PpMYB123-mediated proanthocyanidin accumulation alleviates bacterial spot disease in peach

Lei Zhao , Di Ai , Zhaoyang Li , Miaoyi Li , Chaoxi Luo , Qian Peng , Yuepeng Han , Jian-Ping An

Horticulture Research ›› 2026, Vol. 13 ›› Issue (5) : 32

PDF (2054KB)
Horticulture Research ›› 2026, Vol. 13 ›› Issue (5) :32 DOI: 10.1093/hr/uhag032
Articles
research-article
PpMYB123-mediated proanthocyanidin accumulation alleviates bacterial spot disease in peach
Author information +
History +
PDF (2054KB)

Abstract

Bacterial spot (BS) disease significantly impairs vigor, fruit quality, and yield in peach trees. However, research on this disease remains limited. In this study, peach leaves and fruits were inoculated with the pathogen isolated from infected leaves, triggering a robust accumulation of proanthocyanidins (PA) in both tissues. Further investigation revealed that pathogen inoculation promoted PA accumulation by upregulating PpMYB123, which transactivated the core PA biosynthetic genes PpANR and PpLAR. Notably, the E3 ubiquitin ligase PpPUB23 negatively regulated PpMYB123. However, its transcript levels were significantly suppressed following inoculation, thereby stabilizing PpMYB123 and enhancing PA production. PA conferred dual protection by scavenging excess reactive oxygen species (ROS) and suppressing pathogen growth. Our findings provide molecular evidence for PA-mediated defense against BS disease in peach.

Cite this article

Download citation ▾
Lei Zhao, Di Ai, Zhaoyang Li, Miaoyi Li, Chaoxi Luo, Qian Peng, Yuepeng Han, Jian-Ping An. PpMYB123-mediated proanthocyanidin accumulation alleviates bacterial spot disease in peach. Horticulture Research, 2026, 13 (5) : 32 DOI:10.1093/hr/uhag032

登录浏览全文

4963

注册一个新账户 忘记密码

Acknowledgements

This project was supported by funds received from National Natural Science Foundation of China (32302497), the China Agriculture Research System (grant CARS-30) and the Wuhan Botanical Garden Scientific Research Support Project (E3559901).

Author contributions

J.-P.A. and L.Z. planned and designed the experiments. L.Z., D.A., Z.L. and M.L. performed the experiments. C.L. and Q.P. collected experiment samples. D.A., and Z.L. performed the sequence analysis. L.Z. wrote the paper. J.-P.A. and Y.H. revised the manuscript.

Data availability

All data can be found online in the main text and supporting information materials.

Conflicts of interest statement

The authors declare no competing interests.

Supplementary material

Supplementary material is available at Horticulture Research online.

References

[1]

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

[2]

Dey N, Roy UK, Aditya M, et al. Defensive strategies of ROS in programmed cell death associated with hypertensive response in plant pathogenesis. Ann Syst Biol . 2020; 3: 001-9

[3]

Liu Y, Zhang H . Reactive oxygen species and nitric oxide as mediators in plant hypersensitive response and stomatal closure. Plant Signal Behav . 2021; 16: 1985860

[4]

Nanda AK, Andrio E, Marino D, et al. Reactive oxygen species during plant-microorganism early interactions. J Integr Plant Biol. 2010; 52: 195-204

[5]

Torres MA, Jones JDG, Dangl JL . Reactive oxygen species signaling in response to pathogens. Plant Physiol . 2006; 141: 373-8

[6]

Van Breusegem F, Dat JF . Reactive oxygen species in plant cell death. Plant Physiol . 2006; 141: 384-90

[7]

Xu X, Chen Y, Li B, et al. Molecular mechanisms underlying multi-level defense responses of horticultural crops to fungal pathogens. Hortic Res. 2022; 9: uhac066

[8]

Zurbriggen MD, Carrillo N, Hajirezaei MR . ROS signaling in the hypersensitive response: when, where and what for? Plant Signal Behav . 2010; 5: 393-6

[9]

Eichmann R, Richards L, Schäfer P . Hormones as go-betweens in plant microbiome assembly. Plant J . 2021; 105: 518-41

[10]

Kumar S, Korra T, Thakur R, et al. Role of plant secondary metabolites in defence and transcriptional regulation in response to biotic stress. Plant Stress . 2023; 8: 100154

