Overexpression of VqWRKY31 enhances powdery mildew resistance in grapevine by promoting salicylic acid signaling and specific metabolite synthesis

Wuchen Yin , Xianhang Wang , Hui Liu , Ya Wang , Steve van Nocker , Mingxing Tu , Jinghao Fang , Junqiang Guo , Zhi Li , Xiping Wang

Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) : uhab064

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Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) :uhab064 DOI: 10.1093/hr/uhab064
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Overexpression of VqWRKY31 enhances powdery mildew resistance in grapevine by promoting salicylic acid signaling and specific metabolite synthesis
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Abstract

Powdery mildew (PM), caused by the fungal pathogen Erysiphe necator , is one of the most destructive diseases of grapevine (Vitis vinifera and other Vitis spp.). Resistance to PM is an important goal for cultivar improvement, and understanding the underlying molecular mechanisms conditioning resistance is critical. Here, we report that transgenic expression of the WRKY transcription factor gene VqWRKY31 from the PM-resistant species Vitis quinquangularis conferred resistance to PM in V. vinifera through promoting salicylic acid signaling and specific metabolite synthesis. VqWRKY31 belongs to the WRKY IIb subfamily, and expression of the VqWRKY31 gene was induced in response to E. necator inoculation. Transgenic V. vinifera plants expressing VqWRKY31 were substantially less susceptible to E. necator infection, and this was associated with increased levels of salicylic acid and reactive oxygen species. Correlation analysis of transcriptomic and metabolomic data revealed that VqWRKY31 promoted expression of genes in metabolic pathways and the accumulation of many disease resistance-related metabolites, including stilbenes, flavonoids, and proanthocyanidins. In addition, results indicated that VqWRKY31 can directly bind to the promoters of two structural genes in stilbene synthesis, STS9 and STS48, and activate their expression. Based on our results, we propose a model where VqWRKY31 enhances grapevine PM resistance through activation of salicylic acid defense signaling and promotion of specific disease resistance- related metabolite synthesis. These findings can be directly exploited for molecular breeding strategies to produce PM-resistant grapevine germplasm.

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Wuchen Yin, Xianhang Wang, Hui Liu, Ya Wang, Steve van Nocker, Mingxing Tu, Jinghao Fang, Junqiang Guo, Zhi Li, Xiping Wang. Overexpression of VqWRKY31 enhances powdery mildew resistance in grapevine by promoting salicylic acid signaling and specific metabolite synthesis. Horticulture Research, 2022, 9 (1) : uhab064 DOI:10.1093/hr/uhab064

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References

[1]

Qiu W, Feechan A, Dry I . Current understanding of grapevine defense mechanisms against the biotrophic fungus (Erysiphe necator), the causal agent of powdery mildew disease . Hortic Res. 2015; 2: 15020.

[2]

Taksonyi P, Kocsis L, Matyas KK et al. The effect of quinone outside inhibitor fungicides on powdery mildew in a grape vineyard in Hungary. Sci Hortic. 2013; 161: 233-8.

[3]

Wan Y, Schwaninger H, He P et al. Comparison of resistance to powdery mildew and downy mildew in Chinese wild grapes. Vitis. 2007; 46: 132-6.

[4]

Cadle-Davidson L, Chicoine DR, Consolie NH . Variation within and among Vitis spp. for foliar resistance to the powdery mildew pathogen Erysiphe necator . Plant Dis. 2011; 95: 202-11.

[5]

Olmo HP . The potential role of (vinifera x rotundifolia) hybrids in grape variety improvement. Experientia. 1986; 42: 921-6.

[6]

Zhu Z, Shi J, Xu W et al. Three ERF transcription factors from Chinese wild grapevine Vitis pseudoreticulata participate in different biotic and abiotic stress-responsive pathways. J Plant Physiol. 2013; 170: 923-33.

[7]

Yu Y, Guo D, Li G et al. The grapevine R2R3-type MYB transcription factor VdMYB1 positively regulates defense responses by activating the stilbene synthase gene 2 (VdSTS2). BMC Plant Biol. 2019; 19: 478.

[8]

Wang D, Jiang C, Liu W et al. The WRKY53 transcription factor enhances stilbene synthesis and disease resistance by interacting with MYB14 and MYB15 in Chinese wild grape. J Exp Bot. 2020; 71: 3211-26.

[9]

Wang X, Guo R, Tu M et al. Ectopic expression of the wild grape WRKY transcription factor VqWRKY52 in Arabidopsis thaliana enhances resistance to the biotrophic pathogen powdery mildew but not to the necrotrophic pathogen Botrytis cinerea . Front Plant Sci. 2017; 8: 97.

