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Transcriptome Analysis of T. asperellum GDFS 1009 Revealed the Role of MUP1 Gene on the Methionine-Based Induction of Morphogenesis and Biological Control Activity

Trichoderma spp. are biological control agents extensively used against various plant pathogens. However, the key genes shared for the growth, development and biological activity are unclear. In this study, we explored the genes responsible for the growth and development of T. asperellum GDFS 1009 u...

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Autores principales: Karuppiah, Valliappan, Zhang, Cheng, Liu, Tong, Li, Yi, Chen, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963050/
https://www.ncbi.nlm.nih.gov/pubmed/36836329
http://dx.doi.org/10.3390/jof9020215
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author Karuppiah, Valliappan
Zhang, Cheng
Liu, Tong
Li, Yi
Chen, Jie
author_facet Karuppiah, Valliappan
Zhang, Cheng
Liu, Tong
Li, Yi
Chen, Jie
author_sort Karuppiah, Valliappan
collection PubMed
description Trichoderma spp. are biological control agents extensively used against various plant pathogens. However, the key genes shared for the growth, development and biological activity are unclear. In this study, we explored the genes responsible for the growth and development of T. asperellum GDFS 1009 under liquid-shaking culture compared to solid-surface culture. Transcriptome analysis revealed 2744 differentially expressed genes, and RT-qPCR validation showed that the high-affinity methionine permease MUP1 was the key gene for growth under different media. Deletion of the MUP1 inhibited the transport of amino acids, especially methionine, thereby inhibiting mycelial growth and sporulation, whereas inhibition could be mitigated by adding methionine metabolites such as SAM, spermidine and spermine. The MUP1 gene responsible for the methionine-dependent growth of T. asperellum was confirmed to be promoted through the PKA pathway but not the MAPK pathway. Furthermore, the MUP1 gene also increased the mycoparasitic activity of T. asperellum against Fusarium graminearum. Greenhouse experiments revealed that MUP1 strengthens the Trichoderma-induced crop growth promotion effect and SA-induced pathogen defense potential in maize. Our study highlights the effect of the MUP1 gene on growth and morphological differentiation and its importance for the agricultural application of Trichoderma against plant diseases.
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spelling pubmed-99630502023-02-26 Transcriptome Analysis of T. asperellum GDFS 1009 Revealed the Role of MUP1 Gene on the Methionine-Based Induction of Morphogenesis and Biological Control Activity Karuppiah, Valliappan Zhang, Cheng Liu, Tong Li, Yi Chen, Jie J Fungi (Basel) Article Trichoderma spp. are biological control agents extensively used against various plant pathogens. However, the key genes shared for the growth, development and biological activity are unclear. In this study, we explored the genes responsible for the growth and development of T. asperellum GDFS 1009 under liquid-shaking culture compared to solid-surface culture. Transcriptome analysis revealed 2744 differentially expressed genes, and RT-qPCR validation showed that the high-affinity methionine permease MUP1 was the key gene for growth under different media. Deletion of the MUP1 inhibited the transport of amino acids, especially methionine, thereby inhibiting mycelial growth and sporulation, whereas inhibition could be mitigated by adding methionine metabolites such as SAM, spermidine and spermine. The MUP1 gene responsible for the methionine-dependent growth of T. asperellum was confirmed to be promoted through the PKA pathway but not the MAPK pathway. Furthermore, the MUP1 gene also increased the mycoparasitic activity of T. asperellum against Fusarium graminearum. Greenhouse experiments revealed that MUP1 strengthens the Trichoderma-induced crop growth promotion effect and SA-induced pathogen defense potential in maize. Our study highlights the effect of the MUP1 gene on growth and morphological differentiation and its importance for the agricultural application of Trichoderma against plant diseases. MDPI 2023-02-06 /pmc/articles/PMC9963050/ /pubmed/36836329 http://dx.doi.org/10.3390/jof9020215 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Karuppiah, Valliappan
Zhang, Cheng
Liu, Tong
Li, Yi
Chen, Jie
Transcriptome Analysis of T. asperellum GDFS 1009 Revealed the Role of MUP1 Gene on the Methionine-Based Induction of Morphogenesis and Biological Control Activity
title Transcriptome Analysis of T. asperellum GDFS 1009 Revealed the Role of MUP1 Gene on the Methionine-Based Induction of Morphogenesis and Biological Control Activity
title_full Transcriptome Analysis of T. asperellum GDFS 1009 Revealed the Role of MUP1 Gene on the Methionine-Based Induction of Morphogenesis and Biological Control Activity
title_fullStr Transcriptome Analysis of T. asperellum GDFS 1009 Revealed the Role of MUP1 Gene on the Methionine-Based Induction of Morphogenesis and Biological Control Activity
title_full_unstemmed Transcriptome Analysis of T. asperellum GDFS 1009 Revealed the Role of MUP1 Gene on the Methionine-Based Induction of Morphogenesis and Biological Control Activity
title_short Transcriptome Analysis of T. asperellum GDFS 1009 Revealed the Role of MUP1 Gene on the Methionine-Based Induction of Morphogenesis and Biological Control Activity
title_sort transcriptome analysis of t. asperellum gdfs 1009 revealed the role of mup1 gene on the methionine-based induction of morphogenesis and biological control activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963050/
https://www.ncbi.nlm.nih.gov/pubmed/36836329
http://dx.doi.org/10.3390/jof9020215
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