[11]

Mishra S, Roychowdhury R, Ray S, et al. Salicylic acid (SA)-mediated plant immunity against biotic stresses: an insight on molecular components and signaling mechanism. Plant Stress . 2024; 11: 100427

[12]

Ngou BPM, Ding P, Jones JDG . Thirty years of resistance: zig-zag through the plant immune system. Plant Cell . 2022; 34: 1447-78

[13]

Upadhyay R, Saini R, Shukla PK, et al. Role of secondary metabolites in plant defense mechanisms: a molecular and biotechnological insights. Phytochem Rev . 2025; 24: 953-83

[14]

Cao Y, Yan X, Ran S, et al. Knockout of the lignin pathway gene BnF5H decreases the S/G lignin compositional ratio and improves Sclerotinia sclerotiorum resistance in Brassica napus . Plant Cell Environ. 2022; 45: 248-61

[15]

Xiao S, Hu Q, Shen J, et al. GhMYB4 downregulates lignin biosynthesis and enhances cotton resistance to Verticillium dahliae . Plant Cell Rep. 2021; 40: 735-51

[16]

Yang Y, He Y, Lv S, et al. The PcMYB44-mediated miR397- PcLACs module regulates defence-induced lignification in pear resistance to fungal disease . Mol Plant Pathol. 2023; 24: 1107-25

[17]

Daryanavard H, Postiglione AE, Mühlemann JK, et al. Flavonols modulate plant development, signaling, and stress responses. Curr Opin Plant Biol. 2023; 72: 102350

[18]

Li T, Wang S, Shi D, et al. Phosphate deficiency induced by infection promotes synthesis of anthracnose-resistant anthocyanin-3- O-galactoside phytoalexins in the Camellia sinensis plant . Hortic Res. 2023; 10: uhad222

[19]

Xiao J, He M, Chen P, et al. Proanthocyanidins delay the senescence of young asparagus stems by regulating antioxidant capacity and synthesis of phytochemicals. Food Chem X. 2024; 21: 101222

[20]

Yu D, Wei W, Fan Z, et al. VabHLH137 promotes proanthocyanidin and anthocyanin biosynthesis and enhances resistance to Colletotrichum gloeosporioides in grapevine . Hortic Res. 2023; 10: uhac261

[21]

Zhou LJ, Geng Z, Wang Y, et al. A novel transcription factor CmMYB012 inhibits flavone and anthocyanin biosynthesis in response to high temperatures in chrysanthemum. Hortic Res. 2021; 8: 248

[22]

Tan S, Chen S, Zhang H, et al. The PopbZIP2-PopMYB4 regulatory module enhances disease resistance in poplars by modulating proanthocyanidin accumulation. New Phytol . 2025; 246: 218-36

[23]

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

[24]

Wang Y, Wang X, Fang J, et al. VqWRKY56 interacts with VqbZIPC22 in grapevine to promote proanthocyanidin biosynthesis and increase resistance to powdery mildew. New Phytol. 2023; 237: 1856-75

[25]

Zhao T, Huang C, Li N, et al. Ubiquitin ligase VvPUB26 in grapevine promotes proanthocyanidin synthesis and resistance to powdery mildew. Plant Physiol . 2024; 195: 2891-910

[26]

Pang Y, Peel GJ, Wright E, et al. Early steps in proanthocyanidin biosynthesis in the model legume Medicago truncatula . Plant Physiol. 2007; 145: 601-15

[27]

An JP, Li R, Qu FJ, et al. R2R3-MYB transcription factor MdMYB23 is involved in the cold tolerance and proanthocyanidin accumulation in apple. Plant J . 2018; 96: 562-77

[28]

Li C, Pei J, Yan X, et al. A poplar B-box protein PtrBBX23 modulates the accumulation of anthocyanins and proanthocyanidins in response to high light. Plant Cell Environ. 2021; 44: 3015-33

[29]

Li D, Yang J, Pak S, et al. PuC3H35 confers drought tolerance by enhancing lignin and proanthocyanidin biosynthesis in the roots of Populus ussuriensis . New Phytol. 2022; 233: 390-408

[30]

An JP, Xu RR, Liu X, et al. Jasmonate induces biosynthesis of anthocyanin and proanthocyanidin in apple by mediating the JAZ1-TRB1-MYB9 complex. Plant J. 2021; 106: 1414-30

