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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-9292583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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