The soybean pod borer, Leguminivora glycinivorella, is a monophagous pest that threatens soybean production. Its larvae feed concealed within pods, which limits the efficacy of conventional insecticides. Elucidating its chemosensory system is therefore essential for developing green, behavior-based management strategies. Reference-based transcriptomics across multiple tissues of L. glycinivorella identified a comprehensive repertoire of chemosensory genes, including 76 odorant receptors (ORs), 15 gustatory receptors (GRs), 18 ionotropic receptors (IRs), 52 odorant-binding proteins (OBPs), 18 chemosensory proteins (CSPs), and 4 sensory neuron membrane proteins (SNMPs). Sequence and phylogenetic analyses characterized these candidates within the context of known insect chemosensory families. Notably, canonical bitter GRs and specific IR lineages (e.g., IR100/IR85a) were not detected in our dataset, potentially reflecting adaptation to the specialized soybean-feeding habit of this pest. Expression profiling further revealed pronounced sexual and tissue dimorphism: male antennae showed significant enrichment of putative pheromone receptors (PRs) and LglySNMP1, whereas several OBPs and ORs exhibited female-biased expression, suggesting roles in host location and oviposition. Additionally, the high expression of GR43a homologs points to fructose sensing, while the lack of detectable CO₂ receptor components (except LglyGR2) suggests atypical carbon dioxide perception mechanisms. Collectively, this study provides a valuable expression atlas of chemosensory genes in L. glycinivorella and identifies sex-specific candidate genes for future functional validation and behavior-based pest management.

Thiamethoxam is the main neonicotinoid insecticide used for controlling Riptortus pedestris (Fabricius) (Hemiptera: Alydidae). However, sublethal concentration stress may induce intergenerational transcriptional memory, leading to transcriptional patterns that may contribute to the intergenerational accumulation of metabolic tolerance, and evaluating only the toxicity of the current generation would underestimate the long-term risk. Therefore, this study investigated the effect of parental exposure on the expression of detoxification enzyme genes in offspring. Using transcriptome sequencing, we systematically identified three detoxification enzyme gene families (cytochrome P450 monooxygenases (CYPs), carboxylesterases (CCEs), and glutathione S-transferases (GSTs)) in R. pedestris and compared their differential expression patterns between the parental and filial generations after thiamethoxam treatment at three sublethal concentrations (LC₁₀, LC₃₀, and LC₅₀). In the parental generation, a Theta family GST was consistently upregulated, while in the filial generation, detoxification genes were predominantly downregulated, and the genes upregulated in the parents were not also upregulated in the offspring. Comparisons of parents and offspring at the same concentration revealed that the medium concentration induced the highest number of intergenerationally upregulated genes, exhibiting a non-linear response pattern. These results indicate that parental exposure to sublethal thiamethoxam leaves an intergenerational transcriptional imprint in the offspring, and the transmission pattern involves transcriptional reprogramming rather than simple replication of the parental response, the mechanism of which remains to be determined. This study provides transcriptomic evidence for understanding the metabolic adaptation and intergenerational resistance evolution of R. pedestris to thiamethoxam, offering important reference value for field resistance monitoring and rational insecticide application.