Research Paper

Putative Phosphatase UvPsr1 Is Required for Mycelial Growth, Conidiation, Stress Response and Pathogenicity in Ustilaginonidea virens

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  • 1Key Laboratory of Three Gorges Regional Plant Genetics & Germplasm Enhancement / Biotechnology Research Center, China Three Gorges University, Yichang 443000, China;
    2State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China

#These authors contributed equally to this work

Received date: 2019-12-03

  Accepted date: 2020-05-09

  Online published: 2020-11-28

Abstract

Ustilaginoidea virens is the causal agent of rice false smut, which can be a highly destructive disease of rice. The plasma membrane phosphatase Psr1 proteins, which act as a regulator of the salinity stress response in yeast, are widely distributed across fungi, but their functional characterization is sketchy. In this study, we characterized the functions of Psr1 protein, UvPsr1, in U. virens. Analyses of the ∆Uvpsr1 and its complementation strain showed that UvPsr1 is required for normal mycelial growth, conidiation and tolerance to oxidative, osmotic and cell wall stresses. When rice panicles were inoculated with the ∆Uvpsr1 strains, no symptoms of false smut disease developed, showing that UvPSR1 also contributes to the pathogenicity of the fungus. The deletion mutant of UvPSR1 also appeared to produce a smaller titer of toxic compounds able to inhibit elongation of the germinated seeds. In conclusion, our results indicated that UvPsr1 is a new pathogenic factor of U. virens.

Cite this article

Meng Xiong, Shuai Meng, Jiehua Qiu, Huanbin Shi, Xiangling Shen, Yanjun Kou . Putative Phosphatase UvPsr1 Is Required for Mycelial Growth, Conidiation, Stress Response and Pathogenicity in Ustilaginonidea virens[J]. Rice Science, 2020 , 27(6) : 529 -536 . DOI: 10.1016/j.rsci.2020.09.009

