Abstract

The present study investigated the transcriptomic and metabolomic changes elicited in tomato plants (Solanum lycopersicum cv. Micro-Tom) following treatments with the biocontrol agent Trichoderma harzianum strain M10 or its purified secondary metabolite harzianic acid (HA), in the presence or the absence of the soil-borne pathogen Rhizoctonia solani. Transcriptomic analysis allowed the identification of differentially expressed genes (DEGs) that play a pivotal role in resistance to biotic stress. Overall, the results support the ability of T. harzianum M10 to activate defense responses in infected tomato plants. An induction of hormone-mediated signaling was observed, as shown by the up-regulation of genes involved in the ethylene and jasmonate (ET/JA) and salicylic acid (SA)-mediated signaling pathways. Further, the protective action of T. harzianum on the host was revealed by the over-expression of genes able to detoxify cells from reactive oxygen species (ROS). On the other hand, HA treatment also stimulated tomato response to the pathogen by inducing the expression of several genes involved in defense response (including protease inhibitors, resistance proteins like CC-NBS-LRR) and hormone interplay. The accumulation of steroidal glycoalkaloids in the plant after treatments with either T. harzianum or HA, as determined by metabolomic analysis, confirmed the complexity of the plant response to beneficial microbes, demonstrating that these microorganisms are also capable of activating the chemical defenses.

Highlights

  • The complex network of interactions established by plants with the rhizosphere microbiota greatly affect crop health and fitness (Raaijmakers et al, 2009; Berendsen et al, 2012)

  • The biocontrol activity of T. harzianum M10 and harzianic acid (HA) against R. solani on tomato was evaluated as the percentage of infected plants observed at 7 different time points (Figure 1)

  • The 48 h postinoculum (HPI) time point was selected because it allowed the collection of a sufficient number of infected but still healthy plants for each experimental group, which is critical for obtaining a good quality RNA suitable for transcriptomic analysis

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Summary

Introduction

The complex network of interactions established by plants with the rhizosphere microbiota greatly affect crop health and fitness (Raaijmakers et al, 2009; Berendsen et al, 2012). Plant-microbe interactions include cases that may be detrimental, compromising plant growth and health, the establishment of a disease status is often counteracted by the presence of a beneficial soil microbial community that can hinder infection by disease pathogens (Matos et al, 2005; Walters et al, 2008) Mycoparasitic fungi such as Trichoderma and Gliocladium have antagonistic activity on many soilborne pathogens (including Verticillium, Sclerotinia, Rhizoctonia, Fusarium, Pythium) due to a variety of mechanisms, including: parasitism, competition for nutrients and space, antibiosis, and production of lytic enzymes, as well as the ability to trigger the induction of systemic resistance (ISR) (Harman et al, 2004b; Lorito et al, 2010; Doornbos et al, 2012; Hermosa et al, 2014; Amira et al, 2017; Nawrocka et al, 2018). With the implementation of Directive 2009/128/EC, the European Community promotes specific actions to support the establishment of sustainable agriculture through the reduced use of chemical pesticides in favor of alternative non-chemical products, and the promotion of integrated pest management (IPM)

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