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Role of Dicer-Dependent RNA Interference in Regulating Mycoparasitic Interactions

Dicer-like proteins (DCLs) play a vital role in RNA interference (RNAi), by cleaving RNA filament into small RNAs. Although DCL-mediated RNAi can regulate interspecific communication between pathogenic/mutualistic organisms and their hosts, its role in mycoparasitic interactions is yet to be investi...

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Autores principales: Piombo, Edoardo, Vetukuri, Ramesh R., Broberg, Anders, Kalyandurg, Pruthvi B., Kushwaha, Sandeep, Funck Jensen, Dan, Karlsson, Magnus, Dubey, Mukesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557909/
https://www.ncbi.nlm.nih.gov/pubmed/34549988
http://dx.doi.org/10.1128/Spectrum.01099-21
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author Piombo, Edoardo
Vetukuri, Ramesh R.
Broberg, Anders
Kalyandurg, Pruthvi B.
Kushwaha, Sandeep
Funck Jensen, Dan
Karlsson, Magnus
Dubey, Mukesh
author_facet Piombo, Edoardo
Vetukuri, Ramesh R.
Broberg, Anders
Kalyandurg, Pruthvi B.
Kushwaha, Sandeep
Funck Jensen, Dan
Karlsson, Magnus
Dubey, Mukesh
author_sort Piombo, Edoardo
collection PubMed
description Dicer-like proteins (DCLs) play a vital role in RNA interference (RNAi), by cleaving RNA filament into small RNAs. Although DCL-mediated RNAi can regulate interspecific communication between pathogenic/mutualistic organisms and their hosts, its role in mycoparasitic interactions is yet to be investigated. In this study, we deleted dcl genes in the mycoparasitic fungus Clonostachys rosea and characterize the functions of DCL-dependent RNAi in mycoparasitism. Deletion of dcl2 resulted in a mutant with reduced secondary metabolite production, antagonism toward the plant-pathogenic fungus Botrytis cinerea, and reduced ability to control Fusarium foot rot disease on wheat, caused by Fusarium graminearum. Transcriptome sequencing of the in vitro interaction between the C. rosea Δdcl2 strain and B. cinerea or F. graminearum identified the downregulation of genes coding for transcription factors, membrane transporters, hydrolytic enzymes, and secondary metabolites biosynthesis enzymes putatively involved in antagonistic interactions, in comparison with the C. rosea wild-type interaction. A total of 61 putative novel microRNA-like RNAs (milRNAs) were identified in C. rosea, and 11 were downregulated in the Δdcl2 mutant. In addition to putative endogenous gene targets, these milRNAs were predicted to target B. cinerea and F. graminearum virulence factor genes, which showed an increased expression during interaction with the Δdcl2 mutant incapable of producing the targeting milRNAs. In summary, this study constitutes the first step in elucidating the role of RNAi in mycoparasitic interactions, with important implications for biological control of plant diseases, and poses the base for future studies focusing on the role of cross-species RNAi regulating mycoparasitic interactions. IMPORTANCE Small RNAs mediated RNA interference (RNAi) known to regulate several biological processes. Dicer-like endoribonucleases (DCLs) play a vital role in the RNAi pathway by generating sRNAs. In this study, we investigated a role of DCL-mediated RNAi in interference interactions between mycoparasitic fungus Clonostachys rosea and the two fungal pathogens Botrytis cinerea and Fusarium graminearum (here called mycohosts). We found that the dcl mutants were not able to produce 11 sRNAs predicted to finetune the regulatory network of genes known to be involved in production of hydrolytic enzymes, antifungal compounds, and membrane transporters needed for antagonistic action of C. rosea. We also found C. rosea sRNAs putatively targeting known virulence factors in the mycohosts, indicating RNAi-mediated cross-species communication. Our study expanded the understanding of underlying mechanisms of cross-species communication during interference interactions and poses a base for future works studying the role of DCL-based cross-species RNAi in fungal interactions.