References

[1] Ashizawa T, Takahashi M, Moriwaki J, Hirayae K.2010. A refined inoculation method to evaluate false smut resistance in rice. J Gen Plant Pathol, 77(1): 10-16.
[2] Boeckstaens M, Llinares E, van Vooren P, Marini A M.2014. The TORC1 effector kinase Npr1 fine tunes the inherent activity of the Mep2 ammonium transport protein. Nat Commun, 5: 3101.
[3] Chen X Y, Hai D, Tang J T, Liu H, Huang J B, Luo C X, Hsiang T, Zheng L.2020. UvCom1 is an important regulator required for development and infection in the rice false smut fungus Ustilaginoidea virens. Phytopathology, 110(2): 483-493.
[4] Chen Y Y, Stabryla L, Wei N.2016. Improved acetic acid resistance in Saccharomyces cerevisiae by overexpression of the WHI2 gene identified through inverse metabolic engineering. Appl Environ Microbiol, 82(7): 2156-2166.
[5] Fan J, Yang J, Wang Y Q, Li G B, Li Y, Huang F, Wang W M.2016. Current understanding on Villosiclava virens, a unique flower-infecting fungus causing rice false smut disease. Mol Plant Pathol, 17(9): 1321-1330.
[6] Fan J, Du N, Li L, Li G B, Wang Y Q, Zhou Y F, Hu X H, Liu J, Zhao J Q, Li Y, Huang F, Wang W M.2019. A core effector UV_1261 promotes Ustilaginoidea virens infection via spatiotemporally suppressing plant defense. Phytopathol Res, 1(1): 11.
[7] Fang A F, Gao H, Zhang N, Zheng X H, Qiu S S, Li Y J, Zhou S, Cui F H, Sun W X.2019. A novel effector gene SCRE2 contributes to full virulence of Ustilaginoidea virens to rice. Front Microbiol, 10: 845.
[8] Guo W W, Gao Y X, Yu Z M, Xiao Y H, Zhang Z G, Zhang H F.2019. The adenylate cyclase UvAc1 and phosphodiesterase UvPdeH control the intracellular cAMP level, development, and pathogenicity of the rice false smut fungus Ustilaginoidea virens. Fungal Genet Biol, 129: 65-73.
[9] Kaida D, Yashiroda H, Toh-e A, Kikuchi Y.2002. Yeast Whi2 and Psr1-phosphatase form a complex and regulate STRE-mediated gene expression. Genes Cells, 7(6): 543-552.
[10] Ladhalakshmi D, Laha G S, Singh R, Karthikeyan A, Mangrauthia S K, Sundaram R M, Thukkaiyannan P, Viraktamath B C.2012. Isolation and characterization of Ustilaginoidea virens and survey of false smut disease of rice in India. Phytoparasitica, 40(2): 171-176.
[11] Liang Y F, Han Y, Wang C F, Jiang C, Xu J R.2018. Targeted deletion of the USTA and UvSLT2 genes efficiently in Ustilaginoidea virens with the CRISPR-Cas9 system. Front Plant Sci, 9: 699.
[12] Lin X Y, Bian Y F, Mou R X, Cao Z Y, Cao Z Z, Zhu Z W, Chen M X.2018. Isolation, identification, and characterization of Ustilaginoidea virens from rice false smut balls with high ustilotoxin production potential. J Basic Microbiol, 58(8): 670-678.
[13] Lv B, Zheng L, Liu H, Tang J T, Hsiang T, Huang J B.2016. Use of random T-DNA mutagenesis in identification of gene UvPRO1, a regulator of conidiation, stress response, and virulence in Ustilaginoidea virens. Front Microbiol, 7: 2086.
[14] Nessa B, Salam M U, Haque A H M M, Biswas J K, Kabir M S, MacLeod W J, D’Antuono M, Barman H N, Latif M A, Galloway J.2015. Spatial pattern of natural spread of rice false smut Ustilaginoidea virens disease in fields. Am J Agric Biol Sci, 10(2): 63-73.
[15] Qiu J H, Meng S, Deng Y Z, Huang S W, Kou Y J.2019. Ustilaginoidea virens: A fungus infects rice flower and threats world rice production. Rice Sci, 26(4): 199-206.
[16] Tang J T, Bai J, Chen X Y, Zheng L, Liu H, Huang J B.2019. Two protein kinases UvPmk1 and UvCDC2 with significant functions in conidiation, stress response and pathogenicity of rice false smut fungus Ustilaginoidea virens. Curr Genet, 66: 409-420.
[17] Teng X C, Hardwick J M.2019. Whi2: A new player in amino acid sensing. Curr Genet, 65(3): 701-709.
[18] Timpano H, Tong L C H, Gautier V, Lalucque H, Silar P.2016. The PaPsr1 and PaWhi2 genes are members of the regulatory network that connect stationary phase to mycelium differentiation and reproduction in Podospora anserina. Fungal Genet Biol, 94: 1-10.
[19] Wang X H, Wang J, Lai D W, Wang W X, Dai J G, Zhou L G, Liu Y.2017. Ustiloxin G, a new cyclopeptide mycotoxin from rice false smut balls. Toxins, 9(2): E54.
[20] Xie S L, Wang Y F, Wei W, Li C Y, Liu Y, Qu J S, Meng Q H, Lin Y, Yin W X, Yang Y N, Luo C X.2019. The Bax inhibitor UvBI-1, a negative regulator of mycelial growth and conidiation, mediates stress response and is critical for pathogenicity of the rice false smut fungus Ustilaginoidea virens. Curr Genet, 65(5): 1185-1197.
[21] Yu M N, Yu J J, Hu J K, Huang L, Wang Y H, Yin X L, Nie Y F, Meng X K, Wang W D, Liu Y F.2015. Identification of pathogenicity-related genes in the rice pathogen Ustilaginoidea virens through random insertional mutagenesis. Fungal Genet Biol, 76: 10-19.
[22] Yun Y Z, Liu Z Y, Yin Y N, Jiang J H, Chen Y, Xu J R, Ma Z H.2015. Functional analysis of the Fusarium graminearum phosphatome. New Phytol, 207(1): 119-134.
[23] Zhang Y, Zhang K, Fang A F, Han Y Q, Yang J, Xue M F, Bao J D, Hu D W, Zhou B, Sun X Y, Li S J, Wen M, Yao N, Ma L J, Liu Y F, Zhang M, Huang F, Luo C X, Zhou L G, Li J Q, Chen Z Y, Miao J K, Wang S, Lai J S, Xu J R, Hsiang T, Peng Y L, Sun W X.2014. Specific adaptation of Ustilaginoidea virens in occupying host florets revealed by comparative and functional genomics. Nat Commun, 5: 3849.
[24] Zheng D W, Wang Y, Han Y, Xu J R, Wang C F.2016. UvHOG1 is important for hyphal growth and stress responses in the rice false smut fungus Ustilaginoidea virens. Sci Rep, 6: 24824.
[25] Zheng M T, Ding H, Huang L, Wang Y H, Yu M N, Zheng R, Yu J J, Liu Y F.2017. Low-affinity iron transport protein Uvt3277 is important for pathogenesis in the rice false smut fungus Ustilaginoidea virens. Curr Genet, 63(1): 131-144.
[26] Zhou Y X, Yu J J, Pan X Y, Yu M N, Du Y, Qi Z Q, Zhang R S, Song T Q, Yin X L, Liu Y F.2019. Characterization of propiconazole field-resistant isolates of Ustilaginoidea virens. Pestic Biochem Physiol, 153: 144-151.
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