Laboratory of Forest Pathology, Department of Plant Pathology, Universidade Federal de Viçosa, Minas Gerais State, Brazil; The New Zealand Institute for Plant and Food Research Limited, Auckland 1142, New Zealand.
Núcleo de Análise de Biomoléculas (NuBioMol), Centro de Ciências Biológicas, Universidade Federal de Viçosa, Minas Gerais State, Brazil.
Fungal Genet Biol. 2020 Apr;137:103332. doi: 10.1016/j.fgb.2019.103332. Epub 2020 Jan 8.
Ceratocystis fimbriata is an important plant pathogen known to cause Ceratocystis Wilt (CW), a prevalent fungal disease known to affect Eucalyptus spp. plantations in Brazil. To better understand the molecular mechanisms related to pathogenicity in eucalyptus, we generated a high-quality assembly and annotation of the Ce. fimbriata LPF1912 isolate (LPF1912) genome, as well as the first transcriptome of LPF1912 from 16 eucalyptus clones at three infection incubation periods (12, 18, and 24 h). The LPF1912 genome assembly contains 805 scaffolds, totaling 31.8 Mb, with 43% of the genome estimated to be coding sequence comprised of 7,390 protein-coding genes of which 626 (8.5%) were classified as secreted proteins, 120 ribosomal RNAs, and 532 transfer RNAs. Comparative genomic analysis among three eucalyptus fungal pathogens (Ce. fimbriata, Ce. eucalypticola, and Calonectria pseudoreteaudii), showed high similarity in the proteome (21.81%) and secretome (52.01%) of LPF1912 and Ce. eucalypticola. GO annotation of pathogenicity-related genes of LPF1912 and Ce. eucalypticola, revealed enrichment in cell wall degrading enzymes (CWDEs), and lipid/cutin metabolism for Ca. pseudoreteaudii. Additionally, a transcriptome analysis between resistant and susceptible eucalyptus clones to CW infection indicated that a majority (11) of LPF1912 differentially expressed genes had GO terms associated with enzymatic functions, such as the polygalacturonase gene family, confirming the crucial role of CWDEs for Ce. fimbriata pathogenicity. Finally, our genomic and transcriptomic analysis approach provides a better understanding of the mechanisms involved in Ce. fimbriata pathogenesis, as well as a framework for further studies.
棘壳炱菌是一种重要的植物病原菌,已知其可引起棘壳炱萎蔫病(Ceratocystis wilt,简称 CW),这是一种普遍存在的真菌病害,已知会影响巴西的桉树种植园。为了更好地了解桉树中与致病性相关的分子机制,我们生成了棘壳炱菌 LPF1912 分离株(LPF1912)基因组的高质量组装和注释,以及 LPF1912 来自 16 个桉树克隆在三个感染孵育期(12、18 和 24 小时)的首个转录组。LPF1912 基因组组装包含 805 个支架,总计 31.8 Mb,其中 43%的基因组估计为编码序列,由 7390 个蛋白质编码基因组成,其中 626 个(8.5%)被归类为分泌蛋白,120 个核糖体 RNA 和 532 个转移 RNA。对三种桉树真菌病原体(棘壳炱菌、拟小穴壳菌和拟茎点霉)的比较基因组分析表明,LPF1912 和拟小穴壳菌的蛋白质组(21.81%)和分泌组(52.01%)高度相似。LPF1912 和拟小穴壳菌与致病性相关基因的 GO 注释表明,细胞壁降解酶(CWDEs)和脂质/角鲨烯代谢富集。此外,对 CW 感染抗性和敏感性桉树克隆的转录组分析表明,LPF1912 的大多数(11)差异表达基因具有与酶功能相关的 GO 术语,如多聚半乳糖醛酸酶基因家族,证实了 CWDEs 对棘壳炱菌致病性的重要作用。最后,我们的基因组和转录组分析方法提供了对棘壳炱菌发病机制中涉及的机制的更好理解,以及进一步研究的框架。