Shabab Mohammed, Shindo Takayuki, Gu Christian, Kaschani Farnusch, Pansuriya Twinkal, Chintha Raju, Harzen Anne, Colby Tom, Kamoun Sophien, van der Hoorn Renier A L
Plant Chemetics Lab, Max Planck Institute for Plant Breeding Research, 50829 Cologne, Germany.
Plant Cell. 2008 Apr;20(4):1169-83. doi: 10.1105/tpc.107.056325. Epub 2008 Apr 30.
The interaction between the fungal pathogen Cladosporium fulvum and its host tomato (Solanum lycopersicum) is an ideal model to study suppression of extracellular host defenses by pathogens. Secretion of protease inhibitor AVR2 by C. fulvum during infection suggests that tomato papain-like cysteine proteases (PLCPs) are part of the tomato defense response. We show that the tomato apoplast contains a remarkable diversity of PLCP activities with seven PLCPs that fall into four different subfamilies. Of these PLCPs, transcription of only PIP1 and RCR3 is induced by treatment with benzothiadiazole, which triggers the salicylic acid-regulated defense pathway. Sequencing of PLCP alleles of tomato relatives revealed that only PIP1 and RCR3 are under strong diversifying selection, resulting in variant residues around the substrate binding groove. The doubled number of variant residues in RCR3 suggests that RCR3 is under additional adaptive selection, probably to prevent autoimmune responses. AVR2 selectively inhibits only PIP1 and RCR3, and one of the naturally occurring variant residues in RCR3 affects AVR2 inhibition. The higher accumulation of PIP1 protein levels compared with RCR3 indicates that PIP1 might be the real virulence target of AVR2 and that RCR3 acts as a decoy for AVR2 perception in plants carrying the Cf-2 resistance gene.
真菌病原体番茄叶霉(Cladosporium fulvum)与其宿主番茄(Solanum lycopersicum)之间的相互作用是研究病原体对宿主细胞外防御抑制作用的理想模型。番茄叶霉在感染期间分泌蛋白酶抑制剂AVR2,这表明番茄木瓜蛋白酶样半胱氨酸蛋白酶(PLCPs)是番茄防御反应的一部分。我们发现番茄质外体中存在多种PLCP活性,其中七种PLCP可分为四个不同的亚家族。在这些PLCP中,只有PIP1和RCR3的转录受到苯并噻二唑处理的诱导,苯并噻二唑可触发水杨酸调节的防御途径。番茄近缘种PLCP等位基因的测序表明,只有PIP1和RCR3受到强烈的多样化选择,导致底物结合槽周围出现变异残基。RCR3中变异残基数量的增加表明RCR3受到额外的适应性选择,可能是为了防止自身免疫反应。AVR2仅选择性抑制PIP1和RCR3,RCR3中一个天然存在的变异残基影响AVR2的抑制作用。与RCR3相比,PIP1蛋白水平的积累更高,这表明PIP1可能是AVR2的真正毒力靶标,而RCR3在携带Cf-2抗性基因的植物中作为AVR2识别的诱饵。