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甘蓝夜蛾对氯虫苯甲酰胺的抗性与 UDP-糖基转移酶基因 UGT2B17 的过度表达有关。

Over-expression of UDP-glycosyltransferase gene UGT2B17 is involved in chlorantraniliprole resistance in Plutella xylostella (L.).

机构信息

Department of Entomology, China Agricultural University, Beijing, P.R. China.

出版信息

Pest Manag Sci. 2017 Jul;73(7):1402-1409. doi: 10.1002/ps.4469. Epub 2016 Dec 19.

Abstract

BACKGROUND

UDP-glycosyltransferases (UGTs) are phase II detoxification enzymes widely distributed within living organisms. Their involvement in the biotransformation of various lipophilic endogenous compounds and phytoalexins in insects has been documented. However, the roles of this enzyme family in insecticide resistance have rarely been reported. Here, the functions of UGTs in chlorantraniliprole resistance in Plutella xylostella were investigated.

RESULTS

Treatment with sulfinpyrazone and 5-nitrouracil (both inhibitors of UGT enzymes) significantly increased the toxicity of chlorantraniliprole against the third instar larvae of P. xylostella. Among the 23 UGT transcripts examined, only UGT2B17 was found to be over-expressed (with a range from 30.7- to 77.3-fold) in all four chlorantraniliprole-resistant populations compared to the susceptible one (CHS). The knock-down of UGT2B17 by RNA interference (RNAi) dramatically increased the toxicity of chlorantraniliprole by 27.4% and 29.8% in the CHS and CHR (resistant) populations, respectively. In contrast, exposure to phenobarbital significantly increased the relative expression of UGT2B17 while decreasing the toxicity of chlorantraniliprole to the larvae by 14.0%.

CONCLUSION

UGT2B17 is involved in the detoxification of chlorantraniliprole, and its over-expression may play an important role in chlorantraniliprole resistance in P. xylostella. These results shed some light upon and further our understanding of the mechanisms of diamide insecticide resistance in insects. © 2016 Society of Chemical Industry.

摘要

背景

UDP-糖基转移酶(UGTs)是广泛分布于生物体内的Ⅱ相解毒酶。它们在昆虫体内各种亲脂性内源性化合物和植物抗毒素的生物转化中的作用已有文献记载。然而,该酶家族在杀虫剂抗性中的作用很少有报道。本研究探讨了 UGTs 在小菜蛾氯虫苯甲酰胺抗性中的作用。

结果

用磺吡酮和 5-硝基尿嘧啶(UGT 酶抑制剂)处理显著增加了氯虫苯甲酰胺对小菜蛾 3 龄幼虫的毒性。在所研究的 23 个 UGT 转录本中,只有 UGT2B17 在所有四个氯虫苯甲酰胺抗性种群中(与敏感种群 CHS 相比)过度表达(范围为 30.7-77.3 倍)。RNA 干扰(RNAi)敲低 UGT2B17 可使氯虫苯甲酰胺对 CHS 和 CHR(抗性)种群的毒性分别增加 27.4%和 29.8%。相比之下,暴露于苯巴比妥可显著增加 UGT2B17 的相对表达,同时使氯虫苯甲酰胺对幼虫的毒性降低 14.0%。

结论

UGT2B17 参与了氯虫苯甲酰胺的解毒,其过表达可能在小菜蛾对氯虫苯甲酰胺的抗性中起重要作用。这些结果为了解二酰胺类杀虫剂在昆虫中的抗性机制提供了一些启示。 © 2016 化学工业协会。

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