[31]

An XH, Tian Y, Chen KQ, et al. MdMYB9 and MdMYB11 are involved in the regulation of the JA-induced biosynthesis of anthocyanin and proanthocyanidin in apples . Plant Cell Physiol. 2015; 56: 650-62

[32]

Liang C, Yang B, Wei Y, et al. SA incubation induced accumulation of flavan-3-ols through activated VvANR expression in grape leaves . Sci Hortic. 2021; 287: 110269

[33]

Nesi N, Jond C, Debeaujon I, et al. The Arabidopsis TT2 gene encodes an R2R3 MYB domain protein that acts as a key determinant for proanthocyanidin accumulation in developing seed . Plant Cell. 2001; 13: 2099-114

[34]

Bogs J, Jaffé FW, Takos AM, et al. The grapevine transcription factor VvMYBPA1 regulates proanthocyanidin synthesis during fruit development. Plant Physiol. 2007; 143: 1347-61

[35]

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

[36]

Terrier N, Torregrosa L, Ageorges A, et al. Ectopic expression of VvMybPA2 promotes proanthocyanidin biosynthesis in grapevine and suggests additional targets in the pathway. Plant Physiol. 2009; 149: 1028-41

[37]

Jiang L, Yue M, Liu Y, et al. A novel R2R3-MYB transcription factor FaMYB5 positively regulates anthocyanin and proanthocyanidin biosynthesis in cultivated strawberries (Fragaria × ananassa) . Plant Biotechnol J. 2023; 21: 1140-58

[38]

Schaart JG, Dubos C, Romero De La Fuente I, et al. Identification and characterization of MYB-bHLH-WD40 regulatory complexes controlling proanthocyanidin biosynthesis in strawberry (Fragaria × ananassa) fruits . New Phytol. 2013; 197: 454-67

[39]

Zhao L, Sun J, Cai Y, et al. PpHYH is responsible for light-induced anthocyanin accumulation in fruit peel of Prunus persica . Tree Physiol. 2022; 42: 1662-77

[40]

Zhao L, Zhang Y, Sun J, et al. PpHY5 is involved in anthocyanin coloration in the peach flesh surrounding the stone . Plant J. 2023; 114: 951-64

[41]

Zhao L, Liu Y, Chen X, et al. Visible light induces the PpHYH transcription to promote anthocyanin pigmentation in peach peel . Fruit Res. 2023; 3: 25

[42]

Yan J, Cai Z, Shen Z, et al. Accumulation of proanthocyanidin monomers in two genotypes of blood-flesh peach. J Hortic Sci Biotechnol . 2017; 92: 513-20

[43]

Zhou H, Lin-Wang K, Liao L, et al. Peach MYB7 activates transcription of the proanthocyanidin pathway gene encoding leucoanthocyanidin reductase, but not anthocyanidin reductase. Front Plant Sci . 2015; 6: 908

[44]

Bi G, Hu M, Fu L, et al. The cytosolic thiol peroxidase PRXIIB is an intracellular sensor for H2O2 that regulates plant immunity through a redox relay. Nat Plants. 2022; 8: 1160-75

[45]

Tian S, Liu C, Luo F, et al. Integrated transcriptome and metabolome reveal that SlSYTA modulates ROS responses driving resistance defense in Solanum lycopersicum . Hortic Res. 2024; 11: uhae176

[46]

Wang Y, Tan J, Wu Z, et al. STAYGREEN, STAY HEALTHY: a loss-of-susceptibility mutation in the STAYGREEN gene provides durable, broad-spectrum disease resistances for over 50 years of US cucumber production . New Phytol. 2019; 221: 415-30

[47]

Wu J, Yang R, Yang Z, et al. ROS accumulation and antiviral defence control by microRNA528 in rice. Nat Plants. 2017; 3: 1-7

[48]

Ravaglia D, Espley RV, Henry-Kirk RA, et al. Transcriptional regulation of flavonoid biosynthesis in nectarine (Prunus persica) by a set of R2R3 MYB transcription factors . BMC Plant Biol. 2013; 13: 1-14

[49]

Zhou H, Peng Q, Zhao J, et al. Multiple R2R3-MYB transcription factors involved in the regulation of anthocyanin accumulation in peach flower. Front Plant Sci . 2016; 7: 1557

[50]

