Aminotransferase SsAro8 Regulates Tryptophan Metabolism Essential for Filamentous Growth of Sugarcane Smut Fungus Sporisorium scitamineum

被引:10
|
作者
Cui, Guobing [1 ,2 ]
Huang, Chengwei [1 ,4 ]
Bi, Xinping [1 ,2 ]
Wang, Yixu [1 ,5 ]
Yin, Kai [1 ,2 ]
Zhu, Luyuan [1 ,2 ]
Jiang, Zide [1 ]
Chen, Baoshan [3 ]
Deng, Yi Zhen [1 ,2 ]
机构
[1] South China Agr Univ, State Key Lab Conservat & Utilizat Subtrop Agrobi, Guangdong Prov Key Lab Microbial Signals & Dis Co, Integrat Microbiol Res Ctr, Guangzhou, Peoples R China
[2] Guangdong Lab Lingnan Modern Agr, Guangzhou, Peoples R China
[3] Guangxi Univ, Coll Life Sci & Technol, State Key Lab Conservat & Utilizat Subtrop Agrobi, Nanning, Peoples R China
[4] Wuhan Univ, Coll Life Sci, Wuhan, Hubei, Peoples R China
[5] Int Ctr Genet Engn & Biotechnol, Trieste, Italy
来源
MICROBIOLOGY SPECTRUM | 2022年 / 10卷 / 04期
基金
中国国家自然科学基金;
关键词
Aro8; Sporisorium scitamineum; aromatic alcohols; filamentous growth; fungus; pathogenicity; sugarcane smut; tryptophol; AUXIN BIOSYNTHESIS; SACCHAROMYCES-CEREVISIAE; CANDIDA-ALBICANS; QUORUM; ACID; GENE; SACCHAROMYCES-CEREVISIAE-ARO8; INFLORESCENCE; MOLECULE; PATHWAY;
D O I
10.1128/spectrum.00570-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sugarcane smut caused by the basidiomycetous fungus Sporisorium scitamineum leads to severe economic losses globally. Sexual mating/filamentation of S. scitamineum is critical for its pathogenicity, as only the dikaryotic hyphae formed after sexual mating are capable of invading the host cane. Our comparative transcriptome analysis showed that the mitogen-activated protein kinase (MAPK) pathway and the AGC kinase Agc1 (orthologous to yeast Rim15), both governing S. scitamineum mating/filamentation, were induced by elevated tryptophol level, supporting a positive regulation of S. scitamineum mating/filamentation by tryptophol. However, the biosynthesis pathway of tryptophol remains unknown in S. scitamineum. Here, we identified an aminotransferase orthologous to the established tryptophan aminotransferase Tam1/Aro8, catalyzing the first step of tryptophan-dependent indole-3-acetic acid (IAA) production as well as that of the Ehrlich pathway for tryptophol production. We designated this S. scitamineum aminotransferase as SsAro8 and found that it was essential for mating/filamentation. Comparative metabolomics analysis revealed that SsAro8 was involved in tryptophan metabolism, likely for producing important intermediate products, including tryptophol. Exogenous addition of tryptophan or tryptophol could differentially restore mating/filamentation in the ssaro8 Delta mutant, indicating that in addition to tryptophol, other product(s) of tryptophan catabolism may also be involved in S. scitamineum mating/filamentation regulation. S. scitamineum could also produce IAA, partially dependent on SsAro8 function. Surprisingly, photodestruction of IAA produced the compound(s) able to suppress S. scitamineum growth/differentiation. Lastly, we found that SsAro8 was required for proper biofilm formation, oxidative stress tolerance, and full pathogenicity in S. scitamineum. Overall, our study establishes the aminotransferase SsAro8 as an essential regulator of S. scitamineum pathogenic differentiation, as well as fungus-host interaction, and therefore of great potential as a molecular target for sugarcane smut disease control. IMPORTANCE Sugarcane smut caused by the basidiomycete fungus S. scitamineum leads to massive economic losses in sugarcane plantation globally. Dikaryotic hyphae formation (filamentous growth) and biofilm formation are two important aspects in S. scitamineum pathogenesis, yet the molecular regulation of these two processes was not as extensively investigated as that in the model pathogenic fungi, e.g., Candida albicans, Ustilago maydis, or Cryptococcus neoformans. In this study, a tryptophan aminotransferase ortholog was identified in S. scitamineum, designated SsAro8. Functional characterization showed that SsAro8 positively regulates both filamentous growth and biofilm formation, respectively, via tryptophol-dependent and -independent manners. Furthermore, SsAro8 is required for full pathogenicity and, thus, is a promising molecular target for designing anti-smut strategy.
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页数:18
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