铜诱导的应激机制:对铜敏感和耐铜菌株的比较表型和转录组学研究。

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Ricardo Delgado Santander, Srđan G Aćimović
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引用次数: 0

摘要

引起苹果和梨的火枯病。在管理策略中,铜基治疗被广泛用于控制疾病。然而,铜对病原菌的影响并不均匀,不同菌株对重金属的耐受程度不同。在鉴定出具有异常高(EaR2和Ea17)和中等(Ea19)铜敏感性的amylovora菌株后,我们进行了表型和转录组学分析,以了解这些差异的基础。对铜高度敏感的菌株EaR2和Ea17生长速度较慢,对百草枯和镉的敏感性增加,并产生了典型的铜依赖性淀粉样肽和利凡的过量生产,这在菌株Ea273中没有观察到,具有常规的铜耐受性。铜敏感性也与生长期间铜预暴露后较高的铜休克死亡率有关。通过RNA-Seq转录组学分析显示,EaR2和Ea273对铜休克的反应相似,但在铜适应(长时间的铜生长)过程中的转录组学反应截然不同。EaR2通过早期激活应激反应、胞外多糖生物合成途径和蛋白质质量控制系统来响应铜的适应,同时降低与铁摄取相关的基因的表达。Ea273主要表现为铜稳态相关基因的激活,具有组氨酸分解代谢的下调特征。重要意义本研究首次鉴定并鉴定了铜敏感的E. amylovora菌株,为研究火疫病毒体内铜稳态和解毒机制提供了重要的见解。我们的研究有助于更广泛地了解细菌对铜的适应性,以及表型性状和对铜的转录组反应之间的联系。此外,我们的发现为未来优化铜基治疗和未来开发更有效的疾病控制方法奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Copper-induced stress mechanisms in Erwinia amylovora: a comparative phenotypic and transcriptomic study using copper-sensitive and -tolerant strains.

Erwinia amylovora causes fire blight of apple and pear. Among the management strategies, copper-based treatments are widely used to control the disease. However, the impact of copper on the pathogen is not uniform, and different strains show different tolerance levels to the heavy metal. Upon identifying E. amylovora strains with unusually high (EaR2 and Ea17) and intermediate (Ea19) copper sensitivity, we conducted phenotypic and transcriptomic analyses to understand the basis of these differences. The highly copper-sensitive strains EaR2 and Ea17 grew slower, showed increased sensitivity to paraquat and cadmium, and developed a characteristic copper-dependent overproduction of amylovoran and levan, with patterns not observed in strain Ea273, with regular copper tolerance. Copper sensitivity was also associated with higher copper-shock death rates after copper pre-exposure during growth. Transcriptomic analysis via RNA-Seq revealed similar responses to copper shock in EaR2 and Ea273 but very different transcriptomic responses during copper adaptation (prolonged growth with copper). EaR2 responded to copper adaptation with earlier activation of stress responses, exopolysaccharide biosynthesis pathways, and protein quality control systems, while reducing the expression of genes linked to iron uptake. Ea273 mostly displayed an activation of copper homeostasis-related genes, with a characteristic downregulation of histidine catabolism.IMPORTANCEThis study identified and characterized, for the first time, copper hypersensitive E. amylovora strains, providing critical insights into the mechanisms of copper homeostasis and detoxification in the fire blight pathogen. Our study contributes to a broader understanding of bacterial adaptation to copper as well as the connection between phenotypic traits and transcriptomic responses to copper. Furthermore, our findings set the basis for future optimization of copper-based treatments and future development of more effective disease control methods.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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