Ling Q, Broad W, Trösch R, et al. Ubiquitin-dependent chloroplast-associated protein degradation in plants. Science . 2019; 363: eaav4467

[51]

Liu X, Zhou Y, Chen K, et al. Phosphorylation status of CPK28 affects its ubiquitination and protein stability. New Phytol . 2023; 237: 1270-84

[52]

Potel CM, Kurzawa N, Becher I, et al. Impact of phosphorylation on thermal stability of proteins. Nat Methods. 2021; 18: 757-9

[53]

Trujillo M, Shirasu K . Ubiquitination in plant immunity. Curr Opin Plant Biol. 2010; 13: 402-8

[54]

Cho SK, Ryu MY, Song C, et al. Arabidopsis PUB22 and PUB23 are homologous U-Box E3 ubiquitin ligases that play combinatory roles in response to drought stress . Plant Cell. 2008; 20: 1899-914

[55]

Jiang MG, Yang YY, Wei W, et al. Interaction of MaERF11 with the E3 ubiquitin ligase MaRFA1 is involved in the regulation of banana starch degradation during postharvest ripening. Hortic Plant J. 2025; 11: 608-18

[56]

Park JJ, Yi J, Yoon J, et al. OsPUB15, an E3 ubiquitin ligase, functions to reduce cellular oxidative stress during seedling establishment . Plant J. 2011; 65: 194-205

[57]

Sharma M, Pandey A, Pandey GK . Role of plant U-BOX (PUB) protein in stress and development. Plant Stress. 2013; 7: 1-9

[58]

Gaona MR, Van Tuinen A, Schipper D, et al. Mutation of PUB17 in tomato leads to reduced susceptibility to necrotrophic fungi . Plant Biotechnol J. 2023; 21: 2157-9

[59]

Mou B, Zhao G, Wang J, et al. The OsCPK17-OsPUB12-OsRLCK176 module regulates immune homeostasis in rice. Plant Cell . 2024; 36: 987-1006

[60]

Zhao P, Yang H, Sun Y, et al. Targeted MYC2 stabilization confers citrus Huanglongbing resistance. Science. 2025; 388: 191-8

[61]

Han Z, Xiong D, Schneiter R, et al. The function of plant PR1 and other members of the CAP protein superfamily in plant-pathogen interactions. Mol Plant Pathol. 2023; 24: 651-68

[62]

Liu C, Liu Q, Mou Z . Redox signaling and oxidative stress in systemic acquired resistance. J Exp Bot. 2024; 75: 4535-48

[63]

Vlot AC, Sales JH, Lenk M, et al. Systemic propagation of immunity in plants. New Phytol. 2021; 229: 1234-50

[64]

Zeng HY, Wu YL, Xu LB, et al. Banana defense response against pathogens: breeding disease-resistant cultivars. Hortic Plant J. 2026; 12: 62-72

[65]

Luo M, Meng FZ, Tan Q, et al. Identification, genetic diversity, and chemical control of Xanthomonas arboricola pv. pruni in China . Plant Dis. 2022; 106: 2415-23

[66]

Socquet-Juglard D, Patocchi A, Pothier JF, et al. Evaluation of Xanthomonas arboricola pv. pruni inoculation techniques to screen for bacterial spot resistance in peach and apricot . J Plant Pathol. 2012; 94: 91-6

[67]

Zhou H, Lin-Wang K, Wang F, et al. Activator-type R2R3-MYB genes induce a repressor-type R2R3-MYB gene to balance anthocyanin and proanthocyanidin accumulation. New Phytol. 2019; 221: 1919-34

[68]

Initiative IPG, Verde I, Abbott AG, et al. The high-quality draft genome of peach (Prunus persica) identifies unique patterns of genetic diversity, domestication and genome evolution . Nat Genet. 2013; 45: 487-94

[69]

Wang K, Gao Y, Peng X, et al. Using FAM labeled DNA oligos to do RNA electrophoretic mobility shift assay. Mol Biol Rep. 2010; 37: 2871-5

[70]

An JP, Zhao L, Cao YP, et al. The SMXL8-AGL9 module mediates crosstalk between strigolactone and gibberellin to regulate strigolactone-induced anthocyanin biosynthesis in apple. Plant Cell. 2024; 36: 4404-25

PDF (2054KB)

235

Accesses

0

Citation

Detail

Sections
Recommended

/