Colonisation of plant roots by selected beneficial Trichoderma fungi or Pseudomonas bacteria can result in the activation of a systemic defence response that is effective against a broad spectrum of pathogens. In Arabidopsis thaliana, induced systemic resistance (ISR) triggered by the rhizobacterial strain Pseudomonas fluorescens WCS417r is regulated by a jasmonic acid‐ and ethylene‐dependent defence signalling pathway. Jasmonic acid and ethylene also play a role in Trichoderma‐induced resistance. To further investigate the similarities between rhizobacteria‐ and Trichoderma‐induced resistance, we studied the response of Arabidopsis to root colonisation by Trichoderma asperellum T34. In many aspects T34‐ISR was similar to WCS417r‐ISR. First, colonisation of the roots by T34 rendered the leaves more resistant to the bacterial pathogen Pseudomonas syringae pv. tomato, the biotrophic oomycete Hyaloperonospora parasitica and the necrotrophic fungus Plectosphaerella cucumerina. Second, treatment of the roots with T34 primed the leaf tissue for enhanced jasmonic acid‐responsive gene expression and increased formation of callose‐containing papillae upon pathogen attack. Third, T34‐ISR was fully expressed in the salicylic acid impaired mutant sid2, but blocked in the defence regulatory mutant npr1. Finally, we show that the root‐specific transcription factor MYB72, which is essential in early signalling steps of WCS417r‐ISR, is also required for T34‐ISR. Together, these results indicate that the defence pathways triggered by beneficial Trichoderma and Pseudomonas spp. strains are highly similar and that MYB72 functions as an early node of convergence in the signalling pathways that are induced by these different beneficial microorganisms.
Trichoderma spp. is one of the most commonly used biological control agents against plant pathogens. This fungus produces changes in plant metabolism, thus increasing growth and enhancing resistance to biotic and abiotic stresses. However, its modes of action remain to be defined. In the first hours of interaction between cucumber plant roots and Trichoderma asperellum strain T34, salicylic and jasmonic acid levels and typical antipathogenic peroxidase activity increase in the cotyledons to different degrees depending on the applied concentration of the fungi. The use of 2-DE protein profiling and MS analysis allowed us to identify 28 proteins whose expression was affected in cotyledons after cucumber root colonization by Trichoderma applied at high concentrations: 17 were found to be up-regulated while 11 were down-regulated. Proteins involved in ROS scavenging, stress response, isoprenoid and ethylene biosynthesis, and in photosynthesis, photorespiration, and carbohydrate metabolism were differentially regulated by Trichoderma. The proteome changes found in this study help to give an understanding of how Trichoderma-treated plants become more resistant to pathogen attacks through the changes in expression of a set of defence-oriented proteins which can directly protect the plant or switch the metabolism to a defensive, nonassimilatory state.
Trichoderma asperellum strain T34 has been reported to control the disease caused by Fusarium oxysporum f.sp. lycopersici (Fol) on tomato plants. To study the importance of iron concentration in the growth media for the activity and competitiveness of T34 and the pathogen, we tested four iron concentrations in the nutrient solution [1, 10, 100, and 1000 microM provided as EDTA/Fe(III)] in a biological control experiment with T34 and Fol in tomato plants. The reduction of the Fusarium-infected shoot by T34 was only significant at 10 microM Fe. We hypothesized that Fe competition is one of the key factors in the biocontrol activity exerted by T34 against Fol, as an increase in Fe concentration over 10 microM would lead to the suppression of T34 siderophore synthesis and thus inhibition of Fe competition with Fol. T34 significantly reduced the populations of Fol at all the doses of Fe assayed. In contrast, Fol enhanced the populations of T34 at 1 and 10 microM Fe. Nevertheless, several plant physiological parameters like net CO(2) assimilation (A), stomatal conductance (g(s)), relative quantum efficiency of PSII (Phi(PSII)), and efficiency of excitation energy capture by open PSII reactive centers (Fv'/Fm') demonstrated the protection against Fol damage by treatment with T34 at 100 microM Fe. The first physiological parameter affected by the disease progression was g(s). Plant dry weight was decreased by Fe toxicity at 100 and 1,000 microM. T34-treated plants had significantly greater heights and dry weights than control plants at 1,000 microM Fe, even though T34 did not reduce the Fe content in leaves or stems. Furthermore, T34 enhanced plant height even at the optimal Fe concentration (10 microM) compared to control plants. In conclusion, T. asperellum strain T34 protected tomato plants from both biotic (Fusarium wilt disease) and abiotic stress [Fe(III) toxic effects].
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