Monitoring and analysis of rice pathogen Ustilaginoidea virens isolates with resistance to sterol demethylation inhibitors in China

被引:9
作者
Pan, Xiayan [1 ]
Cao, Huijuan [1 ]
Yu, Junjie [1 ]
Yu, Mina [1 ]
Qi, Zhongqiang [1 ]
Song, Tianqiao [1 ]
Du, Yan [1 ]
Yong, Mingli [1 ]
Zhang, Rongsheng [1 ]
Yin, Xiaole [1 ]
Liu, Yongfeng [1 ]
机构
[1] Jiangsu Acad Agr Sci, Inst Plant Protect, Nanjing 210014, Peoples R China
关键词
Ustilaginoidea virens; Propiconazole; Resistance monitoring; Fitness; AZOLE FUNGICIDE SENSITIVITY; GENETIC ELEMENT MONA; MYCOSPHAERELLA-GRAMINICOLA; TRANSCRIPTIONAL REGULATION; 14-ALPHA-DEMETHYLASE GENE; SACCHAROMYCES-CEREVISIAE; STRESS RESPONSES; CYP51; GENE; FALSE SMUT; OVEREXPRESSION;
D O I
10.1186/s42483-020-00062-x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Rice false smut (RFS), caused by Ustilaginoidea virens (Cooke) Takah, is an important fungal disease of rice. In China, sterol demethylation inhibitors (DMIs) are common fungicides used to control RFS. In a previous study, we detected two propiconazole-resistant U. virens isolates in 2015 in Huai'an city, Jiangsu Province, China. In the current study, we detected six propiconazole-resistant isolates out of 180U. virens isolates collected from rice fields in Jiangsu Province in 2017, and found they were from three different places (Xuzhou, Huai'an and Jintan). All these six propiconazole-resistant isolates were cross-resistant to three other sterol demethylation inhibitor (DMI) fungicides, i.e. difenoconazole, tebuconazole, and epoxiconazole. Among them, two isolates (2017-61 and 2017-170) had high fitness. Through sequencing and RT-qPCR analysis, we found that the expression levels of CYP51 and its encoded protein were significantly increased in the propiconazole-resistant isolates with a "CC" insertion mutation upstream of the CYP51 coding region compared to the propiconazole-sensitive isolates. In addition, propiconazole stimulated CYP51 expression in all isolates. Propiconazole also stimulated the accumulation of CYP51 protein in propiconazole-sensitive isolates and propiconazole-resistant isolates without mutation, but not in propiconazole-resistant isolates with the "CC" mutation. According to JASPAR database analysis, the predicated functional binding sites for propiconazole-resistant isolates with a "CC" insertion mutation and propiconazole-sensitive isolates were different. Given the high fitness of the propiconazole-resistant isolates, the development of resistance to DMIs in U. virens should be monitored. Furthermore, we speculated that the over-expression of CYP51 may contribute to DMI resistance in U. virens with the "CC" insertion mutation.
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页数:9
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