Babińska-Wensierska Weronika, Motyka-Pomagruk Agata, Mengoni Alessio, diCenzo George C, Lojkowska Ewa
Laboratory of Plant Protection and Biotechnology, Intercollegiate Faculty of Biotechnology, University of Gdansk and Medical University of Gdansk, 58 Abrahama, Gdansk, 80-307, Poland.
Laboratory of Physical Biochemistry, Intercollegiate Faculty of Biotechnology University of Gdansk and Medical University of Gdansk, University of Gdansk, 58 Abrahama, Gdansk, 80-307, Poland.
Sci Rep. 2025 Apr 25;15(1):14531. doi: 10.1038/s41598-025-98321-4.
Dickeya solani causes soft rot and blackleg mainly on potato crops. High pathogenicity of this species results from efficient production of plant cell wall-degrading enzymes, especially pectate lyases, potent root colonization, and fast vascular movement. Despite genomic homogeneity, variations in virulence-related phenotypes suggest differences in the gene expression patterns between diverse strains. Therefore, the methylomes and transcriptomes of two strains (virulent IFB0099 and low virulent IFB0223), differing in tissue maceration capacity and virulence factors production, have been studied. Methylation analysis revealed no significant differences. However, the analysis of transcriptomes, studied under both non-induced and induced by polygalacturonic acid conditions (in order to mimic diverse stages of plant infection process), unveiled higher expression of pectate lyases (pelD, pelE, pelL), pectin esterase (pemA), proteases (prtE, prtD) and Vfm-associated quorum-sensing genes (vfmC, vfmD, vfmE) in IFB0099 strain compared to IFB0223. Additionally, the genes related to the secretion system II (T2SS) (gspJ, nipE) displayed higher induction of expression in IFB0099. Furthermore, IFB0099 showed more elevated expression of genes involved in flagella formation, which coincides with enhanced motility and pathogenicity of this strain compared to IFB0223. To sum up, differential expression analysis of genes important for the virulence of D. solani indicated candidate genes, which might be crucial for the pathogenicity of this species.
索拉尼果胶杆菌主要引起马铃薯作物的软腐病和黑胫病。该菌种的高致病性源于其高效产生植物细胞壁降解酶,尤其是果胶酸裂解酶、强大的根部定殖能力以及快速的维管束移动能力。尽管基因组具有同质性,但与毒力相关的表型差异表明不同菌株之间基因表达模式存在差异。因此,对两株在组织浸解能力和毒力因子产生方面存在差异的菌株(强毒株IFB0099和弱毒株IFB0223)的甲基化组和转录组进行了研究。甲基化分析未发现显著差异。然而,在未诱导和经聚半乳糖醛酸诱导的条件下(为模拟植物感染过程的不同阶段)对转录组进行分析发现,与IFB0223相比,IFB0099菌株中果胶酸裂解酶(pelD、pelE、pelL)、果胶酯酶(pemA)、蛋白酶(prtE、prtD)以及与Vfm相关的群体感应基因(vfmC、vfmD、vfmE)的表达更高。此外,与Ⅱ型分泌系统(T2SS)相关的基因(gspJ、nipE)在IFB0099中表现出更高的表达诱导。此外,IFB0099中参与鞭毛形成的基因表达水平更高,这与该菌株相比IFB0223增强的运动性和致病性相一致。总之,对索拉尼果胶杆菌毒力重要基因的差异表达分析表明了一些候选基因,这些基因可能对该菌种的致病性至关重要。