Abstract

Stilbenes are central phytoalexins in Vitis, and induction of the key enzyme stilbene synthase (STS) is pivotal for disease resistance. Here, we address the potential for breeding resistance using an STS allele isolated from Chinese wild grapevine Vitis pseudoreticulata (VpSTS) by comparison with its homologue from Vitis vinifera cv. 'Carigane' (VvSTS). Although the coding regions of both alleles are very similar (>99% identity on the amino acid level), the promoter regions are significantly different. By expression in Arabidopsis as a heterologous system, we show that the allele from the wild Chinese grapevine can confer accumulation of stilbenes and resistance against the powdery mildew Golovinomyces cichoracearum, whereas the allele from the vinifera cultivar cannot. To dissect the upstream signalling driving the activation of this promoter, we used a dual-luciferase reporter system in a grapevine cell culture. We show elevated responsiveness of the promoter from the wild grape to salicylic acid (SA) and to the pathogen-associated molecular pattern (PAMP) flg22, equal induction of both alleles by jasmonic acid (JA), and a lack of response to the cell death-inducing elicitor Harpin. This elevated SA response of the VpSTS promoter depends on calcium influx, oxidative burst by RboH, mitogen-activated protein kinase (MAPK) signalling, and JA synthesis. We integrate the data in the context of a model where the resistance of V. pseudoreticulata is linked to a more efficient recruitment of SA signalling for phytoalexin synthesis.

Highlights

  • As one of the most ancient crops, grapevine (Vitis vinifera L.) is of economic and cultural significance

  • The PCRamplified fragment of V. pseudoreticulata (VpSTS) was 3802 bp in length, of which the promoter accounted for 2264 bp, while the fragment amplified from V. vinifera cv

  • Comparison of the two promoters with respect to predicted cis-regulatory elements revealed that both promoter alleles shared somef putative stress-responsive elements: WBOXATNPR1 was reported to confer a response to salicylic acid (SA) (Yu et al, 2001); WBOXNTERF3 has been shown to drive response to wounding (Nishiuchi et al, 2004); CCAATBOX1 is linked to responsiveness to heat (Rieping et al, 1992); CBFHV has been shown to be the binding site for CBF1 during the response to dehydration (Xue et al, 2002); MYBCORE was found to be involved in the regulation of flavonoid biosynthesis (Solano et al, 1995); and GT1GMSCAM4 has been linked to the response to salt and biotic stress (Park et al, 2004)

Read more

Summary

Introduction

As one of the most ancient crops, grapevine (Vitis vinifera L.) is of economic and cultural significance. This crop is challenged by several diseases such as downy and powdery mildew, leading to a requirement for intensive plant protection. ~70% of European fungicide production is used for viticulture (Eurostat, 2007). This expensive application produces a negative ecological footprint, and is far from sustainable due to the rapid spread of fungicide resistance through the pathogen population. Resistance breeding has been the most successful strategy for sustainable. The success of these resistant varieties is progressively challenged by the occurrence of new pathogen strains that have already acquired strategies to circumvent the resistance mediated by these resistance loci (Peressotti et al, 2010; Gómez-Zeledón et al, 2013), stimulating the search for alternative mechanisms of resistance

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.