Li Zhao-Qun, Cai Xiao-Ming, Luo Zong-Xiu, Bian Lei, Xin Zhao-Jun, Chu Bo, Liu Yan, Chen Zong-Mao
Key Laboratory of Tea Biology and Resource Utilization, Ministry of Agriculture, Tea Research Institute, Chinese Academy of Agricultural Sciences, Hangzhou, China.
Front Physiol. 2018 Nov 14;9:1602. doi: 10.3389/fphys.2018.01602. eCollection 2018.
The sibling species and are the major chewing tea pests in China. A difference in sex pheromone components plays a central role in premating isolation in these two species. To investigate the mechanism of premating isolation in these two species, we sequenced the transcriptomes of the antennae of female and male individuals and performed phylogenetic analyses, abundance analyses, and tissue expression profile analyses to compare the olfactory genes involved in the detection of sex pheromones. A total of 36 odorant-binding proteins (OBPs) and 52 olfactory receptors (ORs) were identified in . Phylogenetic analyses showed that EoblOBP2, 3, and 25 were grouped in the pheromone-binding protein clade with EgriOBP2, 3, 25, and another lepidopteran PBP. EoblOR25 and 28 were grouped with EgriOR25, 28, and pheromone receptors for the detection of Type-I sex pheromone components. EoblOR24, 31, 37, and 44 were grouped with EgriOR24, 31, 37, and 44. All of these 4 EoblORs and 4 showed higher abundance in male antennae than in female ones. Therefore, OBP2, 3, 25 and OR24, 31, 37, 44 of and might be responsible for sex pheromone component detection. However, the sequences of these genes in and were more than 90% identical. This indicates that these orthologous genes might play similar roles in the detection of sex pheromones. In contrast, the observed and differed in abundance between the antennae of the two species. Therefore, we speculate that these two species use the different transcript levels of PRs to differentiate sex pheromone components. The results of the present study might contribute in deciphering the mechanism for premating isolation in these species and may be of use in devising strategies for their management.
同胞物种[具体物种名1]和[具体物种名2]是中国主要的嚼食茶树害虫。性信息素成分的差异在这两个物种的交配前隔离中起着核心作用。为了研究这两个物种交配前隔离的机制,我们对雌性和雄性个体触角的转录组进行了测序,并进行了系统发育分析、丰度分析和组织表达谱分析,以比较参与检测性信息素的嗅觉基因。在[具体物种名1]中总共鉴定出36种气味结合蛋白(OBP)和52种嗅觉受体(OR)。系统发育分析表明,EoblOBP2、3和25与EgriOBP2、3、25以及另一种鳞翅目PBP归为信息素结合蛋白进化枝。EoblOR25和28与EgriOR25、28以及用于检测I型性信息素成分的信息素受体归为一组。EoblOR24、31、37和44与EgriOR24、31、37和44归为一组。所有这4种EoblOR和4种[具体物种名1]在雄性触角中的丰度均高于雌性触角。因此,[具体物种名1]和[具体物种名2]的OBP2、3、25以及OR24、31、37、44可能负责性信息素成分的检测。然而,[具体物种名1]和[具体物种名2]中这些基因的序列有90%以上相同。这表明这些直系同源基因在检测性信息素中可能发挥相似的作用。相比之下,可以观察到[具体物种名1]和[具体物种名2]在两个物种触角中的丰度存在差异。因此,我们推测这两个物种利用PRs的不同转录水平来区分性信息素成分。本研究结果可能有助于阐明这些物种交配前隔离的机制,并可能用于制定其管理策略。