The caterpillars of the Lepidoptera are important herbivores as most of them belong to serious agricultural and forestry pests. To adapt to their habitats and feeding host plants, the larvae utilize uridine diphosphate (UDP)-glycosyltransferases (UGTs) to metabolize plant defensive compounds and insecticides. However, information on the UGT gene family in Achelura yunnanensis remains scarce. Here, we characterized the UGT genes through gene identification, phylogenic analyses, and comprehensive expression profiles regarding sexes, tissues, and stages. Transcriptome analyses led to the yields of 50 transcripts encoding UGTs in A. yunnanensis, representing a comparable gene number compared to those in other lepidopteran species. Sequence and phylogenetic analyses revealed a low amino acid identity of 28.23% among 31 full-length AyunUGTs, but some members shared relatively high conservation (>50% identities) with a phylogenetically clustered distribution. In addition, the majority of AyunUGTs possessed conserved residues involved in the catalysis and sugar-donor binding. Combining RNA sequencing and PCR approaches, a number of AyunUGTs were found to have the expression in chemosensory or detoxification tissues, possibly associated with the sensing of odorant molecules and the metabolism of toxic chemicals. More importantly, at least 27 AyunUGTs displayed detectable expression in reproductive tissues of both sexes. This study identifies candidate A. yunnanensis UGTs responsible for detoxification, olfaction, and reproduction, allowing us to address putative roles of UGTs in the adaptation of larvae to the habitats and feeding hosts.

The wood-boring beetles, including the majority of Cerambycidae, have developed the ability to metabolize a variety of toxic compounds derived from host plants and the surrounding environment. However, detoxification mechanisms underlying the evolutionary adaptation of a cerambycid beetle Pharsalia antennata to hosts and habitats are largely unexplored. Here, we characterized three key gene families in relation to detoxification (cytochrome P450 monooxygenases: P450s, carboxylesterases: COEs and glutathione-Stransferases: GSTs), by combinations of transcriptomics, gene identification, phylogenetics and expression profiles. Illumina sequencing generated 668,701,566 filtered reads in 12 tissues of P. antennata, summing to 100.28 gigabases data. From the transcriptome, 215 genes encoding 106 P450s, 77 COEs and 32 GSTs were identified, of which 107 relatives were differentially expressed genes. Of the identified 215 genes, a number of relatives showed the orthology to those in Anoplophora glabripennis, revealing 1:1 relationships in 94 phylogenetic clades. In the trees, P. antennata detoxification genes mainly clustered into one or two subfamilies, including 64 P450s in the CYP3 clan, 33 COEs in clade A, and 20 GSTs in Delta and Epsilon subclasses. Combining transcriptomic data and PCR approaches, the numbers of detoxification genes expressed in abdomens, antennae and legs were 188, 148 and 141, respectively. Notably, some genes exhibited significantly sexbiased levels in antennae or legs of both sexes. The findings provide valuable reference resources for further exploring xenobiotics metabolism and odorant detection in P. antennata.