Jujube witches’ broom phytoplasmas inhibit ZjBRC1-mediated abscisic acid metabolism to induce shoot proliferation

Fuli Ma , Shanqi Zhang , Yu Yao , Mengting Chen , Ning Zhang , Mingsheng Deng , Wei Chen , Chi Ma , Xinyue Zhang , Chenglong Guo , Xiang Huang , Zhenyuan Zhang , Yamei Li , Tingyi Li , Junyong Zhou , Qibao Sun , Jun Sun

Horticulture Research ›› 2023, Vol. 10 ›› Issue (9) : 148

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Horticulture Research ›› 2023, Vol. 10 ›› Issue (9) :148 DOI: 10.1093/hr/uhad148
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Jujube witches’ broom phytoplasmas inhibit ZjBRC1-mediated abscisic acid metabolism to induce shoot proliferation
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Abstract

Jujube witches’ broom (JWB) phytoplasmas parasitize the sieve tubes of diseased phloem and cause an excessive proliferation of axillary shoots from dormant lateral buds to favour their transmission. In previous research, two JWB effectors, SJP1 and SJP2, were identified to induce lateral bud outgrowth by disrupting ZjBRC1-mediated auxin flux. However, the pathogenesis of JWB disease remains largely unknown. Here, tissue-specific transcriptional reprogramming was examined to gain insight into the genetic mechanisms acting inside jujube lateral buds under JWB phytoplasma infection. JWB phytoplasmas modulated a series of plant signalling networks involved in lateral bud development and defence, including auxin, abscisic acid (ABA), ethylene, jasmonic acid, and salicylic acid. JWB-induced bud outgrowth was accompanied by downregulation of ABA synthesis within lateral buds. ABA application rescued the bushy appearances of transgenic Arabidopsis overexpressing SJP1 and SJP2 in Col-0 and ZjBRC1 in the brc1-2 mutant. Furthermore, the expression of ZjBRC1 and ABA-related genes ZjHB40 and ZjNCED3 was negatively correlated with lateral main bud outgrowth in decapitated healthy jujube. Molecular evidence showed that ZjBRC1 interacted with ZjBRC2 via its N-terminus to activate ZjHB40 and ZjNCED3 expression and ABA accumulation in transgenic jujube calli. In addition, ZjBRC1 widely regulated differentially expressed genes related to ABA homeostasis and ABA signalling, especially by binding to and suppressing ABA receptors. Therefore, these results suggest that JWB phytoplasmas hijack the ZjBRC1-mediated ABA pathways to stimulate lateral bud outgrowth and expansion, providing a strategy to engineer plants resistant to JWB phytoplasma disease and regulate woody plant architecture to promote crop yield and quality.

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Fuli Ma, Shanqi Zhang, Yu Yao, Mengting Chen, Ning Zhang, Mingsheng Deng, Wei Chen, Chi Ma, Xinyue Zhang, Chenglong Guo, Xiang Huang, Zhenyuan Zhang, Yamei Li, Tingyi Li, Junyong Zhou, Qibao Sun, Jun Sun. Jujube witches’ broom phytoplasmas inhibit ZjBRC1-mediated abscisic acid metabolism to induce shoot proliferation. Horticulture Research, 2023, 10 (9) : 148 DOI:10.1093/hr/uhad148

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Acknowledgements

This work was supported by the National Natural Science Foundation of China (31971687 and 32002007), the Anhui Province Key Research and Development Program (202004a06020008), the Natural Science Foundation of Anhui Province (2008085QC127), and the Natural Science Foundation of Anhui Provincial Department of Education (KJ2019A0186).

Author contributions

J.S., Q.S., and F.M. planned and designed the research; S.Z., F.M., M.C., N.Z., M.D., and J.Z. performed the experiments; Y.Y., Y.L., C.M., X.Z., C.G., X.H., Z.Z., W.C., and T.L. conducted the transformation; J.S., Q.S., and F.M. analysed the data; F.M. wrote the manuscript; and J.S. and Q.S. revised the manuscript.

