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Cross-Kingdom RNAi of Pathogen Effectors Leads to Quantitative Adult Plant Resistance in Wheat

Cross-kingdom RNA interference (RNAi) is a biological process allowing plants to transfer small regulatory RNAs to invading pathogens to trigger the silencing of target virulence genes. Transient assays in cereal powdery mildews suggest that silencing of one or two effectors could lead to near loss...

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Autores principales: Schaefer, Luisa Katharina, Parlange, Francis, Buchmann, Gabriele, Jung, Esther, Wehrli, Andreas, Herren, Gerhard, Müller, Marion Claudia, Stehlin, Jonas, Schmid, Roman, Wicker, Thomas, Keller, Beat, Bourras, Salim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076181/
https://www.ncbi.nlm.nih.gov/pubmed/32211008
http://dx.doi.org/10.3389/fpls.2020.00253
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author Schaefer, Luisa Katharina
Parlange, Francis
Buchmann, Gabriele
Jung, Esther
Wehrli, Andreas
Herren, Gerhard
Müller, Marion Claudia
Stehlin, Jonas
Schmid, Roman
Wicker, Thomas
Keller, Beat
Bourras, Salim
author_facet Schaefer, Luisa Katharina
Parlange, Francis
Buchmann, Gabriele
Jung, Esther
Wehrli, Andreas
Herren, Gerhard
Müller, Marion Claudia
Stehlin, Jonas
Schmid, Roman
Wicker, Thomas
Keller, Beat
Bourras, Salim
author_sort Schaefer, Luisa Katharina
collection PubMed
description Cross-kingdom RNA interference (RNAi) is a biological process allowing plants to transfer small regulatory RNAs to invading pathogens to trigger the silencing of target virulence genes. Transient assays in cereal powdery mildews suggest that silencing of one or two effectors could lead to near loss of virulence, but evidence from stable RNAi lines is lacking. We established transient host-induced gene silencing (HIGS) in wheat, and demonstrate that targeting an essential housekeeping gene in the wheat powdery mildew pathogen (Blumeria graminis f. sp. tritici) results in significant reduction of virulence at an early stage of infection. We generated stable transgenic RNAi wheat lines encoding a HIGS construct simultaneously silencing three B.g. tritici effectors including SvrPm3(a1/f1), a virulence factor involved in the suppression of the Pm3 powdery mildew resistance gene. We show that all targeted effectors are effectively downregulated by HIGS, resulting in reduced fungal virulence on adult wheat plants. Our findings demonstrate that stable HIGS of effector genes can lead to quantitative gain of resistance without major pleiotropic effects in wheat.
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spelling pubmed-70761812020-03-24 Cross-Kingdom RNAi of Pathogen Effectors Leads to Quantitative Adult Plant Resistance in Wheat Schaefer, Luisa Katharina Parlange, Francis Buchmann, Gabriele Jung, Esther Wehrli, Andreas Herren, Gerhard Müller, Marion Claudia Stehlin, Jonas Schmid, Roman Wicker, Thomas Keller, Beat Bourras, Salim Front Plant Sci Plant Science Cross-kingdom RNA interference (RNAi) is a biological process allowing plants to transfer small regulatory RNAs to invading pathogens to trigger the silencing of target virulence genes. Transient assays in cereal powdery mildews suggest that silencing of one or two effectors could lead to near loss of virulence, but evidence from stable RNAi lines is lacking. We established transient host-induced gene silencing (HIGS) in wheat, and demonstrate that targeting an essential housekeeping gene in the wheat powdery mildew pathogen (Blumeria graminis f. sp. tritici) results in significant reduction of virulence at an early stage of infection. We generated stable transgenic RNAi wheat lines encoding a HIGS construct simultaneously silencing three B.g. tritici effectors including SvrPm3(a1/f1), a virulence factor involved in the suppression of the Pm3 powdery mildew resistance gene. We show that all targeted effectors are effectively downregulated by HIGS, resulting in reduced fungal virulence on adult wheat plants. Our findings demonstrate that stable HIGS of effector genes can lead to quantitative gain of resistance without major pleiotropic effects in wheat. Frontiers Media S.A. 2020-03-10 /pmc/articles/PMC7076181/ /pubmed/32211008 http://dx.doi.org/10.3389/fpls.2020.00253 Text en Copyright © 2020 Schaefer, Parlange, Buchmann, Jung, Wehrli, Herren, Müller, Stehlin, Schmid, Wicker, Keller and Bourras. http://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 Plant Science
Schaefer, Luisa Katharina
Parlange, Francis
Buchmann, Gabriele
Jung, Esther
Wehrli, Andreas
Herren, Gerhard
Müller, Marion Claudia
Stehlin, Jonas
Schmid, Roman
Wicker, Thomas
Keller, Beat
Bourras, Salim
Cross-Kingdom RNAi of Pathogen Effectors Leads to Quantitative Adult Plant Resistance in Wheat
title Cross-Kingdom RNAi of Pathogen Effectors Leads to Quantitative Adult Plant Resistance in Wheat
title_full Cross-Kingdom RNAi of Pathogen Effectors Leads to Quantitative Adult Plant Resistance in Wheat
title_fullStr Cross-Kingdom RNAi of Pathogen Effectors Leads to Quantitative Adult Plant Resistance in Wheat
title_full_unstemmed Cross-Kingdom RNAi of Pathogen Effectors Leads to Quantitative Adult Plant Resistance in Wheat
title_short Cross-Kingdom RNAi of Pathogen Effectors Leads to Quantitative Adult Plant Resistance in Wheat
title_sort cross-kingdom rnai of pathogen effectors leads to quantitative adult plant resistance in wheat
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076181/
https://www.ncbi.nlm.nih.gov/pubmed/32211008
http://dx.doi.org/10.3389/fpls.2020.00253
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