4.7 Article

The role of Glutathione-S-transferases in phoxim and chlorfenapyr tolerance in a major mulberry pest, Glyphodes pyloalis walker (Lepidoptera: Pyralidae)

Journal

PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY
Volume 181, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pestbp.2021.105004

Keywords

Glyphodes pyloalis; Glutathione-S-transferases; Insecticides; RNAi; Tolerance

Funding

  1. Qing Lan Project of Jiangsu Province
  2. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX21_3438]
  3. Jiangsu Agricultural Science and Technology Innovation Fund [CX(21)3179]
  4. Key Project of University Science Research of Jiangsu Province [20KJA210004]
  5. Key Research and Development Program (Modern Agriculture) of Zhenjiang City [NY2019021]
  6. National Natural Science Foundation of China [31500312]

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Glyphodes pyloalis, a destructive pest on mulberry trees, poses a significant threat to the sericultural industry in China. This study reveals the important roles of glutathione-S-transferases (GSTs) in the tolerance of the insecticides phoxim and chlorfenapyr in G. pyloalis.
Glyphodes pyloalis Walker is a destructive pest on mulberry trees and poses a significant threat to the sericultural industry in China. Phoxim and chlorfenapyr are two commonly used insecticides in mulberry fields. Glutathione-S-transferases (GSTs) comprise a multifunctional protein superfamily that plays important roles in the detoxification of insecticides and xenobiotic compounds in insects. However, whether GSTs participate in the tolerance of phoxim and chlorfenapyr in G. pyloalis is still unknown. To better understand the mechanism of insecticide tolerance in G. pyloalis, the enzymatic activity of GSTs was evaluated under phoxim and chlorfenapyr exposure, respectively. GST enzyme activity was significantly increased after 12, 36 and 48 h of phoxim treatment and 12, 24, 36 and 48 h of chlorfenapyr treatment. Subsequently, eighteen GST genes were identified from the larvae transcriptome of G. pyloalis. Among these, ten GpGSTs had GSH-binding sites and fifteen GpGSTs had variable hydrophobic substrate-binding sites. The expression levels of Delta-GpGST and Epsilon-GpGST genes were significantly influenced by phoxim and chlorfenapyr treatment, and by the time post insecticide application. Furthermore, after silencing GpGST-E4, the mortality rate of G. pyloalis larvae was increased when they were exposed to chlorfenapyr, but it did not significantly alter when the larvae were exposed to phoxim. Our results indicated the vital roles of GpGSTs in the tolerance of insecticides and this action depends on the categories of insecticides. The present study provides a theoretical basis for elucidating insecticide susceptibility and promotes functional research on GST genes in G. pyloalis.

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