Data availability

All relevant data generated or analyzed are included in the manuscript and the supporting materials.

Conflict of interest

The authors declare that there are no conflicts of interest.

References

[1]

Guo M, Zhang Z, Li S et al. Genomic analyses of diverse wild and cultivated accessions provide insights into the evolutionary history of jujube. Plant Biotechnol J. 2021; 19: 517-31

[2]

Liu M, Wang J, Wang L et al. The historical and current research progress on jujube - a superfruit for the future. Hortic Res. 2020; 7: 119

[3]

Sobhani Z, Nikoofal-Sahlabadi S, Amiri MS et al. Therapeutic effects of Ziziphus jujuba Mill. fruit in traditional and modern medicine: a review. Med Chem. 2020; 16: 1069-88

[4]

Rashwan AK, Karim N, Shishir MRI et al. Jujube fruit: a potential nutritious fruit for the development of functional food products. J Funct Foods. 2020; 75: 104205

[5]

Zhao J, Liu Z, Liu M . The resistance of jujube trees to jujube witches’ broom disease in China. In: Oliviere CY, Dumonceaux TJ, Pérez-López E (eds). Sustainable Management of Phytoplasma Diseases in Crops Grown in the Tropical Belt. Cham: Springer, 2019, 219-32.

[6]

No authors listed. Studies on the pathogens of Chinese jujube witches’ broom disease. I. Viruslike particles associated with jujube witches’ broom disease. Science in China, Ser A. 1974; 12: 681-7

[7]

Zhou Z, Sun J, Zhou J et al. Homology analysis of 16S r DNA sequences from jujube witches’ broom in Anhui. Province J Anhui Agric Univ. 2014; 4: 150-4

[8]

Jung HY, Sawayanagi T, Kakizawa S et al. ‘Candidatus Phytoplasma ziziphi’, a novel phytoplasma taxon associated with jujube witches’-broom disease. Int J Syst Evol Microbiol. 2003; 53: 1037-41

[9]

Wang J, Song L, Jiao Q et al. Comparative genome analysis of jujube witches’-broom phytoplasma, an obligate pathogen that causes jujube witches’-broom disease. BMC Genomics. 2018; 19: 689

[10]

Jin Z, Mengjun L, Junyi Z . Distribution and year-round concentration variation of jujube witches’ broom (JWB) phytoplasma in the plant of Chinese jujube. Scientia Silvae Sinicae. 2006; 42: 144

[11]

Sugio A, MacLean AM, Kingdom HN et al. Diverse targets of phytoplasmal effectors: from plant development to defense against insects. Annu Rev Phytopathol. 2011; 49: 175-95

[12]

MacLean AM, Orlovskis Z, Kowitwanich K et al. Phytoplasma effector SAP54 hijacks plant reproduction by degrading MADS-box proteins and promotes insect colonization in a RAD23-dependent manner. PLoS Biol. 2014; 12: e1001835

[13]

Huang W, MacLean AM, Sugio A et al. Parasitic modulation of host development by ubiquitin-independent protein degradation. Cell. 2021; 184: 5201-5214.e12

[14]

Al-Subhi AM, Al-Sadi AM, Al-Yahyai RA et al. Witches’ broom disease of lime contributes to phytoplasma epidemics and attracts insect vectors. Plant Dis. 2021; 105: 2637-48

[15]

Xue C, Liu Z, Dai L et al. Changing host photosynthetic, carbohydrate, and energy metabolisms play important roles in phytoplasma infection. Phytopathology. 2018; 108: 1067-77

[16]

Liu Z, Zhao J, Liu M . Photosynthetic responses to phytoplasma infection in Chinese jujube. Plant Physiol Biochem. 2016; 105: 12-20

[17]

Song L, Meinhardt LW, Bailey B et al. Genetic improvement of Chinese jujube for disease resistances: status, knowledge gaps and research needs. Crop Breeding, Genetics and Genomics. 2019; 1: e190015

[18]

