Suppr超能文献

氰氟虫腙抗性在朱砂叶螨中的稳定性及其与谷胱甘肽-S-转移酶基因表达的相关性。

Stability of cyflumetofen resistance in Tetranychus cinnabarinus and its correlation with glutathione-S-transferase gene expression.

机构信息

Department of pesticide, Key Laboratory of Entomology and Pest Control Engineering, College of Plant Protection, Southwest University, Chongqing, China.

Department of pesticide, Academy of Agricultural Sciences, Southwest University, Chongqing, China.

出版信息

Pest Manag Sci. 2019 Oct;75(10):2802-2809. doi: 10.1002/ps.5392. Epub 2019 Mar 25.

Abstract

BACKGROUND

Cyflumetofen is an outstanding acaricide with a novel mode of action. Tetranychus cinnabarinus, an important agricultural pest, is notorious for developing resistance to most classes of acaricides rapidly and results in enormous loss for the economy. Our previous study had pointed out glutathione S-transferase (GSTs) significantly contributed to the cyflumetofen-resistance formation in T. cinnabarinus, but the more specific mechanism needed to be further investigated.

RESULTS

The unstable resistance was observed in cyflumetofen-resistant strain (CyR)under acaricide-free condition. The activity of GSTs increased along with the development of resistance. The expressions of 13 GST genes were detected in CyR and susceptible strain (SS), of which six genes were overexpressed in CyR and the TcGSTm02 was selected as the representative for functional study. The expression of TcGSTm02 changed along with the resistant level of CyR with the same trend. Recombinant protein of TcGSTm02 with high activity was successfully obtained by E. coli expression system, whose activity could be inhibited by cyflumetofen (IC = 0.23 mM). Recombinant TcGSTm02 could effectively decompose cyflumetofen, and catalyze GS to conjugate with cyflumetofen.

CONCLUSION

All clues confirmed that GSTs strongly associated with cyflumetofen-resistance and a representative gene, TcGSTm02, showed function on contributing the evolution of cyflumetofen-resistance in T. cinnabarinus. © 2019 Society of Chemical Industry.

摘要

背景

氟吡呋喃酮是一种作用机制新颖的优秀杀螨剂。朱砂叶螨是一种重要的农业害虫,由于其对大多数类杀螨剂迅速产生抗性,导致经济损失巨大,因此声名狼藉。我们之前的研究指出,谷胱甘肽 S-转移酶(GSTs)对朱砂叶螨对氟吡呋喃酮的抗性形成有重要贡献,但需要进一步研究更具体的机制。

结果

在无杀螨剂条件下,观察到氟吡呋喃酮抗性品系(CyR)出现不稳定抗性。GSTs 的活性随着抗性的发展而增加。在 CyR 和敏感品系(SS)中检测到 13 个 GST 基因的表达,其中 6 个基因在 CyR 中过表达,选择 TcGSTm02 作为功能研究的代表。TcGSTm02 的表达随 CyR 抗性水平的变化而变化,趋势相同。通过大肠杆菌表达系统成功获得了具有高活性的 TcGSTm02 重组蛋白,其活性可被氟吡呋喃酮抑制(IC = 0.23 mM)。重组 TcGSTm02 可有效分解氟吡呋喃酮,并催化 GS 与氟吡呋喃酮结合。

结论

所有线索都证实 GSTs 与氟吡呋喃酮抗性密切相关,代表性基因 TcGSTm02 对朱砂叶螨对氟吡呋喃酮抗性的进化具有功能。© 2019 化学工业协会。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验