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Trichoderma asperellum empowers tomato plants and suppresses Fusarium oxysporum through priming responses

Plant-associated microbes play crucial roles in plant health and promote growth under stress. Tomato (Solanum lycopersicum) is one of the strategic crops grown throughout Egypt and is a widely grown vegetable worldwide. However, plant disease severely affects tomato production. The post-harvest dise...

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Autores principales: Sehim, Amira E., Hewedy, Omar A., Altammar, Khadijah A., Alhumaidi, Maryam S., Abd Elghaffar, Rasha Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043483/
https://www.ncbi.nlm.nih.gov/pubmed/36998401
http://dx.doi.org/10.3389/fmicb.2023.1140378
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author Sehim, Amira E.
Hewedy, Omar A.
Altammar, Khadijah A.
Alhumaidi, Maryam S.
Abd Elghaffar, Rasha Y.
author_facet Sehim, Amira E.
Hewedy, Omar A.
Altammar, Khadijah A.
Alhumaidi, Maryam S.
Abd Elghaffar, Rasha Y.
author_sort Sehim, Amira E.
collection PubMed
description Plant-associated microbes play crucial roles in plant health and promote growth under stress. Tomato (Solanum lycopersicum) is one of the strategic crops grown throughout Egypt and is a widely grown vegetable worldwide. However, plant disease severely affects tomato production. The post-harvest disease (Fusarium wilt disease) affects food security globally, especially in the tomato fields. Thus, an alternative effective and economical biological treatment to the disease was recently established using Trichoderma asperellum. However, the role of rhizosphere microbiota in the resistance of tomato plants against soil-borne Fusarium wilt disease (FWD) remains unclear. In the current study, a dual culture assay of T. asperellum against various phytopathogens (e.g., Fusarium oxysporum, F. solani, Alternaria alternata, Rhizoctonia solani, and F. graminerarum) was performed in vitro. Interestingly, T. asperellum exhibited the highest mycelial inhibition rate (53.24%) against F. oxysporum. In addition, 30% free cell filtrate of T. asperellum inhibited F. oxysporum by 59.39%. Various underlying mechanisms were studied to explore the antifungal activity against F. oxysporum, such as chitinase activity, analysis of bioactive compounds by gas chromatography–mass spectrometry (GC–MS), and assessment of fungal secondary metabolites against F. oxysporum mycotoxins in tomato fruits. Additionally, the plant growth-promoting traits of T. asperellum were studied (e.g., IAA production, Phosphate solubilization), and the impact on tomato seeds germination. Scanning electron microscopy, plant root sections, and confocal microscopy were used to show the mobility of the fungal endophyte activity to promote tomato root growth compared with untreated tomato root. T. asperellum enhanced the growth of tomato seeds and controlled the wilt disease caused by the phytopathogen F. oxysporum by enhancing the number of leaves as well as shoot and root length (cm) and fresh and dry weights (g). Furthermore, Trichoderma extract protects tomato fruits from post-harvest infection by F. oxysporum. Taking together, T. asperellum represents a safe and effective controlling agent against Fusarium infection of tomato plants.
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spelling pubmed-100434832023-03-29 Trichoderma asperellum empowers tomato plants and suppresses Fusarium oxysporum through priming responses Sehim, Amira E. Hewedy, Omar A. Altammar, Khadijah A. Alhumaidi, Maryam S. Abd Elghaffar, Rasha Y. Front Microbiol Microbiology Plant-associated microbes play crucial roles in plant health and promote growth under stress. Tomato (Solanum lycopersicum) is one of the strategic crops grown throughout Egypt and is a widely grown vegetable worldwide. However, plant disease severely affects tomato production. The post-harvest disease (Fusarium wilt disease) affects food security globally, especially in the tomato fields. Thus, an alternative effective and economical biological treatment to the disease was recently established using Trichoderma asperellum. However, the role of rhizosphere microbiota in the resistance of tomato plants against soil-borne Fusarium wilt disease (FWD) remains unclear. In the current study, a dual culture assay of T. asperellum against various phytopathogens (e.g., Fusarium oxysporum, F. solani, Alternaria alternata, Rhizoctonia solani, and F. graminerarum) was performed in vitro. Interestingly, T. asperellum exhibited the highest mycelial inhibition rate (53.24%) against F. oxysporum. In addition, 30% free cell filtrate of T. asperellum inhibited F. oxysporum by 59.39%. Various underlying mechanisms were studied to explore the antifungal activity against F. oxysporum, such as chitinase activity, analysis of bioactive compounds by gas chromatography–mass spectrometry (GC–MS), and assessment of fungal secondary metabolites against F. oxysporum mycotoxins in tomato fruits. Additionally, the plant growth-promoting traits of T. asperellum were studied (e.g., IAA production, Phosphate solubilization), and the impact on tomato seeds germination. Scanning electron microscopy, plant root sections, and confocal microscopy were used to show the mobility of the fungal endophyte activity to promote tomato root growth compared with untreated tomato root. T. asperellum enhanced the growth of tomato seeds and controlled the wilt disease caused by the phytopathogen F. oxysporum by enhancing the number of leaves as well as shoot and root length (cm) and fresh and dry weights (g). Furthermore, Trichoderma extract protects tomato fruits from post-harvest infection by F. oxysporum. Taking together, T. asperellum represents a safe and effective controlling agent against Fusarium infection of tomato plants. Frontiers Media S.A. 2023-03-14 /pmc/articles/PMC10043483/ /pubmed/36998401 http://dx.doi.org/10.3389/fmicb.2023.1140378 Text en Copyright © 2023 Sehim, Hewedy, Altammar, Alhumaidi and Abd Elghaffar. https://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 Microbiology
Sehim, Amira E.
Hewedy, Omar A.
Altammar, Khadijah A.
Alhumaidi, Maryam S.
Abd Elghaffar, Rasha Y.
Trichoderma asperellum empowers tomato plants and suppresses Fusarium oxysporum through priming responses
title Trichoderma asperellum empowers tomato plants and suppresses Fusarium oxysporum through priming responses
title_full Trichoderma asperellum empowers tomato plants and suppresses Fusarium oxysporum through priming responses
title_fullStr Trichoderma asperellum empowers tomato plants and suppresses Fusarium oxysporum through priming responses
title_full_unstemmed Trichoderma asperellum empowers tomato plants and suppresses Fusarium oxysporum through priming responses
title_short Trichoderma asperellum empowers tomato plants and suppresses Fusarium oxysporum through priming responses
title_sort trichoderma asperellum empowers tomato plants and suppresses fusarium oxysporum through priming responses
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043483/
https://www.ncbi.nlm.nih.gov/pubmed/36998401
http://dx.doi.org/10.3389/fmicb.2023.1140378
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