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Carbon and Nitrogen Sources Influence Parasitic Responsiveness in Trichoderma atroviride NI-1
Víctor Javier García-Sánchez1, Karina Lizbeth Sánchez-López1, Juana Jazmín Esquivel Méndez1
1Unit for Basic and Applied Microbiology, Faculty of Natural Sciences, Autonomous University of Queretaro, Queretaro 76140, Mexico.
Abstract:
Parasitic species of Trichoderma use hydrolytic enzymes to destroy the host cell wall. Preferent carbon and nitrogen sources suppress the expression of genes related to parasitism. Here, different nutrients were evaluated in the parasitic isolated NI-1, which was identified as Trichoderma atroviride. The genes cbh1 and chb2 (cellobiohydrolases), bgl3.1 (endoglucanase), and pra1 and prb1 (proteinases) were poorly expressed during the interaction between NI-1 and Phytophthora capsici on PDA. However, gene expression improved on minimal medium with preferent and alternative carbon sources. Dextrin and glucose stimulated higher transcript levels than cellulose, sucrose, and glycerol. Also, ammonium stimulated a stronger parasitic responsiveness than the alternative nitrogen sources. During interaction against different phytopathogens, NI-1 detects their host differentially from a distance due to the cbh1 and cbh2 genes being only induced by P. capsici. The pra1 and ech42 genes were induced before contact with Botrytis cinerea and Rhizoctonia solani, while when confronted with P. capsici they were stimulated until contact and overgrowth. The prb1 and bgl3.1 genes were induced before contact against the three-host assayed. Overall, T. atroviride prefers to parasitize and has the capacity to distinguish between an oomycete and a fungus, but nutrient quality regulates its parasitic responsiveness.
Insights
Trichoderma atroviride parasitism is regulated by nutrient availability. Preferential carbon and nitrogen sources enhance the expression of parasitic genes, enabling host discrimination between fungi and oomycetes.
Area of Science:
- * Mycology and Plant Pathology
- * Molecular Biology and Genetics
Background:
- * Parasitic fungi, such as Trichoderma species, utilize hydrolytic enzymes to degrade host cell walls.
- * The expression of parasitic genes in Trichoderma is known to be suppressed by preferred carbon and nitrogen sources.
- * Understanding nutrient regulation is crucial for harnessing Trichoderma's biocontrol potential.
Purpose of the Study:
- * To investigate the effect of different nutrient sources on the parasitic activity of Trichoderma atroviride isolate NI-1.
- * To analyze the expression patterns of key parasitic genes (cellobiohydrolases, endoglucanase, proteinases) under varying nutrient conditions.
- * To determine if T. atroviride can differentiate between fungal and oomycete hosts and how nutrient availability influences this interaction.
Main Methods:
- * Culturing of Trichoderma atroviride isolate NI-1 on Potato Dextrose Agar (PDA) and minimal media with various carbon and nitrogen sources.
- * Quantitative gene expression analysis of cbh1, cbh2, bgl3.1, pra1, prb1, and ech42 genes.
- * Co-culturing NI-1 with Phytophthora capsici, Botrytis cinerea, and Rhizoctonia solani to observe differential gene induction.
Main Results:
- * Gene expression for cellobiohydrolases (cbh1, cbh2), endoglucanase (bgl3.1), and proteinases (pra1, prb1) was low during interaction with Phytophthora capsici on PDA.
- * Dextrin and glucose as carbon sources, and ammonium as a nitrogen source, significantly enhanced the expression of parasitic genes in minimal media.
- * Specific genes (cbh1, cbh2) were uniquely induced by P. capsici, indicating host recognition from a distance. Other genes (pra1, ech42, prb1, bgl3.1) showed varied induction patterns before or upon contact with different pathogens.
Conclusions:
- * Nutrient availability, particularly carbon and nitrogen sources, significantly regulates the parasitic responsiveness of Trichoderma atroviride.
- * T. atroviride demonstrates the capacity to distinguish between oomycete (P. capsici) and fungal (B. cinerea, R. solani) hosts.
- * The study highlights the complex interplay between nutrient signaling and host recognition in Trichoderma-mediated parasitism.
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