Wang R, Mou H, Gao X et al. Cryopreservation for eradication of jujube witches’ broom phytoplasma from Chinese jujube (Ziziphus jujuba). Ann Appl Biol. 2015; 166: 218-28

[19]

Ye X, Wang H, Chen P et al. Combination of iTRAQ proteomics and RNA-seq transcriptomics reveals multiple levels of regulation in phytoplasma-infected Ziziphus jujuba Mill. Hortic Res. 2017; 4: 17080

[20]

Wang H, Ye X, Li J et al. Transcriptome profiling analysis revealed co-regulation of multiple pathways in jujube during infection by ‘Candidatus Phytoplasma ziziphi’. Gene. 2018; 665: 82-95

[21]

Wang H, Ye X, Li J et al. Combination of iTRAQ proteomics and RNA-seq transcriptomics reveals jasmonate-related-metabolisms central regulation during the process of jujube witches’ broom recovery by tetracycline treatment. Sci Hortic. 2019; 243: 197-206

[22]

Sugio A, Kingdom HN, MacLean AM et al. Phytoplasma protein effector SAP11 enhances insect vector reproduction by manipulating plant development and defense hormone biosynthesis. Proc Natl Acad Sci USA. 2011; 108: E1254-63

[23]

Sugio A, MacLean AM, Hogenhout SA . The small phytoplasma virulence effector SAP11 contains distinct domains required for nuclear targeting and CIN-TCP binding and destabilization. New Phytol. 2014; 202: 838-48

[24]

Janik K, Mithöfer A, Raffeiner M et al. An effector of apple proliferation phytoplasma targets TCP transcription factors - a generalized virulence strategy of phytoplasma? Mol Plant Pathol. 2017; 18: 435-42

[25]

Wang N, Yang H, Yin Z et al. Phytoplasma effector SWP1 induces witches’ broom symptom by destabilizing the TCP transcription factor BRANCHED1. Mol Plant Pathol. 2018; 19: 2623-34

[26]

Chang SH, Tan CM, Wu C et al. Alterations of plant architecture and phase transition by the phytoplasma virulence factor SAP11. J Exp Bot. 2018; 69: 5389-401

[27]

Pecher P, Moro G, Canale MC et al. Phytoplasma SAP11 effector destabilization of TCP transcription factors differentially impact development and defence of Arabidopsis versus maize. PLoS Pathog. 2019; 15: e1008035

[28]

MacLean AM, Sugio A, Makarova OV et al. Phytoplasma effector SAP54 induces indeterminate leaf-like flower development in Arabidopsis plants. Plant Physiol. 2011; 157: 831-41

[29]

Cao Y, Sun G, Zhai X et al. Genomic insights into the fast growth of paulownias and the formation of Paulownia witches’ broom. Mol Plant. 2021; 14: 1668-82

[30]

Zhou J, Ma F, Yao Y et al. Jujube witches’ broom phytoplasma effectors SJP1 and SJP2 induce lateral bud outgrowth by repressing the ZjBRC1-controlled auxin efflux channel. Plant Cell Environ. 2021; 44: 3257-72

[31]

Wang L, Wang B, Yu H et al. Transcriptional regulation of strigolactone signalling in Arabidopsis. Nature. 2020; 583: 277-81

[32]

Zhang C, Fan L, Le BH et al. Regulation of ARGONAUTE10 expression enables temporal and spatial precision in axillary meristem initiation in Arabidopsis. Dev Cell. 2020; 55: 603-616.e5

[33]

Singh RK, Maurya JP, Azeez A et al. A genetic network mediating the control of bud break in hybrid aspen. Nat Commun. 2018; 9: 4173

[34]

Ranocha P, Dima O, Nagy R et al. Arabidopsis WAT1 is a vacuolar auxin transport facilitator required for auxin homoeostasis. Nat Commun. 2013; 4: 2625

[35]

González-Grandío E, Pajoro A, Franco-Zorrilla JM et al. Abscisic acid signaling is controlled by a BRANCHED1/HD-ZIP I cascade in Arabidopsis axillary buds. Proc Natl Acad Sci USA. 2017; 114: E245-54

