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An Arabidopsis downy mildew non-RxLR effector suppresses induced plant cell death to promote biotroph infection
Our understanding of obligate biotrophic pathogens is limited by lack of knowledge concerning the molecular function of virulence factors. We established Arabidopsis host-induced gene silencing (HIGS) to explore gene functions of Hyaloperonospora arabidopsidis, including CYSTEINE-RICH PROTEIN (HaCR)...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7853606/ https://www.ncbi.nlm.nih.gov/pubmed/33063828 http://dx.doi.org/10.1093/jxb/eraa472 |
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author | Dunker, Florian Oberkofler, Lorenz Lederer, Bernhard Trutzenberg, Adriana Weiberg, Arne |
author_facet | Dunker, Florian Oberkofler, Lorenz Lederer, Bernhard Trutzenberg, Adriana Weiberg, Arne |
author_sort | Dunker, Florian |
collection | PubMed |
description | Our understanding of obligate biotrophic pathogens is limited by lack of knowledge concerning the molecular function of virulence factors. We established Arabidopsis host-induced gene silencing (HIGS) to explore gene functions of Hyaloperonospora arabidopsidis, including CYSTEINE-RICH PROTEIN (HaCR)1, a potential secreted effector gene of this obligate biotrophic pathogen. HaCR1 HIGS resulted in H. arabidopsidis-induced local plant cell death and reduced pathogen reproduction. We functionally characterized HaCR1 by ectopic expression in Nicotiana benthamiana. HaCR1 was capable of inhibiting effector-triggered plant cell death. Consistent with this, HaCR1 expression in N. benthamiana led to stronger disease symptoms caused by the hemibiotrophic oomycete pathogen Phytophthora capsici, but reduced disease symptoms caused by the necrotrophic fungal pathogen Botrytis cinerea. Expressing HaCR1 in transgenic Arabidopsis confirmed higher susceptibility to H. arabidopsidis and to the bacterial hemibiotrophic pathogen Pseudomonas syringae. Increased H. arabidopsidis infection was in accordance with reduced PATHOGENESIS RELATED (PR)1 induction. Expression of full-length HaCR1 was required for its function, which was lost if the signal peptide was deleted, suggesting its site of action in the plant apoplast. This study provides phytopathological and molecular evidence for the importance of this widespread, but largely unexplored class of non-RxLR effectors in biotrophic oomycetes. |
format | Online Article Text |
id | pubmed-7853606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78536062021-02-04 An Arabidopsis downy mildew non-RxLR effector suppresses induced plant cell death to promote biotroph infection Dunker, Florian Oberkofler, Lorenz Lederer, Bernhard Trutzenberg, Adriana Weiberg, Arne J Exp Bot Research Paper Our understanding of obligate biotrophic pathogens is limited by lack of knowledge concerning the molecular function of virulence factors. We established Arabidopsis host-induced gene silencing (HIGS) to explore gene functions of Hyaloperonospora arabidopsidis, including CYSTEINE-RICH PROTEIN (HaCR)1, a potential secreted effector gene of this obligate biotrophic pathogen. HaCR1 HIGS resulted in H. arabidopsidis-induced local plant cell death and reduced pathogen reproduction. We functionally characterized HaCR1 by ectopic expression in Nicotiana benthamiana. HaCR1 was capable of inhibiting effector-triggered plant cell death. Consistent with this, HaCR1 expression in N. benthamiana led to stronger disease symptoms caused by the hemibiotrophic oomycete pathogen Phytophthora capsici, but reduced disease symptoms caused by the necrotrophic fungal pathogen Botrytis cinerea. Expressing HaCR1 in transgenic Arabidopsis confirmed higher susceptibility to H. arabidopsidis and to the bacterial hemibiotrophic pathogen Pseudomonas syringae. Increased H. arabidopsidis infection was in accordance with reduced PATHOGENESIS RELATED (PR)1 induction. Expression of full-length HaCR1 was required for its function, which was lost if the signal peptide was deleted, suggesting its site of action in the plant apoplast. This study provides phytopathological and molecular evidence for the importance of this widespread, but largely unexplored class of non-RxLR effectors in biotrophic oomycetes. Oxford University Press 2020-10-16 /pmc/articles/PMC7853606/ /pubmed/33063828 http://dx.doi.org/10.1093/jxb/eraa472 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Dunker, Florian Oberkofler, Lorenz Lederer, Bernhard Trutzenberg, Adriana Weiberg, Arne An Arabidopsis downy mildew non-RxLR effector suppresses induced plant cell death to promote biotroph infection |
title | An Arabidopsis downy mildew non-RxLR effector suppresses induced plant cell death to promote biotroph infection |
title_full | An Arabidopsis downy mildew non-RxLR effector suppresses induced plant cell death to promote biotroph infection |
title_fullStr | An Arabidopsis downy mildew non-RxLR effector suppresses induced plant cell death to promote biotroph infection |
title_full_unstemmed | An Arabidopsis downy mildew non-RxLR effector suppresses induced plant cell death to promote biotroph infection |
title_short | An Arabidopsis downy mildew non-RxLR effector suppresses induced plant cell death to promote biotroph infection |
title_sort | arabidopsis downy mildew non-rxlr effector suppresses induced plant cell death to promote biotroph infection |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7853606/ https://www.ncbi.nlm.nih.gov/pubmed/33063828 http://dx.doi.org/10.1093/jxb/eraa472 |
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