Austropuccinia psidii, originating in South America, is a globally invasive plant pathogen causing rust disease on Myrtaceae. Several biotypes are recognized with the most widely distributed pandemic strain spreading throughout the Asia-Pacific and Oceania regions within the last decade. Austropuccinia psidii has a broad host range (currently 480 myrtaceous species), making it a particularly dangerous plant pathogen. In the nine years since the pandemic biotype was first found in Australia in 2010, the pathogen has caused the near extinction of at least three species, the decline of at least one keystone species, and negatively affected commercial production of several Myrtaceae. To enable molecular and genomic studies into A. psidii pathogenicity, we assembled a highly contiguous genome for the pandemic biotype based on PacBio sequence data and scaffolding with Hi-C technology. With an estimated haploid genome size of just over 1 Gbp, it is the largest assembled fungal genome to date. We found the A. psidii genome to have a lower GC content (33.8 %), greatly expanded telomeric and intergenic regions and more repetitive regions (> 90 %) compared to other genomes of species in the Pucciniales, however numbers of predicted coding regions (18,875) are comparable. Most of the increase in genome size is caused by a recent expansion of transposable elements belonging to the Gypsy superfamily. Post-inoculation mRNA sequence capture from a susceptible host provides expression evidence for 10,613 predicted coding genes, including 210 of the 367 putative effectors. The completeness of the genome provides a greatly needed resource for strategic approaches to combat disease spread.3