A key amino acid substitution of vacuolar-type H+-ATPases A subunit (VATP-A) confers selective toxicity of a potential botanical insecticide, periplocoside P (PSP), in Mythimna separata and Spodoptera exigua.

Abstract

Periplocosides, extracted from the root bark of Periploca sepium, are plant secondary compounds known to inhibit the V-ATPase enzyme in susceptible insect species, such as Mythimna separata. However, many species, including Spodoptera exigua, show resistance to these compounds. Previous studies identified the V-ATPase subunit A (VATP-A) in the midgut epithelium of M. separata as the putative target of periplocoside P (PSP), but the specific amino acids involved in this interaction remained unclear. In this study, we demonstrate the selective toxicity of PSP and its inhibition effect on V-ATPase. Molecular docking identified potential interactions between PSP and three amino acids (K85, R171, E199) in MsVATP-A, with in vitro binding assays revealing that K85 and R171 serve as the primary binding sites. Notably, sequence alignment revealed that R171 in sensitive species is substituted with K in resistant species. To investigate the functional implications of this substitution, we performed in vitro site-directed mutagenesis to exchange the corresponding amino acids between the VATP-A orthologs of M. separata and S. exigua. The R171K mutation in MsVATP-A reduced binding to PSP, while the K170R mutation in SeVATP-A enhanced it. Furthermore, in vivo genome editing in Drosophila melanogaster, a PSP-sensitive species, revealed that the R171K mutation conferred 15.78-fold resistance to PSP compared to the wild-type strain (w¹¹¹⁸). Our findings confirm the role of VATP-A as the target of PSP and elucidate the key amino acids influencing its insecticidal selectivity. This research enhances the understanding of the molecular interactions between natural compounds and insect targets, offering insights for the development of targeted pest control strategies.