Spray-induced gene silencing (SIGS) as a tool for the management of Pine Pitch Canker forest disease

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Abstract

Global change is exacerbating the prevalence of plant diseases caused by pathogenic fungi in forests worldwide. The conventional use of chemical fungicides, which is commonplace in agricultural settings, is not sanctioned for application in forest ecosystems, so novel control strategies are imperative. The promising approach SIGS (Spray-Induced Gene Silencing) involves the external application of specific double-stranded RNA (dsRNA), which can modulate the expression of target genes through environmental RNA interference in eukaryotes. SIGS exhibited notable success in reducing virulence when deployed against some crop fungal pathogens, such as Fusarium graminearum , Botrytis cinerea and Sclerotinia sclerotiorum , among others. However, there is a conspicuous dearth of studies evaluating the applicability of SIGS for managing forest pathogens. This research aimed to determine whether SIGS could be used to control Fusarium circinatum , a widely impactful forest pathogen that causes Pine Pitch Canker disease. To achieve this, we designed and produced though a bacterial synthesis, dsRNA molecules to target fungal essential genes involved to vesicle trafficking ( Vps51 , DCTN1 , and SAC1 ), signal transduction ( Pp2a , Sit4 , Ppg1 , and Tap42 ), and cell wall biogenesis ( Chs1 , Chs2 , Chs3b , Gls1 ) metabolic pathways. We confirmed that F. circinatum is able to uptake externally applied dsRNA, triggering an inhibition of the pathogen’s virulence. Furthermore, this study pioneers the demonstration that recurrent applications of dsRNAs in SIGS are more effective in protecting plants than single applications. Therefore, SIGS emerges as an effective and sustainable approach for managing plant pathogens, showcasing its efficacy in controlling a globally significant forest pathogen subject to quarantine measures.

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