Phytoplasma effector Zaofeng6 induces shoot proliferation by decreasing the expression of ZjTCP7 in Ziziphus jujuba

Peng Chen , Lichuan Chen , Xia Ye , Bin Tan , Xianbo Zheng , Jun Cheng , Wei Wang , Qiqi Yang , Yu Zhang , Jidong Li , Jiancan Feng

Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) : uhab032

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Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) :uhab032 DOI: 10.1093/hr/uhab032
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Phytoplasma effector Zaofeng6 induces shoot proliferation by decreasing the expression of ZjTCP7 in Ziziphus jujuba
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Abstract

The jujube witches’ broom (JWB) phytoplasma is associated with witches’ broom, dwarfism, and smaller leaves in jujube, resulting in yield losses. In this study, eight putative JWB effector proteins were identified from potential mobile units of the JWB genome. Among them, Zaofeng6 induced witches’ broom symptoms in Arabidopsis and jujube. Zaofeng6-overexpressing Arabidopsis and unrooted jujube transformants displayed witches’ broom-like shoot proliferation. Transient expression of Zaofeng6 induced hypersensitive response like cell death and expression of hypersensitive response marker genes, like harpin-induced gene 1 (H1N1), and the pathogenesis-related genes PR1, PR2, and PR3 in transformed Nicotiana benthamiana leaves, suggesting that Zaofeng6 could be a virulence effector. Yeast two-hybrid library screening and bimolecular fluorescence complementation confirmed that Zaofeng6 interacts with ZjTCP7 through its first two α-helix domains in the cell nuclei. ZjTCP7 mRNA and protein abundance decreased in Zaofeng6 transgenic jujube seedlings. The expression of some genes in the strigolactone signaling pathway (ZjCCD7, ZjCCD8, and CYP711A1) were down-regulated in jujube shoots overexpressing Zaofeng6 and in zjtcp7 CRISPR/Cas9 mutants. Zaofeng6 induces shoot proliferation through decreased expression of ZjTCP7 at the transcriptional and translational levels.

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Peng Chen, Lichuan Chen, Xia Ye, Bin Tan, Xianbo Zheng, Jun Cheng, Wei Wang, Qiqi Yang, Yu Zhang, Jidong Li, Jiancan Feng. Phytoplasma effector Zaofeng6 induces shoot proliferation by decreasing the expression of ZjTCP7 in Ziziphus jujuba. Horticulture Research, 2022, 9 (1) : uhab032 DOI:10.1093/hr/uhab032

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References

[1]

Bertaccini A, Duduk B, Paltrinieri S et al. Phytoplasmas and phytoplasma disease: a severe threat to agriculture. Am J Plant Sci. 2014; 5: 1763-88.

[2]

Namba S . Molecular and biological properties of phytoplasmas. Proc Jpn Acad Ser B. 2019; 95: 401-18.

[3]

Kumari S, Nagendran K, Bahadur Rai A et al. Global status of phytoplasma disease in vegetable crops. Front Microbiol. 2019; 10: 1349.

[4]

Dickinson M. Mobile units of DNA in phytoplasma genomes. Mol Microbiol. 2010; 77: 1351-3.

[5]

Tomkins M, Kliot A, Marée AF et al. A multi-layered mechanistic modelling approach to understand how effector genes extend beyond phytoplasma to modulate plant hosts, insect vectors and the environment. Curr Opin Plant Biol. 2018; 44: 39-48.

[6]

Garcion C, Beven L, Foissac X . Comparison of current methods for signal peptide prediction in phytoplasmas. Front Microbiol. 2021; 12: 661524.

[7]

Sugio A, Hogenhout AS . The genome biology of phytoplasma: modulators of plants and insects. Curr Opin Microbiol. 2012; 15: 247-54.

[8]

Bai X, Correa VR, Toruño TY et al. AY-WB phytoplasma secretes a protein that targets plant cell nuclei. Mol Plant-Microbe Interact. 2009; 22: 18-30.

