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A lysin motif effector subverts chitin‐triggered immunity to facilitate arbuscular mycorrhizal symbiosis

Arbuscular mycorrhizal (AM) fungi greatly improve mineral uptake by host plants in nutrient‐depleted soil and can intracellularly colonize root cortex cells in the vast majority of higher plants. However, AM fungi possess common fungal cell wall components such as chitin that can be recognized by pl...

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Autores principales: Zeng, Tian, Rodriguez‐Moreno, Luis, Mansurkhodzaev, Artem, Wang, Peng, van den Berg, Willy, Gasciolli, Virginie, Cottaz, Sylvain, Fort, Sébastien, Thomma, Bart P. H. J., Bono, Jean‐Jacques, Bisseling, Ton, Limpens, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916333/
https://www.ncbi.nlm.nih.gov/pubmed/31596956
http://dx.doi.org/10.1111/nph.16245
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author Zeng, Tian
Rodriguez‐Moreno, Luis
Mansurkhodzaev, Artem
Wang, Peng
van den Berg, Willy
Gasciolli, Virginie
Cottaz, Sylvain
Fort, Sébastien
Thomma, Bart P. H. J.
Bono, Jean‐Jacques
Bisseling, Ton
Limpens, Erik
author_facet Zeng, Tian
Rodriguez‐Moreno, Luis
Mansurkhodzaev, Artem
Wang, Peng
van den Berg, Willy
Gasciolli, Virginie
Cottaz, Sylvain
Fort, Sébastien
Thomma, Bart P. H. J.
Bono, Jean‐Jacques
Bisseling, Ton
Limpens, Erik
author_sort Zeng, Tian
collection PubMed
description Arbuscular mycorrhizal (AM) fungi greatly improve mineral uptake by host plants in nutrient‐depleted soil and can intracellularly colonize root cortex cells in the vast majority of higher plants. However, AM fungi possess common fungal cell wall components such as chitin that can be recognized by plant chitin receptors to trigger immune responses, raising the question as to how AM fungi effectively evade chitin‐triggered immune responses during symbiosis. In this study, we characterize a secreted lysin motif (LysM) effector identified from the model AM fungal species Rhizophagus irregularis, called RiSLM. RiSLM is one of the highest expressed effector proteins in intraradical mycelium during the symbiosis. In vitro binding assays show that RiSLM binds chitin‐oligosaccharides and can protect fungal cell walls from chitinases. Moreover, RiSLM efficiently interferes with chitin‐triggered immune responses, such as defence gene induction and reactive oxygen species production in Medicago truncatula. Although RiSLM also binds to symbiotic (lipo)chitooligosaccharides it does not interfere significantly with symbiotic signalling in Medicago. Host‐induced gene silencing of RiSLM greatly reduces fungal colonization levels. Taken together, our results reveal a key role for AM fungal LysM effectors to subvert chitin‐triggered immunity in symbiosis, pointing to a common role for LysM effectors in both symbiotic and pathogenic fungi.
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spelling pubmed-69163332019-12-17 A lysin motif effector subverts chitin‐triggered immunity to facilitate arbuscular mycorrhizal symbiosis Zeng, Tian Rodriguez‐Moreno, Luis Mansurkhodzaev, Artem Wang, Peng van den Berg, Willy Gasciolli, Virginie Cottaz, Sylvain Fort, Sébastien Thomma, Bart P. H. J. Bono, Jean‐Jacques Bisseling, Ton Limpens, Erik New Phytol Research Arbuscular mycorrhizal (AM) fungi greatly improve mineral uptake by host plants in nutrient‐depleted soil and can intracellularly colonize root cortex cells in the vast majority of higher plants. However, AM fungi possess common fungal cell wall components such as chitin that can be recognized by plant chitin receptors to trigger immune responses, raising the question as to how AM fungi effectively evade chitin‐triggered immune responses during symbiosis. In this study, we characterize a secreted lysin motif (LysM) effector identified from the model AM fungal species Rhizophagus irregularis, called RiSLM. RiSLM is one of the highest expressed effector proteins in intraradical mycelium during the symbiosis. In vitro binding assays show that RiSLM binds chitin‐oligosaccharides and can protect fungal cell walls from chitinases. Moreover, RiSLM efficiently interferes with chitin‐triggered immune responses, such as defence gene induction and reactive oxygen species production in Medicago truncatula. Although RiSLM also binds to symbiotic (lipo)chitooligosaccharides it does not interfere significantly with symbiotic signalling in Medicago. Host‐induced gene silencing of RiSLM greatly reduces fungal colonization levels. Taken together, our results reveal a key role for AM fungal LysM effectors to subvert chitin‐triggered immunity in symbiosis, pointing to a common role for LysM effectors in both symbiotic and pathogenic fungi. John Wiley and Sons Inc. 2019-11-23 2020-01 /pmc/articles/PMC6916333/ /pubmed/31596956 http://dx.doi.org/10.1111/nph.16245 Text en © 2019 The Authors. New Phytologist © 2019 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Zeng, Tian
Rodriguez‐Moreno, Luis
Mansurkhodzaev, Artem
Wang, Peng
van den Berg, Willy
Gasciolli, Virginie
Cottaz, Sylvain
Fort, Sébastien
Thomma, Bart P. H. J.
Bono, Jean‐Jacques
Bisseling, Ton
Limpens, Erik
A lysin motif effector subverts chitin‐triggered immunity to facilitate arbuscular mycorrhizal symbiosis
title A lysin motif effector subverts chitin‐triggered immunity to facilitate arbuscular mycorrhizal symbiosis
title_full A lysin motif effector subverts chitin‐triggered immunity to facilitate arbuscular mycorrhizal symbiosis
title_fullStr A lysin motif effector subverts chitin‐triggered immunity to facilitate arbuscular mycorrhizal symbiosis
title_full_unstemmed A lysin motif effector subverts chitin‐triggered immunity to facilitate arbuscular mycorrhizal symbiosis
title_short A lysin motif effector subverts chitin‐triggered immunity to facilitate arbuscular mycorrhizal symbiosis
title_sort lysin motif effector subverts chitin‐triggered immunity to facilitate arbuscular mycorrhizal symbiosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916333/
https://www.ncbi.nlm.nih.gov/pubmed/31596956
http://dx.doi.org/10.1111/nph.16245
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