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Target site mutations and cytochrome P450s-involved metabolism confer resistance to nicosulfuron in green foxtail (Setaria viridis)

文献类型: 外文期刊

作者: Huang, Zhaofeng 1 ; Lu, Zongzhi 2 ; Huang, Hongjuan 1 ; Li, Wenyu 1 ; Cao, Yi 1 ; Wei, Shouhui 1 ;

作者机构: 1.Chinese Acad Agr Sci, Inst Plant Protect, Beijing 100193, Peoples R China

2.Jilin Acad Agr Sci, Inst Plant Protect, Changchun 130033, Jilin, Peoples R China

关键词: Nicosulfuron resistance; Acetolactate synthase (ALS); Setaria viridis; Metabolism; Cross resistance; Mutation

期刊名称:PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY ( 影响因子:3.963; 五年影响因子:4.454 )

ISSN: 0048-3575

年卷期: 2021 年 179 卷

页码:

收录情况: SCI

摘要: Green foxtail [Setaria viridis (L.) P.Beauv.] is a troublesome grass weed that is widely distributed in maize (Zea mays L.) fields across China. Many populations of S. viridis have evolved resistance to the acetolactate synthase (ALS)-inhibiting herbicide nicosulfuron. The objectives of this research were to confirm nicosulfuron resistance in these populations and to investigate the basis of nicosulfuron resistance. Whole-plant dose-response experiments showed 6 out of 13 S. viridis populations were highly resistance (20-30 times) to nicosulfuron. Sequencing of the ALS gene revealed two amino acid mutations, Asp-376-Glu and Pro-197-Ala, in the nicosulfuron-resistant populations. A malathion pretreatment study revealed that the R376 and R197 subpopulations might have cytochrome P450s-mediated herbicide metabolic resistance. The resistant populations were cross-resistant to imazethapyr but sensitive to topramezone and quizalofop-p-ethyl. This is the first report of resistance to ALS inhibitors conferred by target site mutations (Asp-376-Glu or Pro-197-Ser) and possible cytochrome P450sinvolved metabolism in S. viridis.

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