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A novel physiological function of pheromone biosynthesis-activating neuropeptide in production of aggregation pheromone

The western flower thrips, Frankliniella occidentalis, is an insect pest, and its aggregation pheromone (AP) plays a crucial role in the recruitment of both sexes. A novel pheromone biosynthesis-activating neuropeptide (PBAN)-like gene is encoded in F. occidentalis genome, but its physiological func...

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Autores principales: Khan, Falguni, Kim, Keono, Sung, Jeehye, Lim, Hangah, Kim, Sang-Gyu, Choi, Man-Yeon, Kim, Yonggyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076286/
https://www.ncbi.nlm.nih.gov/pubmed/37019976
http://dx.doi.org/10.1038/s41598-023-32833-9
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author Khan, Falguni
Kim, Keono
Sung, Jeehye
Lim, Hangah
Kim, Sang-Gyu
Choi, Man-Yeon
Kim, Yonggyun
author_facet Khan, Falguni
Kim, Keono
Sung, Jeehye
Lim, Hangah
Kim, Sang-Gyu
Choi, Man-Yeon
Kim, Yonggyun
author_sort Khan, Falguni
collection PubMed
description The western flower thrips, Frankliniella occidentalis, is an insect pest, and its aggregation pheromone (AP) plays a crucial role in the recruitment of both sexes. A novel pheromone biosynthesis-activating neuropeptide (PBAN)-like gene is encoded in F. occidentalis genome, but its physiological function has yet to be elucidated. This study hypothesized the physiological role played by PBAN in mediating AP production. AP has been known to be produced only by male adults in F. occidentalis. Surprisingly, our extraction of headspace volatiles contained two AP components in females as well as in males with similar composition. PBAN injection elevated the AP production whereas RNA interference (RNAi) of the gene expression suppressed the AP production in both sexes. A biosynthetic pathway to produce AP components were predicted and the enzymes catalyzing the main steps were confirmed in their expressions. Individual RNAi treatments of these genes significantly suppressed AP production. RNAi of PBAN gene downregulated the expressions of these biosynthesis-associated genes in both sexes. These results suggest that the novel neuropeptide acts as PBAN mediating AP production through stimulating its biosynthetic machinery in F. occidentalis.
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spelling pubmed-100762862023-04-07 A novel physiological function of pheromone biosynthesis-activating neuropeptide in production of aggregation pheromone Khan, Falguni Kim, Keono Sung, Jeehye Lim, Hangah Kim, Sang-Gyu Choi, Man-Yeon Kim, Yonggyun Sci Rep Article The western flower thrips, Frankliniella occidentalis, is an insect pest, and its aggregation pheromone (AP) plays a crucial role in the recruitment of both sexes. A novel pheromone biosynthesis-activating neuropeptide (PBAN)-like gene is encoded in F. occidentalis genome, but its physiological function has yet to be elucidated. This study hypothesized the physiological role played by PBAN in mediating AP production. AP has been known to be produced only by male adults in F. occidentalis. Surprisingly, our extraction of headspace volatiles contained two AP components in females as well as in males with similar composition. PBAN injection elevated the AP production whereas RNA interference (RNAi) of the gene expression suppressed the AP production in both sexes. A biosynthetic pathway to produce AP components were predicted and the enzymes catalyzing the main steps were confirmed in their expressions. Individual RNAi treatments of these genes significantly suppressed AP production. RNAi of PBAN gene downregulated the expressions of these biosynthesis-associated genes in both sexes. These results suggest that the novel neuropeptide acts as PBAN mediating AP production through stimulating its biosynthetic machinery in F. occidentalis. Nature Publishing Group UK 2023-04-05 /pmc/articles/PMC10076286/ /pubmed/37019976 http://dx.doi.org/10.1038/s41598-023-32833-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Khan, Falguni
Kim, Keono
Sung, Jeehye
Lim, Hangah
Kim, Sang-Gyu
Choi, Man-Yeon
Kim, Yonggyun
A novel physiological function of pheromone biosynthesis-activating neuropeptide in production of aggregation pheromone
title A novel physiological function of pheromone biosynthesis-activating neuropeptide in production of aggregation pheromone
title_full A novel physiological function of pheromone biosynthesis-activating neuropeptide in production of aggregation pheromone
title_fullStr A novel physiological function of pheromone biosynthesis-activating neuropeptide in production of aggregation pheromone
title_full_unstemmed A novel physiological function of pheromone biosynthesis-activating neuropeptide in production of aggregation pheromone
title_short A novel physiological function of pheromone biosynthesis-activating neuropeptide in production of aggregation pheromone
title_sort novel physiological function of pheromone biosynthesis-activating neuropeptide in production of aggregation pheromone
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076286/
https://www.ncbi.nlm.nih.gov/pubmed/37019976
http://dx.doi.org/10.1038/s41598-023-32833-9
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