Baculoviruses manipulate host lipid metabolism via adipokinetic hormone signaling to induce climbing behavior.

Baculoviruses can induce climbing behavior in caterpillar hosts, which provides an excellent model for studying parasite manipulation of host behavior. Herein, we found that Helicoverpa armigera single nucleopolyhedrovirus (HearNPV) promoted lipid metabolism of infected H. armigera larvae, and chang...

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Main Authors: Lin Zhu, Yuqing Xie, Chenxi Liu, Jie Cheng, Zhongjian Shen, Xiaoming Liu, Limei Cai, Xinyuan Ning, Songdou Zhang, Zhen Li, Qiuying Huang, Xiaoxia Liu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2025-01-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1012932
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author Lin Zhu
Yuqing Xie
Chenxi Liu
Jie Cheng
Zhongjian Shen
Xiaoming Liu
Limei Cai
Xinyuan Ning
Songdou Zhang
Zhen Li
Qiuying Huang
Xiaoxia Liu
author_facet Lin Zhu
Yuqing Xie
Chenxi Liu
Jie Cheng
Zhongjian Shen
Xiaoming Liu
Limei Cai
Xinyuan Ning
Songdou Zhang
Zhen Li
Qiuying Huang
Xiaoxia Liu
author_sort Lin Zhu
collection DOAJ
description Baculoviruses can induce climbing behavior in caterpillar hosts, which provides an excellent model for studying parasite manipulation of host behavior. Herein, we found that Helicoverpa armigera single nucleopolyhedrovirus (HearNPV) promoted lipid metabolism of infected H. armigera larvae, and changes in lipid metabolism can affect climbing behavior. Therefore, understanding the molecular mechanisms between lipid metabolism and climbing behavior is particularly important. In this study, we found adipokinetic hormone 1 (HaAKH1), adipokinetic hormone 2 (HaAKH2) and their receptor HaAKHR were essential for promoting lipid metabolism and climbing behavior in response to HearNPV infection. Both molecular docking result and Ca2+ imaging showed that both HaAKH1 and HaAKH2 could interact with HaAKHR. Knockdown of HaAKH1, HaAKH2 and HaAKHR resulted in not only the accumulation of triacylglycerol (TAG), but also the reduction of the replication of HearNPV and the crawling ability of infected H. armigera larvae, resulting in a decrease in the final death height of the infected larvae. We further validated this conclusion by injecting active peptides of HaAKH1 and HaAKH2 to infected larvae. In addition, we investigated the downstream of HaAKH signaling and found that hormone-sensitive lipase (HaHSL) changed with changes in HaAKH signaling and HaHSL played the same role as HaAKH signaling. These findings not only revealed the mechanism by which parasites manipulated host lipid metabolism, but more significantly, explored the relationship between lipid metabolism and behavioral changes of hosts manipulated by parasites, broadening our understanding of the phenomenon of parasites manipulating host behavioral changes.
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spelling doaj-art-24977d5b0db34a8db14cf1d51974e8ff2025-08-20T03:48:51ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742025-01-01211e101293210.1371/journal.ppat.1012932Baculoviruses manipulate host lipid metabolism via adipokinetic hormone signaling to induce climbing behavior.Lin ZhuYuqing XieChenxi LiuJie ChengZhongjian ShenXiaoming LiuLimei CaiXinyuan NingSongdou ZhangZhen LiQiuying HuangXiaoxia LiuBaculoviruses can induce climbing behavior in caterpillar hosts, which provides an excellent model for studying parasite manipulation of host behavior. Herein, we found that Helicoverpa armigera single nucleopolyhedrovirus (HearNPV) promoted lipid metabolism of infected H. armigera larvae, and changes in lipid metabolism can affect climbing behavior. Therefore, understanding the molecular mechanisms between lipid metabolism and climbing behavior is particularly important. In this study, we found adipokinetic hormone 1 (HaAKH1), adipokinetic hormone 2 (HaAKH2) and their receptor HaAKHR were essential for promoting lipid metabolism and climbing behavior in response to HearNPV infection. Both molecular docking result and Ca2+ imaging showed that both HaAKH1 and HaAKH2 could interact with HaAKHR. Knockdown of HaAKH1, HaAKH2 and HaAKHR resulted in not only the accumulation of triacylglycerol (TAG), but also the reduction of the replication of HearNPV and the crawling ability of infected H. armigera larvae, resulting in a decrease in the final death height of the infected larvae. We further validated this conclusion by injecting active peptides of HaAKH1 and HaAKH2 to infected larvae. In addition, we investigated the downstream of HaAKH signaling and found that hormone-sensitive lipase (HaHSL) changed with changes in HaAKH signaling and HaHSL played the same role as HaAKH signaling. These findings not only revealed the mechanism by which parasites manipulated host lipid metabolism, but more significantly, explored the relationship between lipid metabolism and behavioral changes of hosts manipulated by parasites, broadening our understanding of the phenomenon of parasites manipulating host behavioral changes.https://doi.org/10.1371/journal.ppat.1012932
spellingShingle Lin Zhu
Yuqing Xie
Chenxi Liu
Jie Cheng
Zhongjian Shen
Xiaoming Liu
Limei Cai
Xinyuan Ning
Songdou Zhang
Zhen Li
Qiuying Huang
Xiaoxia Liu
Baculoviruses manipulate host lipid metabolism via adipokinetic hormone signaling to induce climbing behavior.
PLoS Pathogens
title Baculoviruses manipulate host lipid metabolism via adipokinetic hormone signaling to induce climbing behavior.
title_full Baculoviruses manipulate host lipid metabolism via adipokinetic hormone signaling to induce climbing behavior.
title_fullStr Baculoviruses manipulate host lipid metabolism via adipokinetic hormone signaling to induce climbing behavior.
title_full_unstemmed Baculoviruses manipulate host lipid metabolism via adipokinetic hormone signaling to induce climbing behavior.
title_short Baculoviruses manipulate host lipid metabolism via adipokinetic hormone signaling to induce climbing behavior.
title_sort baculoviruses manipulate host lipid metabolism via adipokinetic hormone signaling to induce climbing behavior
url https://doi.org/10.1371/journal.ppat.1012932
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