Abstract

Plant pathogenic fungi must be able to degrade host cell walls in order to penetrate and invade plant tissues. Among the plant cell wall degrading enzymes (PCWDEs) produced, xylanases are of special interest since its degradation target, xylan, is one of the main structural polysaccharides in plant cell walls. In the biotrophic fungus Ustilago maydis, attempts to characterize PCWDEs required for virulence have been unsuccessful, most likely due to functional redundancy. In previous high-throughput screening, we found one xylanase to be important for U. maydis infection. Here, we characterize the entire U. maydis endo-xylanase family, comprising two enzymes from the glycoside hydrolase (GH) 10 family, Xyn1 and Xyn2, one from GH11, Xyn11A, and one from GH43, Xyn3. We show that all endo-xylanases except Xyn3 are secreted and involved in infection in a non-redundant manner, suggesting different roles for each xylanase in this process. Taking a closer look inside the plant during the pathogenic process, we observed that all secreted xylanases were necessary for fungal proliferation. Finally, we found that at least Xyn11A accumulated in the apoplast of the infected plant after three days, highlighting the role of these enzymes as important secreted proteins during fungal proliferation inside plant tissues.

Highlights

  • Plant smut diseases, which mainly affect grasses, are caused by a variety of fungal species collectively known as smut fungi

  • As xylanases are found in the glycoside hydrolase (GH) 5, 7, 8, 10, 11, and 43 families, we performed an analysis for known proteins from those families in the U. maydis genome by examining the MycoCosm database [49]

  • We show that xylanases secreted by U. maydis GH10 and GH11 are involved in formation onsecreted the plantbysurface as well as during hyphae progression

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Summary

Introduction

Plant smut diseases, which mainly affect grasses, are caused by a variety of fungal species collectively known as smut fungi. These pathogens are able to produce large amounts of teliospores, mainly in host floral organs, affecting their reproduction [1]. The pathogenic cycle occurs when two sexually compatible strains come into contact on the maize plant surface and pheromones activate mutually compatible receptors. They form a conjugation tube and mate, developing a filamentous cell cycle-arrested dikaryon [5,6]. Hyphae subdivide as individual cells and undergo teliospore development

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