[9]

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. 2011a; 108: E1254-63.

[10]

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.

[11]

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.

[12]

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.

[13]

Maejima K, Iwai R, Himeno M et al. Recognition of floral homeotic MADS domain transcription factors by a phytoplasmal effector, phyllogen, induces phyllody. Plant J. 2014; 78: 541-54.

[14]

Iwabuchi N, Kitazawa Y, Maejima K et al. Functional variation in phyllogen, a phyllody-inducing phytoplasma effector family, attributable to a single amino acid polymorphism. Mol Plant Pathol. 2020; 21: 1322-36.

[15]

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. 2009; 106: 6416-21.

[16]

Sugawara K, Honma Y, Komatsu K et al. The alteration of plant morphology by small peptides released from the proteolytic processing of the bacterial peptide TENGU. Plant Physiol. 2013; 162: 2005-14.

[17]

Yao S. Past, present, and future of jujubes-Chinese dates in the United States. HortScience. 2013; 38: 672-80.

[18]

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.

[19]

Liu M. The challenges and countermeasures of jujube industry during transition period. China Fruits. 2018; 1: 1-4.

[20]

Zhu S, Bartoszyk I, Gundersen-Rindal D et al. Characterization of the phytoplasmas associated with cherry lethal yellows and jujube witches’-broom diseases in China. Acta Hortic. 1998; 472: 701-14.

[21]

Liu M, Qiao Y, Zhao J et al. Jujube Witches’ Broom Disease . Beijing: China Agriculture Press; 2009.

[22]

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.

[23]

Bertaccini A . Phytoplasmas: diversity, taxonomy, and epidemiology. Front Biosci. 2007; 12: 673-89.

[24]

Zhao J et al. The variations of endogenous hormones in Chinese jujube infected with witches’ broom disease. Sci Agric Sin. 2006; 39: 2255-60.

[25]

Liu YQ et al. Effect of jujube witches’ broom (JWB) phytoplasma on the chlorophyll and several protective enzymes in jujube trees. Acta Agriculturae Boreali Sinica. 2012; 27: 213-7.

[26]

Liu ZG, Zhao J, Liu MJ . Photosynthetic response to phytoplasma infection in Chinese jujube. Plant Physiol Biochem. 2016; 105: 12-20.

[27]

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.

[28]

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.

[29]

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.

[30]

Chen P, Li J, Ye X et al. Genome-wide identification of Ziziphus jujuba TCP transcription factors and their expression in response to infection with jujube witches’ broom phytoplasma. Acta Physiol Plant. 2019; 41: 86.

[31]

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. https://doi.org/10.1007/s13562-021-00670-4.

[32]

Shao FJ . Genome-wide identification and characterization of the SPL gene family in Ziziphus jujuba . Gene. 2017; 627: 315-21.

[33]

Zhang Y . Genome-wide analysis of the bZIP gene family in Chinese jujube (Ziziphus jujuba Mill.) . BMC Genomics. 2020; 21: 483.

[34]

Liu ZG . Genome-wide identification of MAPKKK genes and their response to phytoplasma infection in Chinese jujube (Ziziphus jujuba Mill.) . BMC Genomics. 2020; 21: 142.

[35]

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.

[36]

Dai L, Jialuo G, Yuhuan F et al. Leafhopper species screening of potential vector transmitting jujube witches’-broom phytoplasma in Beijing. Journal of Beijing University of Agriculture. 2019; 34: 59-65.

[37]

Hao S, Chen YQ, Wang JZ et al. Multiplex-PCR for identification of two Hishimonus species (Hemiptera: Cicadellidae) in jujube orchards and detection of jujube witches’ broom (JWB) phytoplasma in their bodies. Acta Entomol Sin. 2015; 58: 264-70.

