Xu Yuan, Liu Yuqing, Wang Yihan, Liu Yi, Zhu Guopeng
Sanya Nanfan Research Institute, Hainan University, Sanya 572025, China.
Key Laboratory for Quality Regulation of Tropical Horticultural Crops of Hainan Province, School of Tropical Agriculture and Forestry, Hainan University, Haikou 570228, China.
J Fungi (Basel). 2024 Dec 18;10(12):882. doi: 10.3390/jof10120882.
A pathogen strain responsible for sweet potato stem and foliage scab disease was isolated from sweet potato stems. Through a phylogenetic analysis based on the rDNA internal transcribed spacer (ITS) region, combined with morphological methods, the isolated strain was identified as To comprehensively analyze the pathogenicity of the isolated strain from a genetic perspective, the whole-genome sequencing of HD-1 was performed using both the PacBio and Illumina platforms. The genome of HD-1 is about 26.31 Mb long in 167 scaffolds, with a GC content of 50.81%, and 7898 protein-coding genes, 131 non-coding RNAs, and 1954 interspersed repetitive sequences were predicted. Functional annotation revealed that 408 genes encode virulence factors involved in plant disease (DFVF-Plant). Notably, twenty-eight of these virulence genes encode secretory carbohydrate-active enzymes (CAZymes), including two endo-1,4-β-xylanase genes and seven cutinase genes, which suggested that endo-1,4-β-xylanase and cutinase play a vital role in the pathogenicity of HD-1 within sweet potato. In total, twelve effectors were identified, including five LysM effectors and two CDIP effectors, suggesting that LysM and CDIP effectors play significant roles in the interaction between HD-1 and sweet potato. Additionally, our analysis of biosynthetic gene clusters (BGCs) showed that two gene clusters are involved in melanin and choline metabolism. This study enriches the genomic resources of and provides a theoretical foundation for future investigations into the pathogenic mechanisms of its infection in sweet potatoes, as well as potential targets for disease control.
从甘薯茎中分离出一种导致甘薯茎和叶疮痂病的病原菌菌株。通过基于核糖体DNA内部转录间隔区(ITS)区域的系统发育分析,并结合形态学方法,将分离出的菌株鉴定为。为了从基因角度全面分析分离菌株的致病性,使用PacBio和Illumina平台对HD-1进行了全基因组测序。HD-1的基因组约为26.31 Mb,分布在167个支架上,GC含量为50.81%,预测有7898个蛋白质编码基因、131个非编码RNA和1954个散布重复序列。功能注释显示,408个基因编码参与植物病害的毒力因子(DFVF-Plant)。值得注意的是,这些毒力基因中有28个编码分泌性碳水化合物活性酶(CAZymes),包括两个内切-1,4-β-木聚糖酶基因和七个角质酶基因,这表明内切-1,4-β-木聚糖酶和角质酶在HD-1对甘薯的致病性中起着至关重要的作用。总共鉴定出12个效应子,包括5个LysM效应子和2个CDIP效应子,这表明LysM和CDIP效应子在HD-1与甘薯的相互作用中发挥着重要作用。此外,我们对生物合成基因簇(BGCs)的分析表明,有两个基因簇参与黑色素和胆碱代谢。本研究丰富了的基因组资源,为今后研究其在甘薯中的感染致病机制以及疾病控制的潜在靶点提供了理论基础。