Identification of odorant-binding proteins in Ceutorhynchus asper and functional analyses of CaspOBP9.

IF 3.8 1区 农林科学 Q1 AGRONOMY
Xinghao Li,Fangjing Hu,Rufan Li,Danhao Peng,Ping Gao,Fuqiang Rao,Abdul Ghaffar Khoso,Yonghong Li,Deguang Liu
{"title":"Identification of odorant-binding proteins in Ceutorhynchus asper and functional analyses of CaspOBP9.","authors":"Xinghao Li,Fangjing Hu,Rufan Li,Danhao Peng,Ping Gao,Fuqiang Rao,Abdul Ghaffar Khoso,Yonghong Li,Deguang Liu","doi":"10.1002/ps.70252","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nThe rape stem weevil (Ceutorhynchus asper) represents a significant threat to economically-important cruciferous crops. The main aim was to characterize CaspOBPs (odorant-binding proteins) and the functions of CaspOBP9.\r\n\r\nRESULTS\r\nWe performed transcriptomic sequencing on C. asper tissues and identified 21 CaspOBPs. A majority of CaspOBPs were relatively highly expressed in the antennae; for these OBPs, CaspOBP9, 12, 16, 19 and 20 were female-biased, whereas CaspOBP5, 8 and 10 were male-biased. Recombinant CaspOBP9 showed good affinity for four plant volatiles and two pesticides, suggesting that CaspOBP9 was involved in perception of both pesticides and host volatiles. Behavioral experiments showed that C. asper was significantly attracted to decanal, benzyl isothiocyanate (ITC) and phenylethyl isothiocyanate. Molecular simulations suggest that Van der Waals forces serve as the main driving force for the formation of CaspOBP9-ligand complexes. Residues LEU:71, THR:79 and TYR:105 were identified to be critical in the formation of the complexes. Site-directed mutagenesis experiments showed that mutated proteins at the above-mentioned three sites had reduced or even no binding affinity for the corresponding compounds. RNAi experiments targeting CaspOBP9 confirmed its essential roles in olfactory perception of C. asper.\r\n\r\nCONCLUSIONS\r\nCaspOBP9 could play important roles in perception of particular plant volatiles (e.g. benzyl ITC) and pesticides (e.g. chlorpyrifos) by C. asper, and its key residues LEU:71, THR:79 and TYR:105 were identified. This research provides valuable insights into the molecular mechanisms underlying olfactory perception of C. asper, and a foundation for the development of novel control techniques for this weevil. © 2025 Society of Chemical Industry.","PeriodicalId":218,"journal":{"name":"Pest Management Science","volume":"6 1","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pest Management Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1002/ps.70252","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRONOMY","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND The rape stem weevil (Ceutorhynchus asper) represents a significant threat to economically-important cruciferous crops. The main aim was to characterize CaspOBPs (odorant-binding proteins) and the functions of CaspOBP9. RESULTS We performed transcriptomic sequencing on C. asper tissues and identified 21 CaspOBPs. A majority of CaspOBPs were relatively highly expressed in the antennae; for these OBPs, CaspOBP9, 12, 16, 19 and 20 were female-biased, whereas CaspOBP5, 8 and 10 were male-biased. Recombinant CaspOBP9 showed good affinity for four plant volatiles and two pesticides, suggesting that CaspOBP9 was involved in perception of both pesticides and host volatiles. Behavioral experiments showed that C. asper was significantly attracted to decanal, benzyl isothiocyanate (ITC) and phenylethyl isothiocyanate. Molecular simulations suggest that Van der Waals forces serve as the main driving force for the formation of CaspOBP9-ligand complexes. Residues LEU:71, THR:79 and TYR:105 were identified to be critical in the formation of the complexes. Site-directed mutagenesis experiments showed that mutated proteins at the above-mentioned three sites had reduced or even no binding affinity for the corresponding compounds. RNAi experiments targeting CaspOBP9 confirmed its essential roles in olfactory perception of C. asper. CONCLUSIONS CaspOBP9 could play important roles in perception of particular plant volatiles (e.g. benzyl ITC) and pesticides (e.g. chlorpyrifos) by C. asper, and its key residues LEU:71, THR:79 and TYR:105 were identified. This research provides valuable insights into the molecular mechanisms underlying olfactory perception of C. asper, and a foundation for the development of novel control techniques for this weevil. © 2025 Society of Chemical Industry.
山雀气味结合蛋白鉴定及CaspOBP9功能分析。
油菜茎象甲(Ceutorhynchus asper)对经济上重要的十字花科作物构成严重威胁。主要目的是表征CaspOBPs(气味结合蛋白)和CaspOBP9的功能。结果对紫杉组织进行转录组测序,鉴定出21个caspobp。大部分caspobp在触角中相对高表达;对于这些OBPs, CaspOBP9、12、16、19和20是女性偏倚的,而CaspOBP5、8和10是男性偏倚的。重组CaspOBP9对4种植物挥发物和2种农药具有良好的亲和性,表明CaspOBP9参与了农药和寄主挥发物的感知。行为学实验表明,蔓越莓对癸醛、异硫氰酸苄酯和异硫氰酸苯乙基均有显著的吸引作用。分子模拟表明,范德华力是caspobp9配体复合物形成的主要驱动力。残基LEU:71, THR:79和TYR:105被鉴定为复合物形成的关键。定点诱变实验表明,上述三个位点的突变蛋白对相应化合物的结合亲和力降低,甚至没有结合亲和力。以CaspOBP9为靶点的RNAi实验证实了其在紫杉嗅觉感知中的重要作用。结论scaspobp9可能在紫杉对特定植物挥发物(如苯ITC)和农药(如毒死蜱)的感知中起重要作用,鉴定出其关键残留LEU:71、THR:79和TYR:105。本研究为揭示小象嗅觉的分子机制提供了有价值的见解,并为开发新的控制技术奠定了基础。©2025化学工业协会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Pest Management Science
Pest Management Science 农林科学-昆虫学
CiteScore
7.90
自引率
9.80%
发文量
553
审稿时长
4.8 months
期刊介绍: Pest Management Science is the international journal of research and development in crop protection and pest control. Since its launch in 1970, the journal has become the premier forum for papers on the discovery, application, and impact on the environment of products and strategies designed for pest management. Published for SCI by John Wiley & Sons Ltd.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信