Target and nontarget mechanisms of AHAS inhibitor cross-resistance patterns in Cyperus difformis

被引:1
作者
Ceseski, Alex R. [1 ]
Godar, Amar S. [1 ]
Ohadi, Sara [1 ]
Al-Khatib, Kassim [1 ]
机构
[1] Univ Calif Davis, Dept Plant Sci, Mailstop 4,One Shields Ave, Davis, CA 95616 USA
关键词
Cyperus difformis; AHAS inhibitors; Cross-resistance; Nontarget resistance; SITE-BASED RESISTANCE; ACETOLACTATE SYNTHASE; ECHINOCHLOA-PHYLLOPOGON; HERBICIDE RESISTANCE; MOLECULAR-BASIS; RICE; MUTATION; ISSUES;
D O I
10.1016/j.pestbp.2023.105444
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Weed resistance to acetohydroxyacid synthase (AHAS) inhibiting herbicides has been a critical issue for rice growers worldwide since the early 1990's. In California, resistance to bensulfuron-methyl was first detected in Cyperus difformis in 1993. Since then, populations of most major weeds of rice in California have been reported to show resistance to at least one AHAS inhibitor. We sought to describe the magnitude and mechanisms of AHAS inhibitor cross-resistance in California populations of C. difformis. Sixty-two populations were collected and screened for cross-resistance to bensulfuron-methyl (BEN), halosulfuron-methyl (HAL), bispyribac-sodium (BIS), and penoxsulam (PEN), revealing six major patterns of cross-resistance. Representative C. difformis populations from each cross-resistance pattern were then subjected to dose-response, cytochrome P450 inhibition, AHAS gene sequencing, and metabolic studies with the same herbicides as in the screening. Dose-response confirmed the detected resistances in the representative populations, and suggested that the majority of observed resistance was dose-dependent. Cytochrome P450 inhibition via malathion revealed evidence of increased metabolic activity in resistant populations to BEN, BIS, and PEN. AHAS gene sequencing revealed amino acid substitutions in five of six populations: R3 (Pro197-Ser), R4 (Pro97-His), R10 (Asp376), R41 (Ala122-Asn), and R18 (Trp574Leu). Metabolic studies confirmed evidence of increased activity of cytochrome P450s in all populations. Metabolic BEN and HAL analysis did not yield similar results to malathion inhibition, suggesting different P450's or other pathways. Taken together, the results of the studies confirm the complexity of AHAS inhibitor crossresistance in C. difformis, and the presence of both target-site and metabolic resistance in most of the representative populations underscores the importance of proper herbicide selection, rotation, and scouting in fields.
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页数:11
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共 44 条
  • [1] Altop E.K., 2012, DETERMINATION ALS HE, P166
  • [2] Enhanced Herbicide Metabolism and Metabolic Resistance Genes Identified in Tribenuron-Methyl Resistant Myosoton aquaticum L.
    Bai, Shuang
    Liu, Weitang
    Wang, Hengzhi
    Zhao, Ning
    Jia, Sisi
    Zou, Nan
    Guo, Wenlei
    Wang, Jinxin
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2018, 66 (37) : 9850 - 9857
  • [3] Davis R.C., 1994, P C HELD LEET NEW S, P437
  • [4] The impact of uptake, translocation and metabolism on the differential selectivity between blackgrass and wheat for the herbicide pyroxsulam
    deBoer, Gerrit J.
    Thornburgh, Scott
    Gilbert, Jeff
    Gast, Roger E.
    [J]. PEST MANAGEMENT SCIENCE, 2011, 67 (03) : 279 - 286
  • [5] Unravelling the genetic bases of non-target-site-based resistance (NTSR) to herbicides: a major challenge for weed science in the forthcoming decade
    Delye, Christophe
    [J]. PEST MANAGEMENT SCIENCE, 2013, 69 (02) : 176 - 187
  • [6] CytochromeP450-mediated herbicide metabolism in plants: current understanding and prospects
    Dimaano, Nina Gracel
    Iwakami, Satoshi
    [J]. PEST MANAGEMENT SCIENCE, 2021, 77 (01) : 22 - 32
  • [7] Structure and mechanism of inhibition of plant acetohydroxyacid synthase
    Duggleby, Ronald G.
    McCourt, Jennifer A.
    Guddat, Luke W.
    [J]. PLANT PHYSIOLOGY AND BIOCHEMISTRY, 2008, 46 (03) : 309 - 324
  • [8] Fischer AJ, 2000, WEED SCI, V48, P225, DOI 10.1614/0043-1745(2000)048[0225:HREOAE]2.0.CO
  • [9] 2
  • [10] Garcia M.D., 2017, P NATL ACAD SCI