The pathogenic mechanisms of Tilletia horrida as revealed by comparative and functional genomics.
Aijun WangLinxiu PangNa WangPeng AiDesuo YinShuangcheng LiQiming DengJun ZhuYueyang LiangJianqing ZhuPing LiAiping ZhengPublished in: Scientific reports (2018)
Tilletia horrida is a soil-borne, mononucleate basidiomycete fungus with a biotrophic lifestyle that causes rice kernel smut, a disease that is distributed throughout hybrid rice growing areas worldwide. Here we report on the high-quality genome sequence of T. horrida; it is composed of 23.2 Mb that encode 7,729 predicted genes and 6,973 genes supported by RNA-seq. The genome contains few repetitive elements that account for 8.45% of the total. Evolutionarily, T. horrida lies close to the Ustilago fungi, suggesting grass species as potential hosts, but co-linearity was not observed between T. horrida and the barley smut Ustilago hordei. Genes and functions relevant to pathogenicity were presumed. T. horrida possesses a smaller set of carbohydrate-active enzymes and secondary metabolites, which probably reflect the specific characteristics of its infection and biotrophic lifestyle. Genes that encode secreted proteins and enzymes of secondary metabolism, and genes that are represented in the pathogen-host interaction gene database genes, are highly expressed during early infection; this is consistent with their potential roles in pathogenicity. Furthermore, among the 131 candidate pathogen effectors identified according to their expression patterns and functionality, we validated two that trigger leaf cell death in Nicotiana benthamiana. In summary, we have revealed new molecular mechanisms involved in the evolution, biotrophy, and pathogenesis of T. horrida.
Keyphrases
- genome wide
- genome wide identification
- rna seq
- cell death
- bioinformatics analysis
- single cell
- genome wide analysis
- cardiovascular disease
- dna methylation
- physical activity
- type diabetes
- poor prognosis
- transcription factor
- gene expression
- emergency department
- copy number
- cystic fibrosis
- high frequency
- cell proliferation
- climate change
- pseudomonas aeruginosa
- binding protein
- escherichia coli
- signaling pathway