4.6 Article

Comparative genomic and transcriptomic analyses reveal the hemibiotrophic stage shift of Colletotrichum fungi

Journal

NEW PHYTOLOGIST
Volume 197, Issue 4, Pages 1236-1249

Publisher

WILEY
DOI: 10.1111/nph.12085

Keywords

cell wall-degrading enzymes; Colletotrichum; effectors; genome; hemibiotrophy; plant pathogenomics; protease; secondary metabolite

Categories

Funding

  1. Programme for Promotion of Basic and Applied Researches for Innovations in Bio-oriented Industry
  2. KAKENHI [24228008, 21380031]
  3. Kyoto Prefectural University
  4. Grants-in-Aid for Scientific Research [21380031] Funding Source: KAKEN

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Hemibiotrophic fungal plant pathogens represent a group of agronomically significant disease-causing agents that grow first on living tissue and then cause host death in later, necrotrophic growth. Among these, Colletotrichum spp. are devastating pathogens of many crops. Identifying expanded classes of genes in the genomes of phytopathogenic Colletotrichum, especially those associated with specific stages of hemibiotrophy, can provide insights on how these pathogens infect a large number of hosts. The genomes of Colletotrichum orbiculare, which infects cucurbits and Nicotiana benthamiana, and C.gloeosporioides, which infects a wide range of crops, were sequenced and analyzed, focusing on features with potential roles in pathogenicity. Regulation of C.orbiculare gene expression was investigated during infection of N.benthamiana using a custom microarray. Genes expanded in both genomes compared to other fungi included sequences encoding small, secreted proteins (SSPs), secondary metabolite synthesis genes, proteases and carbohydrate-degrading enzymes. Many SSP and secondary metabolite synthesis genes were upregulated during initial stages of host colonization, whereas the necrotrophic stage of growth is characterized by upregulation of sequences encoding degradative enzymes. Hemibiotrophy in C.orbiculare is characterized by distinct stage-specific gene expression profiles of expanded classes of potential pathogenicity genes.

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