRP and putative nucleocapsid in ambisense orientation on the same genomic RNA. Finally, a number of ORM fungal isolates harbored a group of ambisense bicistronic viruses with a genomic size of around 5 kb, where we could identify a putative RdRP palm domain that has some features of plus strand RNA viruses; these new viruses may represent a new lineage in the Riboviria, as they could not be reliably assigned to any of the branches in the recently derived monophyletic tree that includes most viruses with an RNA genome. Oxford University Press 2020-10-08 /pmc/articles/PMC7724248/ /pubmed/33324490 http://dx.doi.org/10.1093/ve/veaa076 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Sutela, Suvi
Forgia, Marco
Vainio, Eeva J
Chiapello, Marco
Daghino, Stefania
Vallino, Marta
Martino, Elena
Girlanda, Mariangela
Perotto, Silvia
Turina, Massimo
The virome from a collection of endomycorrhizal fungi reveals new viral taxa with unprecedented genome organization
title The virome from a collection of endomycorrhizal fungi reveals new viral taxa with unprecedented genome organization
title_full The virome from a collection of endomycorrhizal fungi reveals new viral taxa with unprecedented genome organization
title_fullStr The virome from a collection of endomycorrhizal fungi reveals new viral taxa with unprecedented genome organization
title_full_unstemmed The virome from a collection of endomycorrhizal fungi reveals new viral taxa with unprecedented genome organization
title_short The virome from a collection of endomycorrhizal fungi reveals new viral taxa with unprecedented genome organization
title_sort virome from a collection of endomycorrhizal fungi reveals new viral taxa with unprecedented genome organization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724248/
https://www.ncbi.nlm.nih.gov/pubmed/33324490
http://dx.doi.org/10.1093/ve/veaa076
work_keys_str_mv AT sutelasuvi theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT forgiamarco theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT vainioeevaj theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT chiapellomarco theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT daghinostefania theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT vallinomarta theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT martinoelena theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT girlandamariangela theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT perottosilvia theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT turinamassimo theviromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT sutelasuvi viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT forgiamarco viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT vainioeevaj viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT chiapellomarco viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT daghinostefania viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT vallinomarta viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT martinoelena viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT girlandamariangela viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT perottosilvia viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization
AT turinamassimo viromefromacollectionofendomycorrhizalfungirevealsnewviraltaxawithunprecedentedgenomeorganization