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Genome comparison between the maize pathogens <i>Ustilago maydis</i> and <i>Sporisorium reilianum</i> revealed a large diversity region (19-1) containing nearly 30 effector gene candidates, whose deletion severely hampers virulence of both fungi. Dissection of the <i>S. reilianum</i> gene cluster resulted in the identification of one major contributor to virulence, <i>virulence-associated gene 2</i> (<i>vag2</i>; <i>sr10050</i>). Quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR) experiments revealed high expression of <i>vag2</i> during biotrophic growth of <i>S. reilianum</i>. Using the yeast secretion trap assay, we confirmed the existence of a functional signal peptide allowing protein secretion via the conventional secretory pathway. We identified the cytoplasmic maize chorismate mutase ZmCM2 by yeast two-hybrid screening as a possible interaction partner of Vag2. Interaction of the two proteins in planta was confirmed by bimolecular fluorescence complementation. qRT-PCR experiments revealed <i>vag2</i>-dependent downregulation of salicylic acid (SA)-induced genes, which correlated with higher SA levels in plant tissues colonized by Δ<i>vag2</i> deletion strains relative to <i>S. reilianum</i> wildtype strains. Metabolite analysis suggested rewiring of pathogen-induced SA biosynthesis by preferential conversion of the SA precursor chorismate into the aromatic amino acid precursor prephenate by ZmCM2 in the presence of Vag2. Possibly, the binding of Vag2 to ZmCM2 inhibits the back reaction of the ZmCM2-catalyzed interconversion of chorismate and prephenate, thus contributing to fungal virulence by lowering the plant SA-induced defenses.