{"title":"Functional characterization of Niemann-Pick proteins type C2 as odorant carriers in Neoseiulus barkeri olfactory perception.","authors":"Haozhuo Yang, Tiandi Niu, Rongjiang Ma, Dong Xiang, Huai Liu, Hanqiu Chen, Yaying Li","doi":"10.1111/1744-7917.70143","DOIUrl":null,"url":null,"abstract":"<p><p>Arthropods utilize olfactory function to detect informational substances within their natural habitats, thereby facilitating essential life activities such as foraging, mating, and oviposition. Niemann-Pick protein type C2 (NPC2), a putative odorant carrier, has not been fully described in the olfactory perception of predatory mites. In this study, we characterized in detail the olfactory perception functions of NbNPC2-2 and NbNPC2-3 in the important predatory mite Neoseiulus barkeri. The results show that 2 NPC2 proteins, with 6 conserved cysteine sites, are significantly upregulated (by 2.93-fold for NbNPC2-2 and 1.66-fold for NbNPC2-3) with methyl salicylate (MeSA), an important herbivore-induced plant volatile (HIPV). Knocking down both NbNPC2-2 and NbNPC2-3 prevented N. barkeri from preferring pest-infested plants, and reduced their crawling speed to 2.92 and 3.12 mm/s under MeSA treatment. The affinity analysis revealed that NPC2-2 binds to HIPVs β-ionone, MeSA, and ocimene (Ki = 28.55 ± 2.12, 40.73 ± 3.89, and 45.15 ± 2.22, respectively), and NPC2-3 binds to 4-ethylbenzaldehyde (Ki = 51.67 ± 0.23). Molecular docking further confirmed hydrogen bonding interactions between NPC2-2, NPC2-3, and these HIPVs. These results indicated that NPC2-2 and NPC2-3 act as odor carriers involved in the olfactory perception of mites toward HIPVs. This enhances understanding of the molecular mechanism of phytoseiid olfaction.</p>","PeriodicalId":13618,"journal":{"name":"Insect Science","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insect Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/1744-7917.70143","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Arthropods utilize olfactory function to detect informational substances within their natural habitats, thereby facilitating essential life activities such as foraging, mating, and oviposition. Niemann-Pick protein type C2 (NPC2), a putative odorant carrier, has not been fully described in the olfactory perception of predatory mites. In this study, we characterized in detail the olfactory perception functions of NbNPC2-2 and NbNPC2-3 in the important predatory mite Neoseiulus barkeri. The results show that 2 NPC2 proteins, with 6 conserved cysteine sites, are significantly upregulated (by 2.93-fold for NbNPC2-2 and 1.66-fold for NbNPC2-3) with methyl salicylate (MeSA), an important herbivore-induced plant volatile (HIPV). Knocking down both NbNPC2-2 and NbNPC2-3 prevented N. barkeri from preferring pest-infested plants, and reduced their crawling speed to 2.92 and 3.12 mm/s under MeSA treatment. The affinity analysis revealed that NPC2-2 binds to HIPVs β-ionone, MeSA, and ocimene (Ki = 28.55 ± 2.12, 40.73 ± 3.89, and 45.15 ± 2.22, respectively), and NPC2-3 binds to 4-ethylbenzaldehyde (Ki = 51.67 ± 0.23). Molecular docking further confirmed hydrogen bonding interactions between NPC2-2, NPC2-3, and these HIPVs. These results indicated that NPC2-2 and NPC2-3 act as odor carriers involved in the olfactory perception of mites toward HIPVs. This enhances understanding of the molecular mechanism of phytoseiid olfaction.
期刊介绍:
Insect Science is an English-language journal, which publishes original research articles dealing with all fields of research in into insects and other terrestrial arthropods. Papers in any of the following fields will be considered: ecology, behavior, biogeography, physiology, biochemistry, sociobiology, phylogeny, pest management, and exotic incursions. The emphasis of the journal is on the adaptation and evolutionary biology of insects from the molecular to the ecosystem level. Reviews, mini reviews and letters to the editor, book reviews, and information about academic activities of the society are also published.