Abstract

Sugarcane is an important sugar crop. Sugarcane smut, caused by Sporisorium scitamineum, is a worldwide sugarcane disease with serious economic losses and lack of effective control measures. Revealing the molecular pathogenesis of S. scitamineum is very helpful to the development of effective prevention and control technology. Deubiquitinase removes ubiquitin molecules from their binding substrates and participates in a variety of physiological activities in eukaryotes. Based on the transcriptome sequencing data of two isolates (Ss16 and Ss47) of S. scitamineum with different pathogenicities, SsCI33130, a gene encoding an OTU1-deubiquitin enzyme, was identified. The positive knockout mutants and complementary mutants of the SsCI33130 gene were successfully obtained through polyethylene glycol-mediated protoplast transformation technology. In order to study the possible function of this gene in pathogenicity, phenotypic comparison of the growth, morphology, abiotic stress, sexual mating, pathogenicity, and gene expression levels of the knockout mutants, complementary mutants, and their wild type strains were conducted. The results demonstrated that the gene had almost no effect on abiotic stress, cell wall integrity, growth, and morphology, but was related to the sexual mating and pathogenicity of S. scitamineum. The sexual mating ability and pathogenicity between the knockout mutants or between the knockout mutant and wild type were more significantly reduced than between the wild types, the complementary mutants, or the wild types and complementary mutants. The sexual mating between the knockout mutants or between the knockout mutant and wild type could be restored by the exogenous addition of small-molecule signaling substances such as 5 mM cyclic adenosine monophosphate (cAMP) or 0.02 mM tryptophol. In addition, during sexual mating, the expression levels of tryptophol and cAMP synthesis-related genes in the knockout mutant combinations were significantly lower than those in the wild type combinations, while the expression levels in the complementary mutant combinations were restored to the level of the wild type. It is speculated that the SsCI33130 gene may be involved in the development of sexual mating and pathogenicity in S. scitamineum by regulating the synthesis of the small-molecule signaling substances (cAMP or tryptophol) required during the sexual mating of S. scitamineum, thereby providing a molecular basis for the study of the pathogenic mechanisms of S. scitamineum.

Highlights

  • Sugarcane is an important sugar crop and a potential renewable biomass energy crop

  • It was found that the activity of OTU1-deubiquitinase in the knockout mutants was always significantly lower than that in the wild types, and the activity of OTU1-deubiquitinase in the complementary mutants returned to the wild type level, which verified the accuracy of the gene encoding OTU1-deubiquitinase

  • The SsCI33130 gene knockout mutant exhibited no expression during haploid spore culture, sexual mating, or sugarcane bud infection, but the gene expression level of the complementary mutant was restored to the wild type level in the above process, which indicated that the knockout mutant and complementary mutant obtained in this study were effective, providing a foundation for further analysis

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Summary

Introduction

Sugarcane is an important sugar crop and a potential renewable biomass energy crop. Sugarcane smut is a significant disease affecting sugarcane worldwide. The main sugarcane cultivars in China are commonly infected with sugarcane smut, with a field incidence of 15–25%, and up to 50% of fields experience severe disease or even the loss of harvest (Shen et al, 2016b; Deng et al, 2020). Sugarcane smut is caused by Sporisorium scitamineum, which can be divided into a haploid spore stage and dikaryotic mycelium stage (Que et al, 2014). The two opposite mating types of haploid spores can form white or yellow villous dikaryotic mycelia by sexual mating, which can infect the host sugarcane (Alexander and Srinivasan, 1966; Albert and Schenck, 1996; Yan et al, 2016a; Zhang et al, 2019)

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