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Search performance and octopamine neuronal signaling mediate parasitoid induced changes in Drosophila oviposition behavior
Making the appropriate responses to predation risk is essential for the survival of an organism; however, the underlying mechanisms are still largely unknown. Here, we find that Drosophila has evolved an adaptive strategy to manage the threat from its parasitoid wasp by manipulating the oviposition...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345866/ https://www.ncbi.nlm.nih.gov/pubmed/35918358 http://dx.doi.org/10.1038/s41467-022-32203-5 |
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author | Pang, Lan Liu, Zhiguo Chen, Jiani Dong, Zhi Zhou, Sicong Zhang, Qichao Lu, Yueqi Sheng, Yifeng Chen, Xuexin Huang, Jianhua |
author_facet | Pang, Lan Liu, Zhiguo Chen, Jiani Dong, Zhi Zhou, Sicong Zhang, Qichao Lu, Yueqi Sheng, Yifeng Chen, Xuexin Huang, Jianhua |
author_sort | Pang, Lan |
collection | PubMed |
description | Making the appropriate responses to predation risk is essential for the survival of an organism; however, the underlying mechanisms are still largely unknown. Here, we find that Drosophila has evolved an adaptive strategy to manage the threat from its parasitoid wasp by manipulating the oviposition behavior. Through perception of the differences in host search performance of wasps, Drosophila is able to recognize younger wasps as a higher level of threat and consequently depress the oviposition. We further show that this antiparasitoid behavior is mediated by the regulation of the expression of Tdc2 and Tβh in the ventral nerve cord via LC4 visual projection neurons, which in turn leads to the dramatic reduction in octopamine and the resulting dysfunction of mature follicle trimming and rupture. Our study uncovers a detailed mechanism underlying the defensive behavior in insects that may advance our understanding of predator avoidance in animals. |
format | Online Article Text |
id | pubmed-9345866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93458662022-08-04 Search performance and octopamine neuronal signaling mediate parasitoid induced changes in Drosophila oviposition behavior Pang, Lan Liu, Zhiguo Chen, Jiani Dong, Zhi Zhou, Sicong Zhang, Qichao Lu, Yueqi Sheng, Yifeng Chen, Xuexin Huang, Jianhua Nat Commun Article Making the appropriate responses to predation risk is essential for the survival of an organism; however, the underlying mechanisms are still largely unknown. Here, we find that Drosophila has evolved an adaptive strategy to manage the threat from its parasitoid wasp by manipulating the oviposition behavior. Through perception of the differences in host search performance of wasps, Drosophila is able to recognize younger wasps as a higher level of threat and consequently depress the oviposition. We further show that this antiparasitoid behavior is mediated by the regulation of the expression of Tdc2 and Tβh in the ventral nerve cord via LC4 visual projection neurons, which in turn leads to the dramatic reduction in octopamine and the resulting dysfunction of mature follicle trimming and rupture. Our study uncovers a detailed mechanism underlying the defensive behavior in insects that may advance our understanding of predator avoidance in animals. Nature Publishing Group UK 2022-08-02 /pmc/articles/PMC9345866/ /pubmed/35918358 http://dx.doi.org/10.1038/s41467-022-32203-5 Text en © The Author(s) 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Pang, Lan Liu, Zhiguo Chen, Jiani Dong, Zhi Zhou, Sicong Zhang, Qichao Lu, Yueqi Sheng, Yifeng Chen, Xuexin Huang, Jianhua Search performance and octopamine neuronal signaling mediate parasitoid induced changes in Drosophila oviposition behavior |
title | Search performance and octopamine neuronal signaling mediate parasitoid induced changes in Drosophila oviposition behavior |
title_full | Search performance and octopamine neuronal signaling mediate parasitoid induced changes in Drosophila oviposition behavior |
title_fullStr | Search performance and octopamine neuronal signaling mediate parasitoid induced changes in Drosophila oviposition behavior |
title_full_unstemmed | Search performance and octopamine neuronal signaling mediate parasitoid induced changes in Drosophila oviposition behavior |
title_short | Search performance and octopamine neuronal signaling mediate parasitoid induced changes in Drosophila oviposition behavior |
title_sort | search performance and octopamine neuronal signaling mediate parasitoid induced changes in drosophila oviposition behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345866/ https://www.ncbi.nlm.nih.gov/pubmed/35918358 http://dx.doi.org/10.1038/s41467-022-32203-5 |
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