Brustolini Otávio J B, Machado Joao Paulo B, Condori-Apfata Jorge A, Coco Daniela, Deguchi Michihito, Loriato Virgílio A P, Pereira Welison A, Alfenas-Zerbini Poliane, Zerbini Francisco M, Inoue-Nagata Alice K, Santos Anesia A, Chory Joanne, Silva Fabyano F, Fontes Elizabeth P B
Departamento de Bioquímica e Biologia Molecular, Bioagro, Viçosa, MG, Brazil.
National Institute of Science and Technology in Plant-Pest Interactions, Bioagro, Viçosa, MG, Brazil.
Plant Biotechnol J. 2015 Dec;13(9):1300-1311. doi: 10.1111/pbi.12349. Epub 2015 Feb 16.
Begomovirus-associated epidemics currently threaten tomato production worldwide due to the emergence of highly pathogenic virus species and the proliferation of a whitefly B biotype vector that is adapted to tomato. To generate an efficient defence against begomovirus, we modulated the activity of the immune defence receptor nuclear shuttle protein (NSP)-interacting kinase (NIK) in tomato plants; NIK is a virulence target of the begomovirus NSP during infection. Mutation of T474 within the kinase activation loop promoted the constitutive activation of NIK-mediated defences, resulting in the down-regulation of translation-related genes and the suppression of global translation. Consistent with these findings, transgenic lines harbouring an activating mutation (T474D) were tolerant to the tomato-infecting begomoviruses ToYSV and ToSRV. This phenotype was associated with reduced loading of coat protein viral mRNA in actively translating polysomes, lower infection efficiency and reduced accumulation of viral DNA in systemic leaves. Our results also add some relevant insights into the mechanism underlying the NIK-mediated defence. We observed that the mock-inoculated T474D-overexpressing lines showed a constitutively infected wild-type transcriptome, indicating that the activation of the NIK-mediated signalling pathway triggers a typical response to begomovirus infection. In addition, the gain-of-function mutant T474D could sustain an activated NIK-mediated antiviral response in the absence of the virus, further confirming that phosphorylation of Thr-474 is the crucial event that leads to the activation of the kinase.
由于高致病性病毒种类的出现以及适应番茄的烟粉虱B生物型载体的扩散,与双生病毒相关的流行病目前正威胁着全球番茄生产。为了产生对双生病毒的有效防御,我们调节了番茄植株中免疫防御受体核穿梭蛋白(NSP)相互作用激酶(NIK)的活性;NIK是双生病毒感染期间NSP的毒力靶点。激酶激活环内T474的突变促进了NIK介导防御的组成型激活,导致翻译相关基因的下调和整体翻译的抑制。与这些发现一致,携带激活突变(T474D)的转基因株系对感染番茄的双生病毒ToYSV和ToSRV具有耐受性。这种表型与主动翻译多聚体中衣壳蛋白病毒mRNA的负载减少、感染效率降低以及系统叶中病毒DNA的积累减少有关。我们的结果还为NIK介导防御的潜在机制提供了一些相关见解。我们观察到,模拟接种的过表达T474D的株系表现出组成型感染的野生型转录组,表明NIK介导的信号通路的激活触发了对双生病毒感染的典型反应。此外,功能获得性突变体T474D在没有病毒的情况下可以维持激活的NIK介导的抗病毒反应,进一步证实Thr-474的磷酸化是导致激酶激活的关键事件。