Alvarez-Diaz Juan C, Laugé Richard, Delannoy Etienne, Huguet Stéphanie, Paysant-Le Roux Christine, Gratias Ariane, Geffroy Valérie
Université Paris-Saclay, CNRS, INRAE, Université Evry, Institute of Plant Sciences Paris-Saclay (IPS2), 91190 Gif sur Yvette, France.
Université Paris-Cité, CNRS, INRAE, Institute of Plant Sciences Paris-Saclay (IPS2), 91190 Gif sur Yvette, France.
Plants (Basel). 2022 Jul 31;11(15):1995. doi: 10.3390/plants11151995.
Bean anthracnose caused by the hemibiotrophic fungus is one of the most important diseases of common bean () in the world. In the present study, the whole transcriptome of common bean infected with during compatible and incompatible interactions was characterized at 48 and 72 hpi, corresponding to the biotrophy phase of the infection cycle. Our results highlight the prominent role of pathogenesis-related (PR) genes from the PR10/Bet vI family as well as a complex interplay of different plant hormone pathways including Ethylene, Salicylic acid (SA) and Jasmonic acid pathways. Gene Ontology enrichment analysis reveals that infected common bean seedlings responded by down-regulation of photosynthesis, ubiquitination-mediated proteolysis and cell wall modifications. In infected common bean, SA biosynthesis seems to be based on the PAL pathway instead of the ICS pathway, contrarily to what is described in . Interestingly, ~30 NLR were up-regulated in both contexts. Overall, our results suggest that the difference between the compatible and incompatible reaction is more a question of timing and strength, than a massive difference in differentially expressed genes between these two contexts. Finally, we used RT-qPCR to validate the expression patterns of several genes, and the results showed an excellent agreement with deep sequencing.
由半活体营养型真菌引起的菜豆炭疽病是世界上普通菜豆()最重要的病害之一。在本研究中,对普通菜豆在亲和与非亲和互作过程中,于接种后48小时和72小时(对应感染周期的活体营养阶段)被感染时的全转录组进行了表征。我们的结果突出了PR10/Bet vI家族中病程相关(PR)基因的显著作用,以及包括乙烯、水杨酸(SA)和茉莉酸途径在内的不同植物激素途径的复杂相互作用。基因本体富集分析表明,受感染的普通菜豆幼苗通过下调光合作用、泛素化介导的蛋白水解和细胞壁修饰做出反应。在受感染的普通菜豆中,SA生物合成似乎基于苯丙氨酸解氨酶(PAL)途径而非异分支酸合成酶(ICS)途径,这与文献中描述的情况相反。有趣的是,在两种情况下约30个核苷酸结合富含亮氨酸重复序列(NLR)基因均上调。总体而言,我们的结果表明,亲和与非亲和反应之间的差异更多是时间和强度的问题,而非这两种情况下差异表达基因的巨大差异。最后,我们使用逆转录定量聚合酶链反应(RT-qPCR)验证了几个基因的表达模式,结果与深度测序显示出极好的一致性。