[36]

González-Grandío E, Poza-Carrión C, Sorzano COS et al. BRANCHED1 promotes axillary bud dormancy in response to shade in Arabidopsis. Plant Cell. 2013; 25: 834-50

[37]

Wang B, Smith SM, Li J . Genetic regulation of shoot architecture. Annu Rev Plant Biol. 2018; 69: 437-68

[38]

Fichtner F, Barbier FF, Kerr SC et al. Plasticity of bud outgrowth varies at cauline and rosette nodes in Arabidopsis thaliana. Plant Physiol. 2022; 188: 1586-603

[39]

Hernández F, Legua P, Melgarejo P et al. Phenological growth stages of jujube tree (Ziziphus jujube): codification and description according to the BBCH scale. Ann Appl Biol. 2015; 166: 136-42

[40]

Seemüller E, Schneider B . ‘Candidatus Phytoplasma Mali’, ‘Candidatus Phytoplasma pyri’ and ‘Candidatus Phytoplasma prunorum’, the causal agents of apple proliferation, pear decline and European stone fruit yellows, respectively. Int J Syst Evol Microbiol. 2004; 54: 1217-26

[41]

Musetti R, Buxa SV, De Marco F et al. Phytoplasma-triggered Ca 2+ influx is involved in sieve-tube blockage . Mol Plant-Microbe Interact. 2013; 26: 379-86

[42]

Li J, Chen L, Chen P et al. Genome-wide identification and expression of the lipoxygenase gene family in jujube (Ziziphus jujuba) in response to phytoplasma infection. J Plant Biochem Biotechnol. 2022; 31: 139-53

[43]

Liu Z, Wang L, Xue C et al. Genome-wide identification of MAPKKK genes and their responses to phytoplasma infection in Chinese jujube (Ziziphus jujuba Mill.). BMC Genomics. 2020; 21: 142

[44]

Liu Z, Zhang L, Xue C et al. Genome-wide identification and analysis of MAPK and MAPKK gene family in Chinese jujube (Ziziphus jujuba mill.). BMC Genomics. 2017; 18: 855

[45]

Hoshi A, Oshima K, Kakizawa S et al. A unique virulence factor for proliferation and dwarfism in plants identified from a phytopathogenic bacterium. Proc Natl Acad Sci USA. 2009; 106: 6416-21

[46]

Minato N, Himeno M, Hoshi A et al. The phytoplasmal virulence factor TENGU causes plant sterility by downregulating of the jasmonic acid and auxin pathways. Sci Rep. 2014; 4: 7399-405

[47]

Ophir R, Pang X, Halaly T et al. Gene-expression profiling of grape bud response to two alternative dormancy-release stimuli expose possible links between impaired mitochondrial activity, hypoxia, ethylene-ABA interplay and cell enlargement. Plant Mol Biol. 2009; 71: 403-23

[48]

Holalu SV, Finlayson SA . The ratio of red light to far red light alters Arabidopsis axillary bud growth and abscisic acid signalling before stem auxin changes. J Exp Bot. 2017; 68: 943-52

[49]

Shi Z, Halaly-Basha T, Zheng C et al. Transient induction of a subset of ethylene biosynthesis genes is potentially involved in regulation of grapevine bud dormancy release. Plant Mol Biol. 2018; 98: 507-23

[50]

Reddy SK, Holalu SV, Casal JJ et al. Abscisic acid regulates axillary bud outgrowth responses to the ratio of red to far-red light. Plant Physiol. 2013; 163: 1047-58

[51]

Yao C, Finlayson SA . Abscisic acid is a general negative regulator of Arabidopsis axillary bud growth. Plant Physiol. 2015; 169: 611-26

[52]

Yang Q, Yang B, Li J et al. ABA-responsive ABRE-BINDING FACTOR3 activates DAM3 expression to promote bud dormancy in Asian pear. Plant Cell Environ. 2020; 43: 1360-75

