Poster
Shu-Hua Hsu
Postdoctoral Researcher
Utrecht University
Utrecht, Utrecht, Netherlands
Max J.J Stassen
Utrecht University
Utrecht, Utrecht, Netherlands
Kevin Robe
IPSiM, University of Montpellier, CNRS, INRAE, Institut Agro
Montpellier, Languedoc-Roussillon, France
Esther Izquierdo
IPSiM, University of Montpellier, CNRS, INRAE, Institut Agro
Montpellier, Languedoc-Roussillon, France
Christian Dubos
IPSiM, University of Montpellier, CNRS, INRAE, Institut Agro
Montpellier, Languedoc-Roussillon, France
Corné M.J. Pieterse, PhD (he/him/his)
Professor Plant-Microbe Interactions
Utrecht University
Utrecht, Utrecht, Netherlands
Ioannis A. Stringlis
Agricultural University of Athens
Athens, Attiki, Greece
Induced systemic resistance (ISR) is a defense mechanism expressed in leaves upon root colonization by beneficial microbes. In the Arabidopsis-Pseudomonas simiae WCS417 (WCS417) model system, the root-specific transcription factor MYB72 is crucial in ISR onset. MYB72 together with downstream components F6’H1 and BGLU42 contribute to in the iron (Fe) deficiency response through the production of Fe-mobilizing coumarins. While coumarin-related genes are essential for ISR activation, the precise mechanisms remains unclear. To study this, we investigated the temporospatial transcriptomic and metabolic response related to coumarins in ISR-expressing Arabidopsis. RNA-seq analysis (1 to 7 days) showed that WCS417 activated a broad set of Fe deficiency- and coumarin biosynthesis-related genes, first in the roots and later in the shoots. Multispectral imaging showed differential coumarin distribution in roots of Fe-starved and WCS417-treated plants. Using liquid chromatography, we found that WCS417 treatment led to altered coumarin levels, with a transient peak observed in both roots and shoots. This suggests that systemic coumarin accumulation may play a role in ISR. ISR bioassays using the f6’h1 mutant and an F6’H1 overexpressing line further displyed that functional coumarin biosynthesis is essential for ISR establisment. Together, our findings reveal how the beneficial bacterium WCS417 reprograms plant-wide transcriptional activity to induce coumarin-dependent systemic resistance.