[10]

Zhang Y, Li X . Salicylic acid: biosynthesis, perception, and contributions to plant immunity. Curr Opin Plant Biol. 2019; 50: 29-36.

[11]

Coll NS, Epple P, Dangl JL . Programmed cell death in the plant immune system. Cell Death Differ. 2011; 18: 1247-56.

[12]

Muthamilarasan M, Prasad M . Plant innate immunity: an updated insight into defense mechanism. J Biosci. 2013; 38: 433-49.

[13]

Torres MA . ROS in biotic interactions. Physiol Plant. 2010; 138: 414-29.

[14]

Jeandet P, Courot E, Clément C et al. Molecular engineering of phytoalexins in plants: benefits and limitations for food and agriculture. J Agric Food Chem. 2017; 65: 2643-4.

[15]

Leckband G, Lorz H . Transformation and expression of a stilbene synthase gene of Vitis vinifera L. in barley and wheat for increased fungal resistance. Theor Appl Genet. 1998; 96: 1004-12.

[16]

Xu W, Fuli M, Li R et al. VpSTS29/STS2 enhances fungal tolerance in grapevine through a positive feedback loop. Plant Cell Environ. 2019; 42: 2979-98.

[17]

Wang Y, Wang D, Wang F et al. Expression of the grape VaSTS19 gene in Arabidopsis improves resistance to powdery mildew and Botrytis cinerea but increases susceptibility to Pseudomonas syringe pv tomato DC3000 . Int J Mol Sci. 2017; 18: 2000.

[18]

Schnee S, Viret O, Gindro K . Role of stilbenes in the resistance of grapevine to powdery mildew. Physiol Mol Plant Pathol. 2008; 72: 128-33.

[19]

Chang X, Heene E, Qiao F et al. The phytoalexin resveratrol regulates the initiation of hypersensitive cell death in Vitis cell. PLoS One. 2011; 6: e26405.

[20]

Jia Z, Zou B, Wang X et al. Quercetin-induced H2O2 mediates the pathogen resistance against Pseudomonas syringae pv. Tomato DC3000 in Arabidopsis thaliana . Biochem Biophys Res Commun. 2010; 396: 522-7.

[21]

Wang YC, Qian W-J, Li N-N et al. Metabolic changes of caffeine in tea plant (Camellia sinensis (L.) O. Kuntze) as defense response to Colletotrichum fructicola . J Agric Food Chem. 2016; 64: 6685-93.

[22]

Padmavati M, Sakthivel N, Thara KV et al. Differential sensitivity of rice pathogens to growth inhibition by flavonoids. Phytochemistry. 1997; 46: 499-502.

[23]

Feng J, Zhang M, Yang K-N et al. Salicylic acid-primed defence response in octoploid strawberry ‘Benihoppe’ leaves induces resistance against Podosphaera aphanis through enhanced accumulation of proanthocyanidins and upregulation of pathogenesis-related genes. BMC Plant Biol. 2020; 20: 149.

[24]

Dixon RA, Xie DY, Sharma SB . Proanthocyanidins - a final frontier in flavonoid research? New Phytol. 2005; 165: 9-28.

[25]

Azuma A, Yakushiji H, Koshita Y et al. Flavonoid biosynthesis-related genes in grape skin are differentially regulated by temperature and light conditions. Planta. 2012; 236: 1067-80.

[26]

Strissel T, Halbwirth H, Hoyer U et al. Growth-promoting nitrogen nutrition affects flavonoid biosynthesis in young apple (Malus domestica Borkh.) leaves . Plant Biol (Stuttg). 2005; 7: 677-85.

[27]

Hu Y, Dong Q, Yu D . Arabidopsis WRKY46 coordinates with WRKY70 and WRKY53 in basal resistance against pathogen Pseudomonas syringae . Plant Sci. 2012; 185: 288-97.

[28]

Birkenbihl RP, Diezel C, Somssich IE . Arabidopsis WRKY33 is a key transcriptional regulator of hormonal and metabolic responses toward Botrytis cinerea infection . Plant Physiol. 2012; 159: 266-85.

[29]

Bi M, Li X, Yan X et al. Chrysanthemum WRKY15-1 promotes resistance to Puccinia horiana Henn. via the salicylic acid signaling pathway. Hortic Res. 2021; 8: 6.

