Department of Plant Sciences, University of California, Davis, CA 95616, USA.
Departamento de Ciências Biológicas, Instituto de Ciências Exatas e Biológicas, Núcleo de Pesquisas em Ciências Biológicas, Universidade Federal de Ouro Preto, Ouro Preto 35400-000, Brazil.
Int J Mol Sci. 2020 Oct 9;21(20):7453. doi: 10.3390/ijms21207453.
The interaction between the plant host, walnut (; Jr), and a deadly pathogen ( pv. 417; Xaj) can lead to walnut bacterial blight (WB), which depletes walnut productivity by degrading the nut quality. Here, we dissect this pathosystem using tandem mass tag quantitative proteomics. Walnut hull tissues inoculated with Xaj were compared to mock-inoculated tissues, and 3972 proteins were identified, of which 3296 are from Jr and 676 from Xaj. Proteins with differential abundance include oxidoreductases, proteases, and enzymes involved in energy metabolism and amino acid interconversion pathways. Defense responses and plant hormone biosynthesis were also increased. Xaj proteins detected in infected tissues demonstrate its ability to adapt to the host microenvironment, limiting iron availability, coping with copper toxicity, and maintaining energy and intermediary metabolism. Secreted proteases and extracellular secretion apparatus such as type IV pilus for twitching motility and type III secretion effectors indicate putative factors recognized by the host. Taken together, these results suggest intense degradation processes, oxidative stress, and general arrest of the biosynthetic metabolism in infected nuts. Our results provide insights into molecular mechanisms and highlight potential molecular tools for early detection and disease control strategies.
植物宿主胡桃(Jr)与致命病原体(pv. 417; Xaj)之间的相互作用可导致胡桃细菌性枯萎病(WB),从而降低坚果质量,降低胡桃生产力。在这里,我们使用串联质量标签定量蛋白质组学来剖析这个病理系统。用 Xaj 接种胡桃壳组织与模拟接种组织进行比较,鉴定出 3972 种蛋白质,其中 3296 种来自 Jr,676 种来自 Xaj。丰度差异的蛋白质包括氧化还原酶、蛋白酶和参与能量代谢及氨基酸转化途径的酶。防御反应和植物激素生物合成也增加了。在感染组织中检测到的 Xaj 蛋白表明其能够适应宿主微环境,限制铁的可用性,应对铜毒性,并维持能量和中间代谢。分泌的蛋白酶和细胞外分泌装置,如用于蠕动运动的 IV 型菌毛和 III 型分泌效应器,表明宿主识别的潜在因素。总之,这些结果表明感染坚果中存在强烈的降解过程、氧化应激和生物合成代谢的普遍停滞。我们的研究结果为分子机制提供了深入了解,并突出了早期检测和疾病控制策略的潜在分子工具。