Molecular Traits Underlying the Growth Promotion and Metabolite Accumulation in Rheum palmatum Inoculated with Endophytic Trichoderma citrinoviride HT-1

• Published in: International journal of molecular sciences 2022-11, Vol.23 (21), p.13132
• Main Authors: Chen, Dawei, Shi, Wenjing, Wang, Yihan, Zhao, Jing, Zhang, Hui, Jia, Lingyun, Sun, Kun
• Format: Article
• Language: English
• Subjects: Accumulation; Biosynthesis; Endophytes; Fertilizers; Fungi; Gene expression; Genes; growth-promoting mechanisms; Herbal medicine; High performance liquid chromatography; Hypothesis testing; Inoculation; Medical research; Metabolism; Metabolites; Polymerase chain reaction; Rheum palmatum; RNA-seq; Secondary metabolites; Seedlings; Signal transduction; Spores; Trichoderma citrinoviride
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms232113132

Trichoderma spp. are an important plant-growth-promoting fungi. Trichoderma citrinoviride HT-1 was isolated from Rheum palmatum root, which has beneficial effects on growth and metabolite accumulation. However, the improvement mechanisms for growth and metabolite accumulation of T. citrinoviride HT-1 are unclear. In this study, RNA sequencing (RNA-seq) and high-performance liquid chromatography (HPLC) were used to measure the effect of different concentrations of conidial suspension of the HT-1 strain on the growth promotion and metabolite accumulation of R. palmatum seedlings. The results showed that the highest biomass and metabolites of R. palmatum seedlings were obtained through treatment with the HT-1 strain at a final spore concentration of 107 spores/mL. RNA sequencing indicated that 1662 genes were upregulated and 2155 genes were downregulated after inoculation with 107 spores/mL of the HT-1 strain. This strain induced significant upregulation of related genes in the phenylpropanoid biosynthesis pathway, plant hormone signal transduction pathway, biosynthesis of secondary metabolites pathway, and plant–pathogen interaction pathway in R. palmatum. The gene expression trends were revealed through quantitative real-time polymerase chain reaction (qRT-PCR) and were consistent with those determined by RNA-seq. Our results will help us to understand the growth-promoting mechanisms of the HT-1 strain on R. palmatum and provide a theoretical basis for the application of T. citrinoviride HT-1 as a biological fertilizer.