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Enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus

Roots of most terrestrial plants form symbiotic associations (mycorrhiza) with soil- borne arbuscular mycorrhizal fungi (AMF). Many studies show that mycorrhizal colonization enhances plant resistance against pathogenic fungi. However, the mechanism of mycorrhiza-induced disease resistance remains e...

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Autores principales: Song, Yuanyuan, Chen, Dongmei, Lu, Kai, Sun, Zhongxiang, Zeng, Rensen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585261/
https://www.ncbi.nlm.nih.gov/pubmed/26442091
http://dx.doi.org/10.3389/fpls.2015.00786
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author Song, Yuanyuan
Chen, Dongmei
Lu, Kai
Sun, Zhongxiang
Zeng, Rensen
author_facet Song, Yuanyuan
Chen, Dongmei
Lu, Kai
Sun, Zhongxiang
Zeng, Rensen
author_sort Song, Yuanyuan
collection PubMed
description Roots of most terrestrial plants form symbiotic associations (mycorrhiza) with soil- borne arbuscular mycorrhizal fungi (AMF). Many studies show that mycorrhizal colonization enhances plant resistance against pathogenic fungi. However, the mechanism of mycorrhiza-induced disease resistance remains equivocal. In this study, we found that mycorrhizal inoculation with AMF Funneliformis mosseae significantly alleviated tomato (Solanum lycopersicum Mill.) early blight disease caused by Alternaria solani Sorauer. AMF pre-inoculation led to significant increases in activities of β-1,3-glucanase, chitinase, phenylalanine ammonia-lyase (PAL) and lipoxygenase (LOX) in tomato leaves upon pathogen inoculation. Mycorrhizal inoculation alone did not influence the transcripts of most genes tested. However, pathogen attack on AMF-inoculated plants provoked strong defense responses of three genes encoding pathogenesis-related proteins, PR1, PR2, and PR3, as well as defense-related genes LOX, AOC, and PAL, in tomato leaves. The induction of defense responses in AMF pre-inoculated plants was much higher and more rapid than that in un-inoculated plants in present of pathogen infection. Three tomato genotypes: a Castlemart wild-type (WT) plant, a jasmonate (JA) biosynthesis mutant (spr2), and a prosystemin-overexpressing 35S::PS plant were used to examine the role of the JA signaling pathway in AMF-primed disease defense. Pathogen infection on mycorrhizal 35S::PS plants led to higher induction of defense-related genes and enzymes relative to WT plants. However, pathogen infection did not induce these genes and enzymes in mycorrhizal spr2 mutant plants. Bioassays showed that 35S::PS plants were more resistant and spr2 plants were more susceptible to early blight compared with WT plants. Our finding indicates that mycorrhizal colonization enhances tomato resistance to early blight by priming systemic defense response, and the JA signaling pathway is essential for mycorrhiza-primed disease resistance.
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spelling pubmed-45852612015-10-05 Enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus Song, Yuanyuan Chen, Dongmei Lu, Kai Sun, Zhongxiang Zeng, Rensen Front Plant Sci Plant Science Roots of most terrestrial plants form symbiotic associations (mycorrhiza) with soil- borne arbuscular mycorrhizal fungi (AMF). Many studies show that mycorrhizal colonization enhances plant resistance against pathogenic fungi. However, the mechanism of mycorrhiza-induced disease resistance remains equivocal. In this study, we found that mycorrhizal inoculation with AMF Funneliformis mosseae significantly alleviated tomato (Solanum lycopersicum Mill.) early blight disease caused by Alternaria solani Sorauer. AMF pre-inoculation led to significant increases in activities of β-1,3-glucanase, chitinase, phenylalanine ammonia-lyase (PAL) and lipoxygenase (LOX) in tomato leaves upon pathogen inoculation. Mycorrhizal inoculation alone did not influence the transcripts of most genes tested. However, pathogen attack on AMF-inoculated plants provoked strong defense responses of three genes encoding pathogenesis-related proteins, PR1, PR2, and PR3, as well as defense-related genes LOX, AOC, and PAL, in tomato leaves. The induction of defense responses in AMF pre-inoculated plants was much higher and more rapid than that in un-inoculated plants in present of pathogen infection. Three tomato genotypes: a Castlemart wild-type (WT) plant, a jasmonate (JA) biosynthesis mutant (spr2), and a prosystemin-overexpressing 35S::PS plant were used to examine the role of the JA signaling pathway in AMF-primed disease defense. Pathogen infection on mycorrhizal 35S::PS plants led to higher induction of defense-related genes and enzymes relative to WT plants. However, pathogen infection did not induce these genes and enzymes in mycorrhizal spr2 mutant plants. Bioassays showed that 35S::PS plants were more resistant and spr2 plants were more susceptible to early blight compared with WT plants. Our finding indicates that mycorrhizal colonization enhances tomato resistance to early blight by priming systemic defense response, and the JA signaling pathway is essential for mycorrhiza-primed disease resistance. Frontiers Media S.A. 2015-09-28 /pmc/articles/PMC4585261/ /pubmed/26442091 http://dx.doi.org/10.3389/fpls.2015.00786 Text en Copyright © 2015 Song, Chen, Lu, Sun and Zeng. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Song, Yuanyuan
Chen, Dongmei
Lu, Kai
Sun, Zhongxiang
Zeng, Rensen
Enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus
title Enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus
title_full Enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus
title_fullStr Enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus
title_full_unstemmed Enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus
title_short Enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus
title_sort enhanced tomato disease resistance primed by arbuscular mycorrhizal fungus
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585261/
https://www.ncbi.nlm.nih.gov/pubmed/26442091
http://dx.doi.org/10.3389/fpls.2015.00786
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