Constitutive plant defence relies on highly bioactive compounds. One such compound is polygodial, a terpenoid with extreme antifeedant and antimicrobial activities1, found in remarkably high quantities in the native Australian pepper Tasmannia lanceolata (Poir.), which gives this plant its iconic flavour and high market value. Generally effective against pests and pathogens, polygodial is also toxic to the plant and to the endophytic microbes known to enhance growth. Native pepper prevents unwanted toxic effects by storing polygodial into specialised oil cells called idiocytes (or idioblasts). Disruption of idiocytes by feeding insects or pathogenic fungi triggers the release of polygodial, constituting a general defence mechanism. However, we have limited understanding of how polygodial is synthesised and stored, and how adaptive it is to the plant-microbe relationship. This can now be discovered by combining the experimental resources established by the team and the cellular resolution afforded by spatial RNA sequencing.

After sequncing it genome as part of the Genome for Australian Plant initiative aims to explore a new paradigm in plant defence, shifting from the resource allocation theory between growth and defence towards the novel hypothesis of a trade-off between toxification against pathogens and facilitation of beneficial endophytes. Native pepper is an illuminating model to test this hypothesis: polygodial, as the single most important defence molecule accounting for 30% of the plant’s essential oil, is highly tractable. Within the species, polygodial content greatly varies among Tasmanian clones, highlighting substantial genetic differences5. Our team has shown that clones differ in susceptibility to the pathogenic fungus Phytophthora cinnamomi6. However, this fungus infects root tissues, where we found polygodial concentration is very low and where we hypothesise endophytes are essential. At the individual plant level, this long-lived evergreen shrub allows probing of different organs and developmental stages non-destructively over the year. After assembling its reference genome, we are now analysing multi-tissue, multi-stage transcriptomes to get a molecular understanding of the mechanisms involved in the non-host specific defence.