[38]

Kusunoki M, Shiomi T, Kobayashi M et al. A leafhopper (Hishimonus sellatus) transmits phylogenetically distant phytoplasmas: Rhus yellows and Hovenia witches’ broom phytoplasma . J Gen Plant Pathol. 2002; 68: 147-54.

[39]

Ku C, Lo W-S, Kuo C-H et al. Horizontal transfer of potential mobile units in phytoplasmas. Mob Genet Elements. 2013; 3: e26145.

[40]

Cui H, Tsuda K, Parker JE et al. Effector-triggered immunity: from pathogen perception to robust defense. Annu Rev Plant Biol. 2015; 66: 487-511.

[41]

Wang N, Li Y, Chen W et al. Identification of wheat blue dwarf phytoplasma effectors targeting plant proliferation and defence responses. Plant Pathol. 2018; 67: 603-9.

[42]

Rameau C, Bertheloot J, Leduc N et al. Multiple pathways regulate shoot branching. Front Plant Sci. 2014; 5: 741.

[43]

Shang Y, Yuan L, Di Z et al. A CYC/TB1-type TCP transcription factor controls spikelet meristem identity in barley. J Exp Bot. 2020; 71: 7118-31.

[44]

Muhr M, Paulat M, Awwanah M et al. CRISPR/Cas9-mediated knockout of Populus BRANCHED1 and BRANCHED2 orthologs reveals a major function in bud outgrowth control . Tree Physiol. 2018; 10: 1588-97.

[45]

Feng J, Yu XM, Shang L et al. Factors influencing efficiency of shoot regeneration in Ziziphus jujuba Mill. ‘Huizao’. Plant Cell Tissue Organ Cult. 2009; 101: 111-7.

[46]

Petersen TN, Brunak S, von Heijne G et al. SignalP 4.0 discriminating signal peptides from transmembrane regions. Nat Methods. 2011; 8: 785-6.

[47]

Krogh A, Larsson B, von Heijne G et al. Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J Mol Biol. 2001; 305: 567-80.

[48]

Bai X, Zhang J, Ewing A et al. Living with genome in stability: the adaptation of phytoplasmas to diverse environments of their insect and plant hosts. J Bacteriol. 2006; 188: 3682-96.

[49]

Clough SJ, Bent AF . Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana . Plant J. 2010; 16: 735-43.

[50]

Concordet JP, Maximilian, h . CRISPOR: intuitive guide selection for CRISPR/Cas9 genome editing experiments and screens. Nucleic Acids Res. 2018; W1: W242-5.

[51]

Abid K, Fazaa B, Hadouchi CH et al. Differential expression of Bcl-2, Bax, and CD95 in DNA repair-proficient and DNA repair-deficient basal cell carcinoma patients. Int J Dermatol. 2006; 45: 1482-5.

[52]

Cowell IG. Yeast two-hybrid library screening. In: Cowell IG, Austin CA (eds.). cDNA Library Protocols (Methods in Molecular Biology), vol. 69. Totowa, NJ: Humana Press, 1997, 185-202.

[53]

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

[54]

Chen JH, Yang R, Wang YP et al. Expression data analysis to identify key target genes in visceral fat tissue associated with obstructive sleep apnea. Eur Rev Med Pharmacol Sci. 2015; 19: 4293-9.

[55]

Sun M, Shi M, Wang Y et al. The biosynthesis of phenolic acids is positively regulated by the JA-responsive transcription factor ERF115 in Salvia miltiorrhiza . J Exp Bot. 2019; 70: 243-54.

[56]

Gundersen DE, Lee IM . Ultrasensitive detection of phytoplasmas by nested-PCR assays using two universal primer pairs. Phytopathol Mediterr. 1996; 35: 144-51.

[57]

Lee IM, Bertaccini A, Vibio M et al. Detection of multiple phytoplasmas in perennial fruit trees with decline symptoms in Italy. Phytopathology. 1995; 85: 728-35.

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