Xing Baoguang, Li Pengtao, Li Yanfang, Cui Bingkai, Sun Zhihao, Chen Yu, Zhang Shaoliang, Liu Qiankun, Zhang Aiming, Hao Liuan, Du Xue, Liu Xiaoyan, Wu Bei, Peng Renhai, Hu Shoulin
College of Agricultural, Tarim University, Alar 843300, China.
School of Biotechnology and Food Engineering, Anyang Institute of Technology, Anyang 455000, China.
Int J Mol Sci. 2024 Dec 24;26(1):28. doi: 10.3390/ijms26010028.
wilt (VW) caused by (Vd) is a devastating fungal cotton disease characterized by high pathogenicity, widespread distribution, and frequent variation. It leads to significant losses in both the yield and quality of cotton. Identifying key non-synonymous single nucleotide polymorphism (SNP) markers and crucial genes associated with VW resistance in and , and subsequently breeding new disease-resistant varieties, are essential for VW management. Here, we sequenced the transcriptome and metabolome of roots of TM-1 () and Hai7124 () after 0, 1, and 2 days of V991 inoculation. Transcriptome analysis identified a total of 72,752 genes, with 5814 differentially expressed genes (DEGs) determined through multiple group comparisons. KEGG enrichment analysis revealed that the key pathways enriched by DEGs obtained from both longitudinal and transverse comparisons contained the glutathione metabolism pathway. Metabolome analysis identified 995 metabolites, and 22 differentially accumulated metabolites (DAMs), which were correlated to pathways including glutathione metabolism, degradation of valine, leucine, and isoleucine, and biosynthesis of terpenoids, alkaloids, pyridine, and piperidine. The conjoint analysis of transcriptomic and metabolomic sequencing revealed DAMs and DEGs associated with the glutathione metabolism pathway, and the key candidate gene (glutathione S-transferase, ) potentially associated with cotton response to VW infection was selected. These findings establish a basis for investigating the mechanisms underlying the cotton plant's resistance to VW.
由大丽轮枝菌(Vd)引起的棉花枯萎病(VW)是一种毁灭性的真菌病害,具有高致病性、分布广泛和变异频繁的特点。它会导致棉花产量和品质大幅下降。鉴定与棉花抗枯萎病相关的关键非同义单核苷酸多态性(SNP)标记和关键基因,并随后培育新的抗病品种,对于枯萎病的防治至关重要。在此,我们对接种V991后0、1和2天的TM-1(陆地棉)和海7124(海岛棉)根系进行了转录组和代谢组测序。转录组分析共鉴定出72752个基因,通过多组比较确定了5814个差异表达基因(DEG)。KEGG富集分析表明,纵向和横向比较获得的DEG富集的关键途径都包含谷胱甘肽代谢途径。代谢组分析鉴定出995种代谢物和22种差异积累代谢物(DAM),它们与谷胱甘肽代谢、缬氨酸、亮氨酸和异亮氨酸降解以及萜类、生物碱、吡啶和哌啶生物合成等途径相关。转录组和代谢组测序的联合分析揭示了与谷胱甘肽代谢途径相关的DAM和DEG,并筛选出了可能与棉花对枯萎病感染反应相关的关键候选基因GhGSTU24(谷胱甘肽S-转移酶)。这些发现为研究棉花植株抗枯萎病的机制奠定了基础。