[30]

Fan S, Dong L, Han D et al. GmWRKY31 and GmHDL56 enhances resistance to Phytophthora sojae by regulating defense-related gene expression in soybean. Front Plant Sci. 2017; 8: 781.

[31]

Wang X, Tu M, Wang Y et al. Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine. Hortic Res. 2021; 8: 114.

[32]

Yu Y, Xu W, Wang J et al. The Chinese wild grapevine (Vitis pseudoreticulata) E3 ubiquitin ligase Erysiphe necator-induced RING finger protein 1 (EIRP1) activates plant defense responses by inducing proteolysis of the VpWRKY11 transcription factor. New Phytol. 2013; 200: 834-46.

[33]

Gao Y-R, Han Y-T, Zhao F-L et al. Identification and utilization of a new Erysiphe necator isolate NAFU1 to quickly evaluate powdery mildew resistance in wild Chinese grapevine species using detached leaves. Plant Physiol Biochem. 2016; 98: 12-24.

[34]

Driever SM, Fryer MJ, Mullineaux PM et al. Imaging of reactive oxygen species in vivo. Methods Mol Biol. 2009; 479: 109-16.

[35]

Hu Y, Gao Y-R, Yang L-S et al. The cytological basis of powdery mildew resistance in wild Chinese Vitis species. Plant Physiol Biochem. 2019; 144: 244-53.

[36]

Wang R, He F, Ning Y et al. Fine-tuning of RBOH-mediated ROS signaling in plant immunity. Trends Plant Sci. 2020; 25: 1060-2.

[37]

Robatzek S, Somssich IE . A new member of the Arabidopsis WRKY transcription factor family, AtWRKY6, is associated with both senescence- and defence-related processes. Plant J. 2001; 28: 123-33.

[38]

Bhattarai KK, Atamian HS, Kaloshian I et al. WRKY72-type transcription factors contribute to basal immunity in tomato and Arabidopsis as well as gene-for-gene resistance mediated by the tomato R gene mi-1 . Plant J. 2010; 63: 229-40.

[39]

Gu KD, Zhang QY, Yu JQ et al. R2R3-MYB transcription factor MdMYB73 confers increased resistance to the fungal pathogen Botryosphaeria dothidea in apples via the salicylic acid pathway. J Agric Food Chem. 2021; 69: 447-58.

[40]

Wang NN, Li Y, Chen Y-H et al. Phosphorylation of WRKY16 by MPK3-1 is essential for its transcriptional activity during fiber initiation and elongation in cotton (Gossypium hirsutum) . Plant Cell. 2021; 33: 2736-52.

[41]

Zhang G, Yan X, Zhang S et al. The jasmonate-ZIM domain gene VqJAZ4 from the Chinese wild grape Vitis quinquangularis improves resistance to powdery mildew in Arabidopsis thaliana . Plant Physiol Biochem. 2019; 143: 329-39.

[42]

Hu Y, Li Y, Hou F et al. Ectopic expression of Arabidopsis broad-spectrum resistance gene RPW8.2 improves the resistance to powdery mildew in grapevine (Vitis vinifera) . Plant Sci. 2018; 267: 20-31.

[43]

Jiao Y, Xu W, Duan D et al. A stilbene synthase allele from a Chinese wild grapevine confers resistance to powdery mildew by recruiting salicylic acid signalling for efficient defence. J Exp Bot. 2016; 67: 5841-56.

[44]

Fung RW, Gonzalo M, Fekete C et al. Powdery mildew induces defense-oriented reprogramming of the transcriptome in a susceptible but not in a resistant grapevine. Plant Physiol. 2008; 146: 236-49.

[45]

Gao F, Dai R, Pike SM et al. Functions of EDS1-like and PAD4 genes in grapevine defenses against powdery mildew. Plant Mol Biol. 2014; 86: 381-93.

[46]

Dai L, Wang D, Xie X et al. The novel gene VpPR4-1 from Vitis pseudoreticulata increases powdery mildew resistance in transgenic Vitis vinifera L. Front Plant Sci. 2016; 7: 695.

[47]

Chong Y, Lee HL, Song J et al. Biosynthesis of resveratrol derivatives and evaluation of their anti-inflammatory activity. Appl Biol Chem. 2021; 64: 33.

[48]

Pezet R, Gindro K, Viret O et al. Effects of resveratrol, viniferins and pterostilbene on Plasmopara viticola zoospore mobility and disease development. Vitis. 2004; 43: 145-8.

