Among abiotic stresses, drought is undoubtedly one of the most severe environmental factors for a wide range of major crops, leading to considerable yield and economic losses. The adverse effects in crop yield reflect the result of a series of morphological and physiological changes but also changes in signaling pathways, transcriptional and post-transcriptional regulation of stress-responsive genes, and metabolic adaptations. Despite the exhausting studies elucidating plants’ metabolic response to drought, there is a knowledge gap in the biochemical mechanisms governing drought tolerance in lentil (Lens culinaris Medik.). The present study aimed to determine the fluctuations of the metabolite profiles of lentil genotypes with contrasting drought tolerance to discover possible biomarkers for screening tolerant genotypes at early growth stages. Lentil seedlings were subjected to osmotic drought stress, induced by polyethylene glycol, at two stress levels (2.5% and 5.0% PEG-6000) for a period of 20 days, while untreated plants were also included as controls. GC/ΕΙ/MS-mediated metabolic profiling was employed to monitor changes in response to osmotic drought stress. The data was subjected to OPLS-DA and OPLS-HCA for the discrimination between treatments and the discovery of trends and corresponding biomarkers. In total, the analysis yielded 150 metabolite features with highly reproducible patterns, of which the vast majority belonged to carbohydrates, carboxylic acids, and amino acids. Overall, findings highlight the differential accumulation of a series of compounds, and more importantly, the variable accumulation of certain metabolites, namely D-fructose, α,α-trehalose, myo-inositol, and L-tryptophan, in the contrasting genotypes, indicating that the adaptive metabolic responses to osmotic drought stress operate under strong genotypic dependency in lentil. Research findings provide insights into various aspects of lentil’s metabolism under drought and further offer the possibility of applying such knowledge towards effectively screening for drought-tolerant lentil germplasm at early growth stages.
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