[53]

Tuan PA, Bai S, Saito T et al. Dormancy-associated MADS-box (DAM) and the abscisic acid pathway regulate pear endodormancy through a feedback mechanism. Plant Cell Physiol. 2017; 58: 1378-90

[54]

Zheng C, Acheampong AK, Shi Z et al. Abscisic acid catabolism enhances dormancy release of grapevine buds. Plant Cell Environ. 2018; 41: 2490-503

[55]

Tylewicz S, Petterle A, Marttila S et al. Photoperiodic control of seasonal growth is mediated by ABA acting on cell-cell communication. Science. 2018; 360: 212-5

[56]

Dong Z, Xiao Y, Govindarajulu R et al. The regulatory landscape of a core maize domestication module controlling bud dormancy and growth repression. Nat Commun. 2019; 10: 3810

[57]

Liu R, Finlayson SA . Sorghum tiller bud growth is repressed by contact with the overlying leaf. Plant Cell Environ. 2019; 42: 2120-32

[58]

Domagalska MA, Leyser O . Signal integration in the control of shoot branching. Nat Rev Mol Cell Biol. 2011; 12: 211-21

[59]

Deng M, Ma F, Zhang X et al. Genome-wide identification of jujube witches’ broom phytoplasma effectors revealed the role of SJP3 in inducing phyllody. Sci Hortic. 2021; 290: 110548

[60]

Nicolas M, Rodríguez-Buey ML, Franco-Zorrilla JM et al. A recently evolved alternative splice site in the BRANCHED1a gene controls potato plant architecture. Curr Biol. 2015; 25: 1799-809

[61]

Niwa M, Daimon Y, Kurotani Ki et al. BRANCHED1 interacts with FLOWERING LOCUS T to repress the floral transition of the axillary meristems in Arabidopsis. Plant Cell. 2013; 25: 1228-42

[62]

Maurya JP, Singh RK, Miskolczi PC et al. Branching regulator BRC1 mediates photoperiodic control of seasonal growth in hybrid aspen. Curr Biol. 2020; 30: 122-126.e2

[63]

Li D, Zhang H, Mou M et al. Arabidopsis class II TCP transcription factors integrate with the FT-FD module to control flowering. Plant Physiol. 2019; 181: 97-111

[64]

Ma F, Huang J, Yang J et al. Identification, expression and miRNA targeting of auxin response factor genes related to phyllody in the witches’ broom disease of jujube. Gene. 2020; 746: 144656

[65]

Clough SJ, Bent AF . Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. 1998; 16: 735-43

[66]

Aguilar-Martínez JA, Poza-Carrión C, Cubas P . Arabidopsis BRANCHED1 acts as an integrator of branching signals within axillary buds. Plant Cell. 2007; 19: 458-72

[67]

Ma F, Wang L, Wang Y . Ectopic expression of VpSTS29, a stilbene synthase gene from Vitis pseudoreticulata, indicates STS presence in cytosolic oil bodies. Planta. 2018; 248: 89-103

[68]

Liu MJ, Zhao J, Cai QL et al. The complex jujube genome provides insights into fruit tree biology. Nat Commun. 2014; 5: 5315

[69]

Pertea M, Pertea GM, Antonescu CM et al. StringTie enables improved reconstruction of a transcriptome from RNA-seq reads. Nat Biotechnol. 2015; 33: 290-5

[70]

Chen C, Chen H, Zhang Y et al. TBtools: an integrative toolkit developed for interactive analyses of big biological data. Mol Plant. 2020; 13: 1194-202

[71]

Hiratsu K, Matsui K, Koyama T et al. Dominant repression of target genes by chimeric repressors that include the EAR motif, a repression domain, in Arabidopsis. Plant J. 2003; 34: 733-9

[72]

Floková K, Tarkowská D, Miersch O et al. UHPLC-MS/MS based target profiling of stress-induced phytohormones. Phytochemistry. 2014; 105: 147-57

[73]

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

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