[49]

Dercks W, Creasy LL . The significance of stilbene phytoalexins in the Plasmopara viticola-grapevine interaction. Physiol Mol Plant Pathol. 1989; 34: 189-202.

[50]

Yu CKY, Shih C-H, Chu IK et al. Accumulation of trans-piceid in sorghum seedlings infected with Colletotrichum sublineolum . Phytochemistry. 2008; 69: 700-6.

[51]

Vannozzi A, Dry IB, Fasoli M et al. Genome-wide analysis of the grapevine stilbene synthase multigenic family: genomic organization and expression profiles upon biotic and abiotic stresses. BMC Plant Biol. 2012; 12: 130.

[52]

Höll J, Vannozzi A, Czemmel S et al. The R2R3-MYB transcription factors MYB14 and MYB15 regulate stilbene biosynthesis in Vitis vinifera . Plant Cell. 2013; 25: 4135-49.

[53]

Wang L, Wang Y . Transcription factor VqERF114 regulates stilbene synthesis in Chinese wild Vitis quinquangularis by interacting with VqMYB35. Plant Cell Rep. 2019; 38: 1347-60.

[54]

Onkokesung N, Reichelt M, van Doorn A et al. Differential costs of two distinct resistance mechanisms induced by different herbivore species in Arabidopsis . Plant Physiol. 2016; 170: 891-906.

[55]

Skadhauge B, Thomsen KK, von Wettstein D . The role of the barley testa layer and its flavonoid content in resistance to Fusarium infections. Hereditas. 1997; 126: 147-60.

[56]

Gatto MA, Ippolito A, Sergio L et al. Activity of extracts from wild edible herbs against postharvest fungal diseases of fruit and vegetables. Postharvest Biol Technol. 2011; 61: 72-82.

[57]

Zhang Q, Yang F, Tong H et al. Plant flavonoids enhance the tolerance to thiamethoxam and flupyradifurone in whitefly Bemisia tabaci (Hemiptera: Aleyrodidae) . Pestic Biochem Physiol. 2021; 171: 104744.

[58]

Cheng H, Mou Z, Wang W et al. Chitosan-catechin coating as an antifungal and preservable agent for postharvest satsuma oranges. J Food Biochem. 2019; 43: e12779.

[59]

Hammerbacher A, Raguschke B, Wright LP et al. Gallocatechin biosynthesis via a flavonoid 3,5-hydroxylase is a defense response in Norway spruce against infection by the bark beetle-associated sap-staining fungus Endoconidiophora polonica . Phytochemistry. 2018; 148: 78-86.

[60]

Hong G, Wang J, Hochstetter D et al. Epigallocatechin-3-gallate functions as a physiological regulator by modulating the jasmonic acid pathway. Physiol Plant. 2015; 153: 432-9.

[61]

Yuan L, Wang L, Han Z et al. Molecular cloning and characterization of PtrLAR3, a gene encoding leucoanthocyanidin reductase from Populus trichocarpa, and its constitutive expression enhances fungal resistance in transgenic plants. J Exp Bot. 2012; 63: 2513-24.

[62]

Wang L, Ran L, Hou Y et al. The transcription factor MYB115 contributes to the regulation of proanthocyanidin biosynthesis and enhances fungal resistance in poplar. New Phytol. 2017; 215: 351-67.

[63]

Deluc L, Bogs J, Walker AR et al. The transcription factor VvMYB5b contributes to the regulation of anthocyanin and proanthocyanidin biosynthesis in developing grape berries. Plant Physiol. 2008; 147: 2041-53.

[64]

Huang Y-F, Vialet S, Guiraud J-L et al. A negative MYB regulator of proanthocyanidin accumulation, identified through expression quantitative locus mapping in the grape berry. New Phytol. 2014; 201: 795-809.

[65]

Shan X, Li Y, Yang S et al. A functional homologue of Arabidopsis TTG1 from freesia interacts with bHLH proteins to regulate anthocyanin and proanthocyanidin biosynthesis in both Freesia hybrida and Arabidopsis thaliana . Plant Physiol Biochem. 2019; 141: 60-72.

[66]

Mao X, Cai T, Olyarchuk J et al. Automated genome annotation and pathway identification using the KEGG Orthology (KO) as a controlled vocabulary. Bioinformatics. 2005; 21: 3787-3793.

[67]

Chen W, Gong L, Guo Z et al. A novel integrated method for large-scale detection, identification, and quantification of widely targeted metabolites: application in the study of rice metabolomics. Mol Plant. 2013; 6: 1769-1780.

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