Identification of differentially expressed miRNAs associated with diamide detoxification pathways in Spodoptera frugiperda

Abstract

The fall armyworm (FAW) Spodoptera frugiperda is a severe economic pest of multiple crops globally. Control of this pest is often achieved using insecticides; however, over time, S. frugiperda has developed resistance to new mode of action compounds, including diamides. Previous studies have indicated diamide resistance is a complex developmental process involving multiple detoxification genes. Still, the mechanism underlying the possible involvement of microRNAs in post-transcriptional regulation of resistance has not yet been elucidated. In this study, a global screen of microRNAs (miRNAs) revealed 109 known and 63 novel miRNAs. Nine miRNAs (four known and five novel) were differentially expressed between insecticide-resistant and -susceptible strains. Gene Ontology analysis predicted putative target transcripts of the differentially expressed miRNAs encoding significant genes belonging to detoxification pathways. Additionally, miRNAs are involved in response to diamide exposure, indicating they are probably associated with the detoxification pathway. Thus, this study provides comprehensive evidence for the link between repressed miRNA expression and induced target transcripts that possibly mediate diamide resistance through post-transcriptional regulation. These findings highlight important clues for further research to unravel the roles and mechanisms of miRNAs in conferring diamide resistance.

The genetic architecture of resistance to flubendiamide insecticides inHelicoverpa armigera(Hübner) (Lepidoptera: Noctuidae)

“…Many studies have reported the involvement of ABC transporters in chlorantraniliprole and flubendiamide detoxification in other species such as Chilo suppressalis (Walker) (Lepidoptera: Crambidae) [53], P. xylostella [54], S. frugiperda [55] and Leptinotarsa decemlineata (Say) (Coleoptera: Chrysomelidae) [44]. The Multidrug resistance-associated protein 1 (MDR1), also known as P-glycoprotein (P-gp), is encoded by ATP-binding cassette subfamily B member 1 (ABCB1) [56,57].…”