4.7 Article

Role of the epsilon glutathione S-transferases in xanthotoxin tolerance in Spodoptera litura

Journal

PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY
Volume 196, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pestbp.2023.105592

Keywords

Xanthotoxin; Phytochemical tolerance; Molecular docking; Transcriptional regulation

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This study characterized twenty epsilon glutathione S-transferase genes (GSTes) in Spodoptera litura and analyzed their roles in phytochemical tolerance. Xanthotoxin, a phytochemical, induced the expression of most GSTe genes and formed stable bonds with six specific GSTes. Knockdown of these specific GSTe genes increased the larval susceptibility to xanthotoxin. Transcription factors CncC and MafK enhanced the expression of GSTe16, leading to increased xanthotoxin tolerance. The findings provide insight into the functions and transcriptional regulatory mechanisms of GSTes in the adaptation of S. litura to phytochemicals.
Spodoptera litura, a polyphagous lepidopteran pest, demonstrates a remarkable capacity to adapt to varying host plants by efficiently detoxifying phytochemicals. However, the underlying mechanism for this adaptation is not well understood. Herein, twenty eplison glutathione S-transferase genes (GSTes) were characterized and their roles in phytochemical tolerance were analyzed in S. litura. Most of the GSTe genes were mainly expressed in the larval midgut and fat body. Exposure to the phytochemicals, especially xanthotoxin, induced the expression of most GSTe genes. Molecular docking analysis revealed that xanthotoxin could form stable bonds with six xanthotoxin-responsive GSTes, with binding free energies ranging from -36.44 to -68.83 kcal mol-1. Knockdown of these six GSTe genes increased the larval susceptibility to xanthotoxin. Furthermore, xanthotoxin exposure significantly upregulated the expression of two transcription factor genes CncC and MafK. Silencing of either CncC or MafK reduced the expression of GSTe16, which exhibited the largest change in response to xanthotoxin. Additionally, analysis of the promoter sequence of GSTe16 revealed the presence of seven CncC/ Maf binding sites. Luciferase reporter assays showed that CncC and MafK enhanced the expression of GSTe16, leading to the increased xanthotoxin tolerance in S. litura. These findings provide insight into the functions and transcriptional regulatory mechanisms of GSTes, thereby enhancing our understanding of the role of GSTs in the adaptation of lepidopteran pests to phytochemicals.

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