Poster
SUBHANKAR BERA, PhD
Postdoc
Malopolska Center of Biotechnology, Jagiellonian University
Krakow, Malopolskie, Poland
Arpan Kumar Basak
Max Planck Institute for Plant Breeding Research
Köln, Nordrhein-Westfalen, Germany
Mohamadreza Mirzaei
Doctoral student
Malopolska Centre of Biotechnology, Jagiellonian University, Krakow, Poland.
Kraków, Malopolskie, Poland
Mariola Pislewska-Bednarek
Institute of Bioorganic Chemistry, Polish Academy of Sciences
Poznan, Wielkopolskie, Poland
Swati Sweta. Ghadei
Masters student
Department of Medical Biotechnology, Jagiellonian University, Krakow, Poland
Kraków, Malopolskie, Poland
Anna Piasecka
Institute of Bioorganic Chemistry, Polish Academy of Sciences
Poznań, Wielkopolskie, Poland
Rafał Ważny
Malopolska Centre of Biotechnology, Jagiellonian University, Krakow, Poland
Krakow, Malopolskie, Poland
Piotr Rozpądek
Malopolska Centre of Biotechnology, Jagiellonian University, Krakow, Poland
Krakow, Mazowieckie, Poland
Pawel Bednarek
Institute of Bioorganic Chemistry, Polish Academy of Sciences
Poznan, Wielkopolskie, Poland
Kenji Yamada
Malopolska Centre of Biotechnology, Jagiellonian University, Krakow, Poland
Kraków, Malopolskie, Poland
Brassicaceae plants have developed robust defence mechanisms through unique secondary metabolites, such as aliphatic glucosinolates (AG), indole glucosinolates (IG) and camalexin. Previous studies indicate that tryptophan-derived metabolites influence Arabidopsis thaliana root microbiota assembly. However, the precise interplay between the chemical defence and root-endophyte behaviour remains unclear. We explore how plants and endophytes change their behaviour in the absence of host defence chemicals using an endophyte Phomophsis columnaris and A. thaliana. We found that P. columnaris adversely affects the growth of cyp79b2,b3,myb28,29 quadruple mutant (qKO) that lacks AG, IG and camalexin. In this interaction, activation of PDF genes was observed in the host plants, whereas the fungi extensively activated carbohydrate-active and plant cell wall degrading enzyme genes. P. columnaris did not show an adverse effect on AG-deficient myb28,29 or IG-deficient myb34,51,122 mutants. The hyper-accumulation of camalexin was observed in myb28,29 and myb34,51,122 mutants, suggesting that the mutants prevent fungi overload by enhancing camalexin biosynthesis to compensate for the absence of other defence chemicals. These findings indicate that the host plants reprogram transcriptional profiling to overcome the defect of defensive metabolites, which is the combination of AG, IG and camalexin.