Abstract

The hemibiotrophic plant pathogen Colletotrichum higginsianum infects Brassicaceae and in combination with Arabidopsis thaliana, represents an important model system to investigate various ecologically important fungal pathogens and their infection strategies. After penetration of plant cells by appressoria, C. higginsianum establishes large biotrophic primary hyphae in the first infected cell. Shortly thereafter, a switch to necrotrophic growth occurs leading to the invasion of neighboring cells by secondary hyphae. In a forward genetic screen for virulence mutants by insertional mutagenesis, we identified mutants that penetrate the plant but show a defect in the passage from biotrophy to necrotrophy. Genome sequencing and pulsed-field gel electrophoresis revealed that two mutants were lacking chromosome 11, encoding potential pathogenicity genes. We established a chromosome loss assay to verify that strains lacking this small chromosome abort infection during biotrophy, while their ability to grow on artificial media was not affected. C. higginsianum harbors a second small chromosome, which can be lost without effects on virulence or growth on agar plates. Furthermore, we found that chromosome 11 is required to suppress Arabidopsis thaliana plant defense mechanisms dependent on tryptophan derived secondary metabolites.

Highlights

  • IntroductionBiotrophic fungi like the rusts or powdery mildew fungi show a narrow host range and highly adapted genomes showing gene expansions of pathogenicity related genes while having a reduced repertoire of genes involved in primary and secondary metabolism

  • Pathogenic fungi employ different strategies for causing disease

  • Their ability to penetrate the A. thaliana host appeared normal, suggesting that they have some defect in switching from biotrophy to necrotrophic growth or fail to overcome host plant defense

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Summary

Introduction

Biotrophic fungi like the rusts or powdery mildew fungi show a narrow host range and highly adapted genomes showing gene expansions of pathogenicity related genes while having a reduced repertoire of genes involved in primary and secondary metabolism This specializes them to keep the infected host cells alive and suppress plant defense (Spanu et al, 2010; Duplessis et al, 2011; Raffaele and Kamoun, 2012). Extra- and intracellular effector proteins play a central role in regulating these interactions (Stergiopoulos and de Wit, 2009) Both effector-triggered susceptibility and effector-triggered immunity leave their marks in the genomes of pathogenic fungi which often show species-specific gene duplications and genome expansions involving effector functions required for virulence (Raffaele and Kamoun, 2012; Jones et al, 2016).

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