Chemical Biology Laboratory, Max Planck Institute of Plant Breeding Research, Carl-von-Linnè-Weg 10, 50829, Köln, Germany.
Chemical Biology, Centre of Medical Biotechnology, Faculty of Biology, University of Duisburg-Essen, Universitätsstr. 2, 45141, Essen, Germany.
Sci Rep. 2019 Aug 1;9(1):11196. doi: 10.1038/s41598-019-47526-5.
In plants, low-dose of exogenous bacterial cyclic lipopeptides (CLPs) trigger transient membrane changes leading to activation of early and late defence responses. Here, a forward chemical genetics approach identifies colistin sulphate (CS) CLP as a novel plant defence inducer. CS uniquely triggers activation of the PATHOGENESIS-RELATED 1 (PR1) gene and resistance against Pseudomonas syringae pv. tomato DC3000 (Pst DC3000) in Arabidopsis thaliana (Arabidopsis) independently of the PR1 classical inducer, salicylic acid (SA) and the key SA-signalling protein, NON-EXPRESSOR OF PR1 (NPR1). Low bioactive concentration of CS does not trigger activation of early defence markers such as reactive oxygen species (ROS) and mitogen activated protein kinase (MAPK). However, it strongly suppresses primary root length elongation. Structure activity relationship (SAR) assays and mode-of-action (MoA) studies show the acyl chain and activation of a ∼46 kDa p38-like kinase pathway to be crucial for CS' bioactivity. Selective pharmacological inhibition of the active p38-like kinase pathway by SB203580 reverses CS' effects on PR1 activation and root length suppression. Our results with CS as a chemical probe highlight the existence of a novel SA- and NPR1-independent branch of PR1 activation functioning via a membrane-sensitive p38-like kinase pathway.
在植物中,低剂量的外源细菌环状脂肽(CLPs)会引发短暂的膜变化,从而激活早期和晚期防御反应。在这里,一种正向化学遗传学方法确定硫酸粘菌素(CS)CLP 是一种新型的植物防御诱导剂。CS 独特地触发拟南芥(Arabidopsis)中与 PR1 经典诱导剂水杨酸(SA)和关键的 SA 信号蛋白 NON-EXPRESSOR OF PR1(NPR1)无关的 PATHOGENESIS-RELATED 1(PR1)基因的激活和对丁香假单胞菌 pv.番茄 DC3000(Pst DC3000)的抗性。CS 的低生物活性浓度不会引发活性氧(ROS)和丝裂原激活蛋白激酶(MAPK)等早期防御标记物的激活。然而,它强烈抑制主根伸长。结构活性关系(SAR)测定和作用方式(MoA)研究表明,酰基链和激活约 46 kDa 的 p38 样激酶途径对 CS 的生物活性至关重要。通过 SB203580 选择性地抑制活性 p38 样激酶途径可逆转 CS 对 PR1 激活和根长抑制的作用。我们使用 CS 作为化学探针的结果突出了存在一条新的、不依赖于 SA 和 NPR1 的 PR1 激活分支,该分支通过膜敏感的 p38 样激酶途径发挥作用。