Abstract

Metabolic changes in sorghum seedlings in response to Paenibacillus alvei (NAS-6G6)-induced systemic resistance against Fusarium pseudograminearum crown rot were investigated by means of untargeted ultra-high performance liquid chromatography-high definition mass spectrometry (UHPLC-HDMS). Treatment of seedlings with the plant growth-promoting rhizobacterium P. alvei at a concentration of 1 × 108 colony forming units mL−1 prior to inoculation with F. pseudograminearum lowered crown rot disease severity significantly at the highest inoculum dose of 1 × 106 spores mL−1. Intracellular metabolites were subsequently methanol-extracted from treated and untreated sorghum roots, stems and leaves at 1, 4 and 7 days post inoculation (d.p.i.) with F. pseudograminearum. The extracts were analysed on an UHPLC-HDMS platform, and the data chemometrically processed to determine metabolic profiles and signatures related to priming and induced resistance. Significant treatment-related differences in primary and secondary metabolism post inoculation with F. pseudograminearum were observed between P. alvei-primed versus naïve S. bicolor seedlings. The differential metabolic reprogramming in primed plants comprised of a quicker and/or enhanced upregulation of amino acid-, phytohormone-, phenylpropanoid-, flavonoid- and lipid metabolites in response to inoculation with F. pseudograminearum.

Highlights

  • As an evolutionary adaptation to survive a sessile existence, in addition to pre-existing physical and chemical barriers, plants have developed the ability to actively protect themselves against environmental stress through the synthesis of complex and ever-changing mixtures of defence-related metabolites [1]

  • We investigated the protection offered by a Plant growth-promoting rhizobacteria (PGPR), P. alvei, in mitigating the disease susceptibility of sorghum seedlings towards F. pseudograminearum, the causative agent of crown rot disease

  • Priming S. bicolor seedlings with P. alvei NAS-6G6 resulted in the induction of systemic resistance against F. pseudograminearum

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Summary

Introduction

As an evolutionary adaptation to survive a sessile existence, in addition to pre-existing physical and chemical barriers, plants have developed the ability to actively protect themselves against environmental stress through the synthesis of complex and ever-changing mixtures of defence-related metabolites [1]. These metabolites can either be synthesised locally or systemically as part of systemic acquired resistance (SAR) [2,3]. It is hypothesised that in response to the negative ecological impact of SAR, evolutionary forces were directed towards the development of induced systemic resistance (ISR) [5]. During ISR, the plant is primed by beneficial microbes for an enhanced defensive response that only activates upon challenge with a stress, wasting no resources.

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