Trait responses, nonconsumptive effects, and the physiological basis of Helicoverpa armigera to bat predation risk

Abstract Predation reduces the population density of prey, affecting its fitness and population dynamics. Few studies have connected trait changes with fitness consequences in prey and the molecular basis and metabolic mechanisms of such changes in bat-insect systems. This study focuses on the respo...

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Main Authors: Yingying Liu, Yang Geng, Man Si, Dan Zhu, Zhenglanyi Huang, Hanli Yin, Hao Zeng, Jiang Feng, Tinglei Jiang
Format: Article
Language:English
Published: Nature Portfolio 2024-11-01
Series:Communications Biology
Online Access:https://doi.org/10.1038/s42003-024-07166-6
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author Yingying Liu
Yang Geng
Man Si
Dan Zhu
Zhenglanyi Huang
Hanli Yin
Hao Zeng
Jiang Feng
Tinglei Jiang
author_facet Yingying Liu
Yang Geng
Man Si
Dan Zhu
Zhenglanyi Huang
Hanli Yin
Hao Zeng
Jiang Feng
Tinglei Jiang
author_sort Yingying Liu
collection DOAJ
description Abstract Predation reduces the population density of prey, affecting its fitness and population dynamics. Few studies have connected trait changes with fitness consequences in prey and the molecular basis and metabolic mechanisms of such changes in bat-insect systems. This study focuses on the responses of Helicoverpa armigera to different predation risks, focusing on echolocating bats and their calls. Substantial modifications were observed in the nocturnal and diurnal activities of H. armigera under predation risk, with enhanced evasion behaviors. Accelerated development and decreased fitness were observed under predation risks. Transcriptomic and metabolomic analyses indicated that exposure to bats induced the upregulation of amino acid metabolism- and antioxidant pathway-related genes, reflecting shifts in resource utilization in response to oxidative stress. Exposure to bat predation risks enhanced the activity of DNA damage repair pathways and suppressed energy metabolism, contributing to the observed trait changes and fitness decreases. The current results underscore the complex adaptive strategies that prey species evolve in response to predation risk, enhancing our understanding of the predator–prey dynamic and offering valuable insights for innovative and ecologically informed pest management strategies.
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publisher Nature Portfolio
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spelling doaj-art-0209508231c24e5c8bc6dda2e5c44bd42024-11-10T12:39:25ZengNature PortfolioCommunications Biology2399-36422024-11-017111410.1038/s42003-024-07166-6Trait responses, nonconsumptive effects, and the physiological basis of Helicoverpa armigera to bat predation riskYingying Liu0Yang Geng1Man Si2Dan Zhu3Zhenglanyi Huang4Hanli Yin5Hao Zeng6Jiang Feng7Tinglei Jiang8Jilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal UniversityJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal UniversityJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal UniversityJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal UniversityJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal UniversityJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal UniversityJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal UniversityJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal UniversityJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal UniversityAbstract Predation reduces the population density of prey, affecting its fitness and population dynamics. Few studies have connected trait changes with fitness consequences in prey and the molecular basis and metabolic mechanisms of such changes in bat-insect systems. This study focuses on the responses of Helicoverpa armigera to different predation risks, focusing on echolocating bats and their calls. Substantial modifications were observed in the nocturnal and diurnal activities of H. armigera under predation risk, with enhanced evasion behaviors. Accelerated development and decreased fitness were observed under predation risks. Transcriptomic and metabolomic analyses indicated that exposure to bats induced the upregulation of amino acid metabolism- and antioxidant pathway-related genes, reflecting shifts in resource utilization in response to oxidative stress. Exposure to bat predation risks enhanced the activity of DNA damage repair pathways and suppressed energy metabolism, contributing to the observed trait changes and fitness decreases. The current results underscore the complex adaptive strategies that prey species evolve in response to predation risk, enhancing our understanding of the predator–prey dynamic and offering valuable insights for innovative and ecologically informed pest management strategies.https://doi.org/10.1038/s42003-024-07166-6
spellingShingle Yingying Liu
Yang Geng
Man Si
Dan Zhu
Zhenglanyi Huang
Hanli Yin
Hao Zeng
Jiang Feng
Tinglei Jiang
Trait responses, nonconsumptive effects, and the physiological basis of Helicoverpa armigera to bat predation risk
Communications Biology
title Trait responses, nonconsumptive effects, and the physiological basis of Helicoverpa armigera to bat predation risk
title_full Trait responses, nonconsumptive effects, and the physiological basis of Helicoverpa armigera to bat predation risk
title_fullStr Trait responses, nonconsumptive effects, and the physiological basis of Helicoverpa armigera to bat predation risk
title_full_unstemmed Trait responses, nonconsumptive effects, and the physiological basis of Helicoverpa armigera to bat predation risk
title_short Trait responses, nonconsumptive effects, and the physiological basis of Helicoverpa armigera to bat predation risk
title_sort trait responses nonconsumptive effects and the physiological basis of helicoverpa armigera to bat predation risk
url https://doi.org/10.1038/s42003-024-07166-6
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