Guangdong Province Key Laboratory of Microbial Signals and Disease Control, College of Plant Protection, South China Agricultural University, Guangzhou 510642, China.
College of Life Sciences, Zhejiang University, Hangzhou 310030, China.
Int J Mol Sci. 2023 Feb 22;24(5):4376. doi: 10.3390/ijms24054376.
Anthracnose disease of cruciferous plants caused by is a serious fungal disease that affects cruciferous crops such as Chinese cabbage, Chinese flowering cabbage, broccoli, mustard plant, as well as the model plant . Dual transcriptome analysis is commonly used to identify the potential mechanisms of interaction between host and pathogen. In order to identify differentially expressed genes (DEGs) in both the pathogen and host, the conidia of wild-type (ChWT) and mutant (Δ) strains were inoculated onto leaves of , and the infected leaves of at 8, 22, 40, and 60 h post-inoculation (hpi) were subjected to dual RNA-seq analysis. The results showed that comparison of gene expression between the 'ChWT' and 'Δ' samples detected 900 DEGs (306 upregulated and 594 down-regulated) at 8 hpi, 692 DEGs (283 upregulated and 409 down-regulated) at 22 hpi, 496 DEGs (220 upregulated and 276 down-regulated) at 40 hpi, and 3159 DEGs (1544 upregulated and 1615 down-regulated) at 60 hpi. GO and KEGG analyses found that the DEGs were mainly involved in fungal development, biosynthesis of secondary metabolites, plant-fungal interactions, and phytohormone signaling. The regulatory network of key genes annotated in the Pathogen-Host Interactions database (PHI-base) and Plant Resistance Genes database (PRGdb), as well as a number of key genes highly correlated with the 8, 22, 40, and 60 hpi, were identified during the infection. Among the key genes, the most significant enrichment was in the gene encoding the trihydroxynaphthalene reductase (THR1) in the melanin biosynthesis pathway. Both Δ and Δ strains showed varying degrees of reduction of melanin in appressoria and colonies. The pathogenicity of the Δ strain was lost. In addition, six DEGs from and six DEGs from were selected for real-time quantitative PCR (RT-qPCR) to confirm the RNA-seq results. The information gathered from this study enriches the resources available for research into the role of the gene during the infection of by , such as potential links between melanin biosynthesis and autophagy, and the response of to different fungal strains, thereby providing a theoretical basis for the breeding of cruciferous green leaf vegetable cultivars with resistance to anthracnose disease.
十字花科植物炭疽病由 引起,是一种严重的真菌病害,影响白菜、花椰菜、西兰花、芥菜、拟南芥等十字花科作物。双转录组分析常用于鉴定宿主与病原体相互作用的潜在机制。为了鉴定病原体和宿主中的差异表达基因(DEGs),将野生型(ChWT)和 突变体(Δ)菌株的分生孢子接种到 叶片上,在接种后 8、22、40 和 60 小时(hpi)时对感染的 叶片进行双 RNA-seq 分析。结果表明,在“ChWT”和“Δ”样品之间的基因表达比较中,在 8 hpi 时检测到 900 个 DEGs(306 个上调和 594 个下调),在 22 hpi 时检测到 692 个 DEGs(283 个上调和 409 个下调),在 40 hpi 时检测到 496 个 DEGs(220 个上调和 276 个下调),在 60 hpi 时检测到 3159 个 DEGs(1544 个上调和 1615 个下调)。GO 和 KEGG 分析发现,DEGs 主要参与真菌发育、次生代谢物合成、植物-真菌相互作用和植物激素信号转导。在感染过程中,鉴定了注释在病原体-宿主相互作用数据库(PHI-base)和植物抗性基因数据库(PRGdb)中的关键基因的调控网络,以及与 8、22、40 和 60 hpi 高度相关的一些关键基因。在这些关键基因中,三羟基萘还原酶(THR1)基因在黑色素生物合成途径中的丰度最高。Δ 和 Δ 突变体在附着胞和菌落中的黑色素含量均有不同程度的减少。Δ 菌株的致病性丧失。此外,从 中选择了 6 个 DEGs,从 中选择了 6 个 DEGs,用于实时定量 PCR(RT-qPCR)以验证 RNA-seq 结果。本研究收集的信息丰富了在 侵染过程中基因 作用的研究资源,例如黑色素生物合成与自噬之间的潜在联系,以及 对不同真菌菌株的反应,从而为培育具有抗炭疽病的十字花科绿叶蔬菜品种提供了理论依据。