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d‐Lactic acid secreted by Chlorella fusca primes pattern‐triggered immunity against Pseudomonas syringae in Arabidopsis

Biological control agents including microbes and their products have been studied as sustainable crop protection strategies. Although aquatic microalgae have been recently introduced as a biological control agent, the underlying molecular mechanisms are largely unknown. The aim of the present study...

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Autores principales: Lee, Sang‐Moo, Kim, Seon‐Kyu, Lee, Nakyeong, Ahn, Chi‐Yong, Ryu, Choong‐Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318130/
https://www.ncbi.nlm.nih.gov/pubmed/31869481
http://dx.doi.org/10.1111/tpj.14661
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author Lee, Sang‐Moo
Kim, Seon‐Kyu
Lee, Nakyeong
Ahn, Chi‐Yong
Ryu, Choong‐Min
author_facet Lee, Sang‐Moo
Kim, Seon‐Kyu
Lee, Nakyeong
Ahn, Chi‐Yong
Ryu, Choong‐Min
author_sort Lee, Sang‐Moo
collection PubMed
description Biological control agents including microbes and their products have been studied as sustainable crop protection strategies. Although aquatic microalgae have been recently introduced as a biological control agent, the underlying molecular mechanisms are largely unknown. The aim of the present study was to investigate the molecular mechanisms underlying biological control by microalga Chlorella fusca. Foliar application of C. fusca elicits induced resistance in Arabidopsis thaliana against Pseudomonas syringae pv. tomato DC3000 that activates plant immunity rather than direct antagonism. To understand the basis of C. fusca‐triggered induced resistance at the transcriptional level, we conducted RNA sequencing (RNA‐seq) analysis. RNA‐seq data showed that, upon pathogen inoculation, C. fusca treatment primed the expression of cysteine‐rich receptor‐like kinases, WRKY transcription factor genes, and salicylic acid and jasmonic acid signalling‐related genes. Intriguingly, the application of C. fusca primed pathogen‐associated molecular pattern ‐triggered immunity, characterized by reactive oxygen species burst and callose deposition, upon flagellin 22 treatment. The attempts to find C. fusca determinants allowed us to identify d‐lactic acid secreted in the supernatant of C. fusca as a defence priming agent. This is the first report of the mechanism of innate immune activation by aquatic microalga Chlorella in higher plants.
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spelling pubmed-73181302020-06-29 d‐Lactic acid secreted by Chlorella fusca primes pattern‐triggered immunity against Pseudomonas syringae in Arabidopsis Lee, Sang‐Moo Kim, Seon‐Kyu Lee, Nakyeong Ahn, Chi‐Yong Ryu, Choong‐Min Plant J Original Articles Biological control agents including microbes and their products have been studied as sustainable crop protection strategies. Although aquatic microalgae have been recently introduced as a biological control agent, the underlying molecular mechanisms are largely unknown. The aim of the present study was to investigate the molecular mechanisms underlying biological control by microalga Chlorella fusca. Foliar application of C. fusca elicits induced resistance in Arabidopsis thaliana against Pseudomonas syringae pv. tomato DC3000 that activates plant immunity rather than direct antagonism. To understand the basis of C. fusca‐triggered induced resistance at the transcriptional level, we conducted RNA sequencing (RNA‐seq) analysis. RNA‐seq data showed that, upon pathogen inoculation, C. fusca treatment primed the expression of cysteine‐rich receptor‐like kinases, WRKY transcription factor genes, and salicylic acid and jasmonic acid signalling‐related genes. Intriguingly, the application of C. fusca primed pathogen‐associated molecular pattern ‐triggered immunity, characterized by reactive oxygen species burst and callose deposition, upon flagellin 22 treatment. The attempts to find C. fusca determinants allowed us to identify d‐lactic acid secreted in the supernatant of C. fusca as a defence priming agent. This is the first report of the mechanism of innate immune activation by aquatic microalga Chlorella in higher plants. John Wiley and Sons Inc. 2020-01-27 2020-05 /pmc/articles/PMC7318130/ /pubmed/31869481 http://dx.doi.org/10.1111/tpj.14661 Text en © 2019 The Authors. The Plant Journal published by Society for Experimental Biology and John Wiley & Sons Ltd 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 Original Articles
Lee, Sang‐Moo
Kim, Seon‐Kyu
Lee, Nakyeong
Ahn, Chi‐Yong
Ryu, Choong‐Min
d‐Lactic acid secreted by Chlorella fusca primes pattern‐triggered immunity against Pseudomonas syringae in Arabidopsis
title d‐Lactic acid secreted by Chlorella fusca primes pattern‐triggered immunity against Pseudomonas syringae in Arabidopsis
title_full d‐Lactic acid secreted by Chlorella fusca primes pattern‐triggered immunity against Pseudomonas syringae in Arabidopsis
title_fullStr d‐Lactic acid secreted by Chlorella fusca primes pattern‐triggered immunity against Pseudomonas syringae in Arabidopsis
title_full_unstemmed d‐Lactic acid secreted by Chlorella fusca primes pattern‐triggered immunity against Pseudomonas syringae in Arabidopsis
title_short d‐Lactic acid secreted by Chlorella fusca primes pattern‐triggered immunity against Pseudomonas syringae in Arabidopsis
title_sort d‐lactic acid secreted by chlorella fusca primes pattern‐triggered immunity against pseudomonas syringae in arabidopsis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318130/
https://www.ncbi.nlm.nih.gov/pubmed/31869481
http://dx.doi.org/10.1111/tpj.14661
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