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中国萤蔺对噁唑磺草酮的靶标和代谢抗性机制。

Target-Site and Metabolic Resistance Mechanisms to Penoxsulam in Late Watergrass () in China.

机构信息

College of Plant Protection, Nanjing Agricultural University, Nanjing 210095, China.

State & Local Joint Engineering Research Center of Green Pesticide Invention and Application, Nanjing 210095, China.

出版信息

J Agric Food Chem. 2023 Nov 22;71(46):17742-17751. doi: 10.1021/acs.jafc.3c05921. Epub 2023 Nov 7.

Abstract

, a malignant weed in Northeast China's paddy fields, is currently presenting escalating resistance concerns. Our study centered on the HJHL-715 population, which showed heightened resistance to penoxsulam, through a whole-plant bioassay. Pretreatment with a P450 inhibitor malathion significantly increased penoxsulam sensitivity in resistant plants. In order to determine the resistance mechanism of the resistant population, we purified the resistant population from individual plants and isolated target-site resistance (TSR) and nontarget-site resistance (NTSR) materials. Pro-197-Thr and Trp-574-Leu mutations in acetolactate synthase (ALS) 1 and ALS2 of the resistant population drove reduced sensitivity of penoxsulam to the target-site ALS, the primary resistance mechanisms. To fully understand the NTSR mechanism, NTSR materials were investigated by using RNA-sequencing (RNA-seq) combined with a reference genome. High-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) analysis further supported the enhanced penoxsulam metabolism in NTSR materials. Gene expression data and quantitative reverse transcription polymerase chain reaction (qRT-PCR) validation confirmed 29 overexpressed genes under penoxsulam treatment, with 16 genes concurrently upregulated with quinclorac and metamifop treatment. Overall, our study confirmed coexisting TSR and NTSR mechanisms in 's resistance to ALS inhibitors.

摘要

稗草是中国东北地区稻田中的一种恶性杂草,目前其抗药性问题日益严重。本研究以对吡嘧磺隆表现出较高抗药性的 HJHL-715 种群为研究对象,通过整株生物测定法进行研究。用 P450 抑制剂马拉硫磷预处理可显著提高抗性植株中吡嘧磺隆的敏感性。为了确定抗性种群的抗性机制,我们从单株植物中分离出抗性种群,并分离出靶标位点抗性(TSR)和非靶标位点抗性(NTSR)材料。抗性种群中乙酰乳酸合成酶(ALS)1 和 ALS2 的 Pro-197-Thr 和 Trp-574-Leu 突变导致靶标 ALS 对吡嘧磺隆的敏感性降低,这是主要的抗性机制。为了全面了解 NTSR 机制,我们使用 RNA 测序(RNA-seq)结合参考基因组研究了 NTSR 材料。高效液相色谱-串联质谱(HPLC-MS/MS)分析进一步支持了 NTSR 材料中吡嘧磺隆代谢的增强。基因表达数据和定量反转录聚合酶链反应(qRT-PCR)验证证实了 29 个在吡嘧磺隆处理下过表达的基因,其中 16 个基因与吡嘧磺隆和唑草酮处理同时上调。总之,本研究证实了稗草对 ALS 抑制剂的抗性存在 TSR 和 NTSR 共存机制。

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