Unveiling the Core Effector Proteins of Oil Palm Pathogen Ganoderma boninense via Pan-Secretome Analysis

• Published in: Journal of fungi (Basel) Vol. 8; no. 8; p. 793
• Main Authors: Khairi, Mohamad Hazwan Fikri, Nor Muhammad, Nor Azlan, Bunawan, Hamidun, Abdul Murad, Abdul Munir, Ramzi, Ahmad Bazli
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 29-07-2022; MDPI
• Subjects: Adaptation; basal stem rot; effector proteins; Enzymes; Fungi; Ganoderma boninense; Genes; genome architecture; genome-wide analysis; Genomes; Infections; Lignin; pan-secretome; Pathogenesis; Pathogenicity; Pathogens; Proteins; Secretome; Stem rot; Virulence; Malaysia; Indonesia
• ISSN: 2309-608X; 2309-608X
• DOI: 10.3390/jof8080793

Ganoderma boninense is the major causal agent of basal stem rot (BSR) disease in oil palm, causing the progressive rot of the basal part of the stem. Despite its prominence, the key pathogenicity determinants for the aggressive nature of hemibiotrophic infection remain unknown. In this study, genome sequencing and the annotation of G. boninense T10 were carried out using the Illumina sequencing platform, and comparative genome analysis was performed with previously reported G. boninense strains (NJ3 and G3). The pan-secretome of G. boninense was constructed and comprised 937 core orthogroups, 243 accessory orthogroups, and 84 strain-specific orthogroups. In total, 320 core orthogroups were enriched with candidate effector proteins (CEPs) that could be classified as carbohydrate-active enzymes, hydrolases, and non-catalytic proteins. Differential expression analysis revealed an upregulation of five CEP genes that was linked to the suppression of PTI signaling cascade, while the downregulation of four CEP genes was linked to the inhibition of PTI by preventing host defense elicitation. Genome architecture analysis revealed the one-speed architecture of the G. boninense genome and the lack of preferential association of CEP genes to transposable elements. The findings obtained from this study aid in the characterization of pathogenicity determinants and molecular biomarkers of BSR disease.