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Insect eggs trigger systemic acquired resistance against a fungal and an oomycete pathogen

Plants are able to detect insect eggs deposited on leaves. In Arabidopsis, eggs of the butterfly species Pieris brassicae (common name large white) induce plant defenses and activate the salicylic acid (SA) pathway. We previously discovered that oviposition triggers a systemic acquired resistance (S...

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Autores principales: Alfonso, Esteban, Stahl, Elia, Glauser, Gaétan, Bellani, Etienne, Raaymakers, Tom M., Van den Ackerveken, Guido, Zeier, Jürgen, Reymond, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292583/
https://www.ncbi.nlm.nih.gov/pubmed/34510462
http://dx.doi.org/10.1111/nph.17732
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author Alfonso, Esteban
Stahl, Elia
Glauser, Gaétan
Bellani, Etienne
Raaymakers, Tom M.
Van den Ackerveken, Guido
Zeier, Jürgen
Reymond, Philippe
author_facet Alfonso, Esteban
Stahl, Elia
Glauser, Gaétan
Bellani, Etienne
Raaymakers, Tom M.
Van den Ackerveken, Guido
Zeier, Jürgen
Reymond, Philippe
author_sort Alfonso, Esteban
collection PubMed
description Plants are able to detect insect eggs deposited on leaves. In Arabidopsis, eggs of the butterfly species Pieris brassicae (common name large white) induce plant defenses and activate the salicylic acid (SA) pathway. We previously discovered that oviposition triggers a systemic acquired resistance (SAR) against the bacterial hemibiotroph pathogen Pseudomonas syringae. Here, we show that insect eggs or treatment with egg extract (EE) induce SAR against the fungal necrotroph Botrytis cinerea BMM and the oomycete pathogen Hyaloperonospora arabidopsidis Noco2. This response is abolished in ics1, ald1 and fmo1, indicating that the SA pathway and the N‐hydroxypipecolic acid (NHP) pathway are involved. Establishment of EE‐induced SAR in distal leaves potentially involves tryptophan‐derived metabolites, including camalexin. Indeed, SAR is abolished in the biosynthesis mutants cyp79B2 cyp79B3, cyp71a12 cyp71a13 and pad3‐1, and camalexin is toxic to B. cinerea in vitro. This study reveals an interesting mechanism by which lepidopteran eggs interfere with plant–pathogen interactions.
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spelling pubmed-92925832022-07-20 Insect eggs trigger systemic acquired resistance against a fungal and an oomycete pathogen Alfonso, Esteban Stahl, Elia Glauser, Gaétan Bellani, Etienne Raaymakers, Tom M. Van den Ackerveken, Guido Zeier, Jürgen Reymond, Philippe New Phytol Research Plants are able to detect insect eggs deposited on leaves. In Arabidopsis, eggs of the butterfly species Pieris brassicae (common name large white) induce plant defenses and activate the salicylic acid (SA) pathway. We previously discovered that oviposition triggers a systemic acquired resistance (SAR) against the bacterial hemibiotroph pathogen Pseudomonas syringae. Here, we show that insect eggs or treatment with egg extract (EE) induce SAR against the fungal necrotroph Botrytis cinerea BMM and the oomycete pathogen Hyaloperonospora arabidopsidis Noco2. This response is abolished in ics1, ald1 and fmo1, indicating that the SA pathway and the N‐hydroxypipecolic acid (NHP) pathway are involved. Establishment of EE‐induced SAR in distal leaves potentially involves tryptophan‐derived metabolites, including camalexin. Indeed, SAR is abolished in the biosynthesis mutants cyp79B2 cyp79B3, cyp71a12 cyp71a13 and pad3‐1, and camalexin is toxic to B. cinerea in vitro. This study reveals an interesting mechanism by which lepidopteran eggs interfere with plant–pathogen interactions. John Wiley and Sons Inc. 2021-09-25 2021-12 /pmc/articles/PMC9292583/ /pubmed/34510462 http://dx.doi.org/10.1111/nph.17732 Text en © 2021 The Authors. New Phytologist © 2021 New Phytologist Foundation https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research
Alfonso, Esteban
Stahl, Elia
Glauser, Gaétan
Bellani, Etienne
Raaymakers, Tom M.
Van den Ackerveken, Guido
Zeier, Jürgen
Reymond, Philippe
Insect eggs trigger systemic acquired resistance against a fungal and an oomycete pathogen
title Insect eggs trigger systemic acquired resistance against a fungal and an oomycete pathogen
title_full Insect eggs trigger systemic acquired resistance against a fungal and an oomycete pathogen
title_fullStr Insect eggs trigger systemic acquired resistance against a fungal and an oomycete pathogen
title_full_unstemmed Insect eggs trigger systemic acquired resistance against a fungal and an oomycete pathogen
title_short Insect eggs trigger systemic acquired resistance against a fungal and an oomycete pathogen
title_sort insect eggs trigger systemic acquired resistance against a fungal and an oomycete pathogen
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292583/
https://www.ncbi.nlm.nih.gov/pubmed/34510462
http://dx.doi.org/10.1111/nph.17732
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