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Pochonia chlamydosporia Induces Plant-Dependent Systemic Resistance to Meloidogyne incognita

Meloidogyne spp. are the most damaging plant parasitic nematodes for horticultural crops worldwide. Pochonia chlamydosporia is a fungal egg parasite of root-knot and cyst nematodes able to colonize the roots of several plant species and shown to induce plant defense mechanisms in fungal-plant intera...

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Autores principales: Ghahremani, Zahra, Escudero, Nuria, Saus, Ester, Gabaldón, Toni, Sorribas, F. Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700505/
https://www.ncbi.nlm.nih.gov/pubmed/31456811
http://dx.doi.org/10.3389/fpls.2019.00945
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author Ghahremani, Zahra
Escudero, Nuria
Saus, Ester
Gabaldón, Toni
Sorribas, F. Javier
author_facet Ghahremani, Zahra
Escudero, Nuria
Saus, Ester
Gabaldón, Toni
Sorribas, F. Javier
author_sort Ghahremani, Zahra
collection PubMed
description Meloidogyne spp. are the most damaging plant parasitic nematodes for horticultural crops worldwide. Pochonia chlamydosporia is a fungal egg parasite of root-knot and cyst nematodes able to colonize the roots of several plant species and shown to induce plant defense mechanisms in fungal-plant interaction studies, and local resistance in fungal-nematode-plant interactions. This work demonstrates the differential ability of two out of five P. chlamydosporia isolates, M10.43.21 and M10.55.6, to induce systemic resistance against M. incognita in tomato but not in cucumber in split-root experiments. The M10.43.21 isolate reduced infection (32–43%), reproduction (44–59%), and female fecundity (14.7–27.6%), while the isolate M10.55.6 only reduced consistently nematode reproduction (35–47.5%) in the two experiments carried out. The isolate M10.43.21 induced the expression of the salicylic acid pathway (PR-1 gene) in tomato roots 7 days after being inoculated with the fungal isolate and just after nematode inoculation, and at 7 and 42 days after nematode inoculation too. The jasmonate signaling pathway (Lox D gene) was also upregulated at 7 days after nematode inoculation. Thus, some isolates of P. chlamydosporia can induce systemic resistance against root-knot nematodes but this is plant species dependent.
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spelling pubmed-67005052019-08-27 Pochonia chlamydosporia Induces Plant-Dependent Systemic Resistance to Meloidogyne incognita Ghahremani, Zahra Escudero, Nuria Saus, Ester Gabaldón, Toni Sorribas, F. Javier Front Plant Sci Plant Science Meloidogyne spp. are the most damaging plant parasitic nematodes for horticultural crops worldwide. Pochonia chlamydosporia is a fungal egg parasite of root-knot and cyst nematodes able to colonize the roots of several plant species and shown to induce plant defense mechanisms in fungal-plant interaction studies, and local resistance in fungal-nematode-plant interactions. This work demonstrates the differential ability of two out of five P. chlamydosporia isolates, M10.43.21 and M10.55.6, to induce systemic resistance against M. incognita in tomato but not in cucumber in split-root experiments. The M10.43.21 isolate reduced infection (32–43%), reproduction (44–59%), and female fecundity (14.7–27.6%), while the isolate M10.55.6 only reduced consistently nematode reproduction (35–47.5%) in the two experiments carried out. The isolate M10.43.21 induced the expression of the salicylic acid pathway (PR-1 gene) in tomato roots 7 days after being inoculated with the fungal isolate and just after nematode inoculation, and at 7 and 42 days after nematode inoculation too. The jasmonate signaling pathway (Lox D gene) was also upregulated at 7 days after nematode inoculation. Thus, some isolates of P. chlamydosporia can induce systemic resistance against root-knot nematodes but this is plant species dependent. Frontiers Media S.A. 2019-08-13 /pmc/articles/PMC6700505/ /pubmed/31456811 http://dx.doi.org/10.3389/fpls.2019.00945 Text en Copyright © 2019 Ghahremani, Escudero, Saus, Gabaldón and Sorribas. 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) and the copyright owner(s) 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
Ghahremani, Zahra
Escudero, Nuria
Saus, Ester
Gabaldón, Toni
Sorribas, F. Javier
Pochonia chlamydosporia Induces Plant-Dependent Systemic Resistance to Meloidogyne incognita
title Pochonia chlamydosporia Induces Plant-Dependent Systemic Resistance to Meloidogyne incognita
title_full Pochonia chlamydosporia Induces Plant-Dependent Systemic Resistance to Meloidogyne incognita
title_fullStr Pochonia chlamydosporia Induces Plant-Dependent Systemic Resistance to Meloidogyne incognita
title_full_unstemmed Pochonia chlamydosporia Induces Plant-Dependent Systemic Resistance to Meloidogyne incognita
title_short Pochonia chlamydosporia Induces Plant-Dependent Systemic Resistance to Meloidogyne incognita
title_sort pochonia chlamydosporia induces plant-dependent systemic resistance to meloidogyne incognita
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700505/
https://www.ncbi.nlm.nih.gov/pubmed/31456811
http://dx.doi.org/10.3389/fpls.2019.00945
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