Fusarium wilt disease is of global significance, affecting over 100 plant species. Those of highest agricultural importance in Australia are cotton, banana, tomato, legumes and cucurbits. The disease is caused by members of the F. oxysporum species complex, with pathogenic members causatively defined by their pathogenicity or lineage specific chromosomes, which are encoded with high levels of plasticity.
Using model plant systems (Arabidopsis thaliana, Medicago truncatula) coupled with powerful genetic, genomic, transcriptomic, and bioinformatics approaches, the team has made step changes in our understanding of the molecular dialogue that takes place between pathogen and host. The knowledge gained has been used to remove plant susceptibility genes, to track pathogen evolution and identify weaknesses in the pathogen to be exploited in resistance breeding.
Fusariam head blight and crown rot
Fusarium crown rot is a major disease in wheat and barley in Australia. It is an infection of the stem base of cereal plants which causes yield loss and is particularly prevalent in dry seasons. The primary causal agent in Australia is Fusarium pseudograminearum. Resistance or tolerance to this disease is quantitative with no absolute immunity available in current wheat cultivars. Fusarium head blight is a sporadic disease in parts of Australia, but is globally one of the most important disease of wheat and barley. It is primarily caused by Fusarium graminearum but F. pseudograminearum is also know to incite the disease in Australia. The team based in the Brisbane laboratories investigates the interaction from multiple angles including:
• The identification and mapping of resistance loci for germplasm improvement,
• The understanding the molecular mechanisms of the host response to infection and
• Mechanisms of pathogen virulence.
On the pathogen side of the interaction, we use genomic technologies to dissect mechanisms of virulence. Functional studies are undertaken with a particular focus on regulation and biosynthesis of toxins, biosynthesis of plant hormone mimics and mechanisms of degradation of host produced antimicrobial compounds. These fungi are easily cultured in the lab, have small genomes and can be transformed to create mutants or fluorescently tagged isolates. These organisms’ genomes are also very compact with related genes, such as those for toxin biosynthesis, present in gene clusters.