Sustained NIK-mediated antiviral signalling confers broad-spectrum tolerance to begomoviruses in cultivated plants

• Autor(a) principal: Brustolini, Otávio J.B.
• Data de Publicação: 2015
• Outros Autores: 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.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: LOCUS Repositório Institucional da UFV
• Texto Completo: http://dx.doi.org/10.1111/pbi.12349; http://www.locus.ufv.br/handle/123456789/14850
• topic: NIK; NSP-interacting kinase; Nuclear shuttle protein; Tomato-infecting begomoviruses; Begomovirus; Leucine-rich repeats receptor-like kinase

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.