Multiomics Approaches to Study the Contact Toxicity and Mechanisms of Aliphatic Ketones and Aldehydes against Tribolium castaneum.

Tribolium castaneum is a major pest of stored grain products. This research aimed to investigate how structural variation in plant-derived aliphatic ketones and aldehydes influenced contact toxicity against T. castaneum. 2-Dodecanone (Do, C12) demonstrated the greatest contact toxicity (LD50 = 14.9 μg/larva), substantially exceeding its isomer dodecanal (Da, LD50 = 30.0 μg/larva). Toxicity peaked at 12 carbons and declined as chain length increased or decreased, with 2-heptanone (Ho, C7) being the least active (LD50 = 43.5 μg/larva). Integrated transcriptomic, proteomic, metabolomic, and RNA-interference analyses revealed compound-specific mechanisms. Do penetrated the cuticle efficiently owing to its higher lipophilicity, activating phase I detoxification (CYP6BQ7, CYP345A1, CYP345D2) and hormone biosynthesis (FDa). Da induced phase 0 handling through OBP-C11 and downregulated cuticle protein via LCPF-like. Ho triggered structural defenses, with SSP2-like upregulation and CSP10 downregulation. Metabolomics showed Da predominantly produced organic acids and derivatives, while Do and Ho yielded lipids and lipid-like metabolites, reflecting divergent biotransformation routes. These findings clarify structure-activity relationships and identify molecular targets for designing safe, effective grain protectants.