| Title: | Contribution of odorant binding proteins to olfactory detection of (Z)-11-hexadecenal in Helicoverpa armigera |
| Author(s): | Guo H; Guo PP; Sun YL; Huang LQ; Wang CZ; |
| Address: | "State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, PR China; CAS Center for Excellence in Biotic Interactions, University of Chinese Academy of Sciences, Beijing, PR China. State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, PR China; Forest College, Henan University of Science and Technology, Luoyang, PR China. State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, PR China. State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, PR China; CAS Center for Excellence in Biotic Interactions, University of Chinese Academy of Sciences, Beijing, PR China. Electronic address: czwang@ioz.ac.cn" |
| DOI: | 10.1016/j.ibmb.2021.103554 |
| ISSN/ISBN: | 1879-0240 (Electronic) 0965-1748 (Linking) |
| Abstract: | "Helicoverpa armigera utilizes (Z)-11-hexadecenal (Z11-16:Ald) as its major sex pheromone component. Three pheromone binding proteins (PBPs) and two general odorant binding proteins (GOBPs) are abundantly expressed in the male antennae of H. armigera. However, their precise roles in the olfactory detection of Z11-16:Ald remain enigmatic. To answer this question, we first synthesized the antibody against HarmOR13, an olfactory receptor (OR) primarily responding to Z11-16:Ald and mapped the local associations between PBPs/GOBPs and HarmOR13. Immunostaining showed that HarmPBPs and HarmGOBPs were localized in the supporting cells of trichoid sensilla and basiconic sensilla respectively. In particular, HarmPBP1 and HarmPBP2 were colocalized in the cells surrounding the olfactory receptor neurons (ORNs) expressing HarmOR13. Next, using two noninterfering binary expression tools, we heterologously expressed HarmPBP1, HarmPBP2 and HarmOR13 in Drosophila T1 sensilla to validate the functional interplay between PBPs and HarmOR13. We found that the addition of HarmPBP1 or HarmPBP2, not HarmPBP3, significantly increased HarmOR13's response to Z11-16:Ald. However, the presence of either HarmPBP1 or HarmPBP2 was ineffective to change the tuning breadth of HarmOR13 and modulate the response kinetics of this receptor. Taken together, this work demonstrates both HarmPBP1 and HarmPBP2 are involved in Z11-16:Ald detection. Our results support the idea that PBPs can contribute to the peripheral olfactory sensitivity but do little in modulating the selectivity and the response kinetics of corresponding ORs" |
| Keywords: | "Aldehydes/*pharmacology Animals Antibodies Arthropod Antennae/metabolism Immunohistochemistry/methods Insect Proteins/metabolism Moths/*metabolism/physiology Olfactory Receptor Neurons/physiology Receptors, Odorant/drug effects/immunology/*metabolism Sens;" |
| Notes: | "MedlineGuo, Hao Guo, Ping-Ping Sun, Ya-Lan Huang, Ling-Qiao Wang, Chen-Zhu eng Research Support, Non-U.S. Gov't England 2021/02/19 Insect Biochem Mol Biol. 2021 Apr; 131:103554. doi: 10.1016/j.ibmb.2021.103554. Epub 2021 Feb 15" |