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spelling pubmed-85579092021-11-08 Role of Dicer-Dependent RNA Interference in Regulating Mycoparasitic Interactions Piombo, Edoardo Vetukuri, Ramesh R. Broberg, Anders Kalyandurg, Pruthvi B. Kushwaha, Sandeep Funck Jensen, Dan Karlsson, Magnus Dubey, Mukesh Microbiol Spectr Research Article Dicer-like proteins (DCLs) play a vital role in RNA interference (RNAi), by cleaving RNA filament into small RNAs. Although DCL-mediated RNAi can regulate interspecific communication between pathogenic/mutualistic organisms and their hosts, its role in mycoparasitic interactions is yet to be investigated. In this study, we deleted dcl genes in the mycoparasitic fungus Clonostachys rosea and characterize the functions of DCL-dependent RNAi in mycoparasitism. Deletion of dcl2 resulted in a mutant with reduced secondary metabolite production, antagonism toward the plant-pathogenic fungus Botrytis cinerea, and reduced ability to control Fusarium foot rot disease on wheat, caused by Fusarium graminearum. Transcriptome sequencing of the in vitro interaction between the C. rosea Δdcl2 strain and B. cinerea or F. graminearum identified the downregulation of genes coding for transcription factors, membrane transporters, hydrolytic enzymes, and secondary metabolites biosynthesis enzymes putatively involved in antagonistic interactions, in comparison with the C. rosea wild-type interaction. A total of 61 putative novel microRNA-like RNAs (milRNAs) were identified in C. rosea, and 11 were downregulated in the Δdcl2 mutant. In addition to putative endogenous gene targets, these milRNAs were predicted to target B. cinerea and F. graminearum virulence factor genes, which showed an increased expression during interaction with the Δdcl2 mutant incapable of producing the targeting milRNAs. In summary, this study constitutes the first step in elucidating the role of RNAi in mycoparasitic interactions, with important implications for biological control of plant diseases, and poses the base for future studies focusing on the role of cross-species RNAi regulating mycoparasitic interactions. IMPORTANCE Small RNAs mediated RNA interference (RNAi) known to regulate several biological processes. Dicer-like endoribonucleases (DCLs) play a vital role in the RNAi pathway by generating sRNAs. In this study, we investigated a role of DCL-mediated RNAi in interference interactions between mycoparasitic fungus Clonostachys rosea and the two fungal pathogens Botrytis cinerea and Fusarium graminearum (here called mycohosts). We found that the dcl mutants were not able to produce 11 sRNAs predicted to finetune the regulatory network of genes known to be involved in production of hydrolytic enzymes, antifungal compounds, and membrane transporters needed for antagonistic action of C. rosea. We also found C. rosea sRNAs putatively targeting known virulence factors in the mycohosts, indicating RNAi-mediated cross-species communication. Our study expanded the understanding of underlying mechanisms of cross-species communication during interference interactions and poses a base for future works studying the role of DCL-based cross-species RNAi in fungal interactions. American Society for Microbiology 2021-09-22 /pmc/articles/PMC8557909/ /pubmed/34549988 http://dx.doi.org/10.1128/Spectrum.01099-21 Text en Copyright © 2021 Piombo et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Piombo, Edoardo
Vetukuri, Ramesh R.
Broberg, Anders
Kalyandurg, Pruthvi B.
Kushwaha, Sandeep
Funck Jensen, Dan
Karlsson, Magnus
Dubey, Mukesh
Role of Dicer-Dependent RNA Interference in Regulating Mycoparasitic Interactions
title Role of Dicer-Dependent RNA Interference in Regulating Mycoparasitic Interactions
title_full Role of Dicer-Dependent RNA Interference in Regulating Mycoparasitic Interactions
title_fullStr Role of Dicer-Dependent RNA Interference in Regulating Mycoparasitic Interactions
title_full_unstemmed Role of Dicer-Dependent RNA Interference in Regulating Mycoparasitic Interactions
title_short Role of Dicer-Dependent RNA Interference in Regulating Mycoparasitic Interactions
title_sort role of dicer-dependent rna interference in regulating mycoparasitic interactions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557909/
https://www.ncbi.nlm.nih.gov/pubmed/34549988
http://dx.doi.org/10.1128/Spectrum.01099-21
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