Song Jing, Win Joe, Tian Miaoying, Schornack Sebastian, Kaschani Farnusch, Ilyas Muhammad, van der Hoorn Renier A L, Kamoun Sophien
Department of Plant Pathology, The Ohio State University, Ohio Agricultural Research and Development Center, Wooster, OH 44691, USA.
Proc Natl Acad Sci U S A. 2009 Feb 3;106(5):1654-9. doi: 10.1073/pnas.0809201106. Epub 2009 Jan 26.
Current models of plant-pathogen interactions stipulate that pathogens secrete effector proteins that disable plant defense components known as virulence targets. Occasionally, the perturbations caused by these effectors trigger innate immunity via plant disease resistance proteins as described by the "guard hypothesis." This model is nicely illustrated by the interaction between the fungal plant pathogen Cladosporium fulvum and tomato. C. fulvum secretes a protease inhibitor Avr2 that targets the tomato cysteine protease Rcr3(pim). In plants that carry the resistance protein Cf2, Rcr3(pim) is required for resistance to C. fulvum strains expressing Avr2, thus fulfilling one of the predictions of the guard hypothesis. Another prediction of the guard hypothesis has not yet been tested. Considering that virulence targets are important components of defense, different effectors from unrelated pathogens are expected to evolve to disable the same host target. In this study we confirm this prediction using a different pathogen of tomato, the oomycete Phytophthora infestans that is distantly related to fungi such as C. fulvum. This pathogen secretes an array of protease inhibitors including EPIC1 and EPIC2B that inhibit tomato cysteine proteases. Here we show that, similar to Avr2, EPIC1 and EPIC2B bind and inhibit Rcr3(pim). However, unlike Avr2, EPIC1 and EPIC2B do not trigger hypersensitive cell death or defenses on Cf-2/Rcr3(pim) tomato. We also found that the rcr3-3 mutant of tomato that carries a premature stop codon in the Rcr3 gene exhibits enhanced susceptibility to P. infestans, suggesting a role for Rcr3(pim) in defense. In conclusion, our findings fulfill a key prediction of the guard hypothesis and suggest that the effectors Avr2, EPIC1, and EPIC2B secreted by two unrelated pathogens of tomato target the same defense protease Rcr3(pim). In contrast to C. fulvum, P. infestans appears to have evolved stealthy effectors that carry inhibitory activity without triggering plant innate immunity.
当前植物与病原体相互作用的模型表明,病原体分泌效应蛋白,这些蛋白会使被称为毒力靶标的植物防御成分失效。偶尔,这些效应蛋白引起的干扰会通过植物抗病蛋白触发先天免疫,这就是“守卫假说”所描述的情况。真菌植物病原体番茄叶霉与番茄之间的相互作用很好地说明了这一模型。番茄叶霉分泌一种蛋白酶抑制剂Avr2,其作用靶点是番茄半胱氨酸蛋白酶Rcr3(pim)。在携带抗病蛋白Cf2的植物中,Rcr3(pim)是抵抗表达Avr2的番茄叶霉菌株所必需的,从而证实了守卫假说的一个预测。守卫假说的另一个预测尚未得到验证。鉴于毒力靶标是防御的重要组成部分,预计来自不相关病原体的不同效应蛋白会进化以作用于同一宿主靶标。在本研究中,我们使用番茄的另一种病原体——与番茄叶霉等真菌亲缘关系较远的卵菌致病疫霉,证实了这一预测。这种病原体分泌一系列蛋白酶抑制剂,包括抑制番茄半胱氨酸蛋白酶的EPIC1和EPIC2B。我们在此表明,与Avr2类似,EPIC1和EPIC2B结合并抑制Rcr3(pim)。然而,与Avr2不同的是,EPIC1和EPIC2B不会在Cf - 2/Rcr3(pim)番茄上引发超敏细胞死亡或防御反应。我们还发现,在Rcr3基因中携带提前终止密码子的番茄rcr3 - 3突变体对致病疫霉的易感性增强,这表明Rcr3(pim)在防御中发挥作用。总之,我们的研究结果证实了守卫假说的一个关键预测,并表明番茄的两种不相关病原体分泌的效应蛋白Avr2、EPIC1和EPIC2B作用于同一防御蛋白酶Rcr3(pim)。与番茄叶霉不同,致病疫霉似乎进化出了隐秘的效应蛋白,这些蛋白具有抑制活性但不会触发植物先天免疫。