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Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis
Authors:Kämper Jörg  Kahmann Regine  Bölker Michael  Ma Li-Jun  Brefort Thomas  Saville Barry J  Banuett Flora  Kronstad James W  Gold Scott E  Müller Olaf  Perlin Michael H  Wösten Han A B  de Vries Ronald  Ruiz-Herrera José  Reynaga-Peña Cristina G  Snetselaar Karen  McCann Michael  Pérez-Martín José  Feldbrügge Michael  Basse Christoph W  Steinberg Gero  Ibeas Jose I  Holloman William  Guzman Plinio  Farman Mark  Stajich Jason E  Sentandreu Rafael  González-Prieto Juan M  Kennell John C  Molina Lazaro  Schirawski Jan  Mendoza-Mendoza Artemio  Greilinger Doris  Münch Karin  Rössel Nicole  Scherer Mario  Vranes Miroslav
Institution:Department of Organismic Interactions, Max Planck Institute for Terrestrial Microbiology, Karl-von-Frisch Strasse, D-35043 Marburg, Germany. kahmann@mpi-marburg.mpg.de
Abstract:Ustilago maydis is a ubiquitous pathogen of maize and a well-established model organism for the study of plant-microbe interactions. This basidiomycete fungus does not use aggressive virulence strategies to kill its host. U. maydis belongs to the group of biotrophic parasites (the smuts) that depend on living tissue for proliferation and development. Here we report the genome sequence for a member of this economically important group of biotrophic fungi. The 20.5-million-base U. maydis genome assembly contains 6,902 predicted protein-encoding genes and lacks pathogenicity signatures found in the genomes of aggressive pathogenic fungi, for example a battery of cell-wall-degrading enzymes. However, we detected unexpected genomic features responsible for the pathogenicity of this organism. Specifically, we found 12 clusters of genes encoding small secreted proteins with unknown function. A significant fraction of these genes exists in small gene families. Expression analysis showed that most of the genes contained in these clusters are regulated together and induced in infected tissue. Deletion of individual clusters altered the virulence of U. maydis in five cases, ranging from a complete lack of symptoms to hypervirulence. Despite years of research into the mechanism of pathogenicity in U. maydis, no 'true' virulence factors had been previously identified. Thus, the discovery of the secreted protein gene clusters and the functional demonstration of their decisive role in the infection process illuminate previously unknown mechanisms of pathogenicity operating in biotrophic fungi. Genomic analysis is, similarly, likely to open up new avenues for the discovery of virulence determinants in other pathogens.
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