In insects, the olfactory system governs physiological and behavioral processes by detecting various odorous molecules. Despite its economic importance and adaptability, the olfactory mechanism of Antheraea pernyi remains insufficiently understood, limiting its potential for pest management and as a model organism. Hence, we aimed to conduct transcriptome sequencing to explore olfactory-related genes in the antennae, serving as the most important olfactory organ in adult A. pernyi. Based on the datasets, 1184 differently expressed genes (DEGs), including 484 upregulated and 700 downregulated genes, were identified by comparing the transcriptome profiles of the male and female antennae of A. pernyi. Moreover, 20, 7, 30, 11, and 2 candidate genes encoding odorant‐binding proteins (OBPs), chemosensory proteins (CSPs), odorant receptors (ORs), ionotropic receptors (IRs), and sensory neuron membrane proteins (SNMPs), respectively, involved in pheromone perception, odor binding, pesticide resistance, and growth and development regulation were screened, and most of which were expressed in both male and female antennae while the expression levels of these candidate genes varied significantly between males and females. Multiple sequence alignment indicated that the six OBPs exhibited typical characteristics, containing six conserved Cys residues with the sequence of C1-X26-30-C2-X3-C3-X41-42-C4-X8-10-C5-X8-C6. All CSPs followed a highly conserved pattern with four Cys residues arranged with an exact spacing of C1-X6-C2-X18-19-C3-X2-C4. Different numbers of transmembrane domains were found in ORs, IRs, and SNMPs. In addition, several DEGs involve signal transduction underlying chemoreception were also identified from the transcriptome data, including guanine nucleotide-binding protein (G protein), cGMP-dependent protein kinase (PKA), calmodulin-A (CaM-A), mitogen-activated protein kinase 1 (MAPK1), and phospholipase D2 (PLD2). This study enriches the olfactory gene database of A. pernyi, providing insights into olfactory mechanisms crucial for mating and pest control, with implications for enhancing breeding strategies and ensuring the sustainability of the silk industry. These findings may serve as a theoretical foundation for a better understanding of the olfactory mechanisms of A. pernyi.

The proteome profiles of the cuticle and haemolymph of two strains of the Chinese Oak silk moth A. pernyi, with cyan and yellow coloured bodies, were compared in order to identify the differentially expressed proteins (DEPs) that determine the differences in the colouration of the two strains. A total of 324 DEPs, including 124 up-regulated and 200 down-regulated proteins, were identified in the cuticles of the cyan and yellow coloured individuals, and 286 DEPs including 79 up-regulated and 207 down-regulated proteins in the haemolymph of the cyan and yellow coloured individuals. Several DEPs associated with the colour of larvae of A. pernyi were screened, including an ommochrome-binding protein, juvenile hormone esterase, protein yellow, L-dopachrome tautomerase yellow-f2 and fumarylacetoacetase, the expression levels in the cuticle and haemolymph of the yellow larvae were higher than those in the cyan coloured larvae, indicating their possible roles underlying the colouration of the yellow larvae of A. pernyi.