Cargando…
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...
Autores principales: | , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783507174301892608 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7076181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT schaeferluisakatharina crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT parlangefrancis crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT buchmanngabriele crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT jungesther crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT wehrliandreas crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT herrengerhard crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT mullermarionclaudia crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT stehlinjonas crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT schmidroman crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT wickerthomas crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT kellerbeat crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat AT bourrassalim crosskingdomrnaiofpathogeneffectorsleadstoquantitativeadultplantresistanceinwheat |