Aquaporins modulate the cold response of Haemaphysalis longicornis via changes in gene and protein expression of fatty acids

Abstract Background As ectotherms that spend most of their life in the environment (off-host), ticks face challenges in maintaining water balance, and some species must cope with severe low winter temperatures. Aquaporins (AQPs) are essential membrane proteins that enhance cold tolerance in many ani...

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Main Authors: Han Wang, Ruwei Bai, Tingwei Pei, Jianglei Meng, Chuks F. Nwanade, Yuchao Zhang, Xiujie Liang, Yunsheng Tang, Jingze Liu, Zhijun Yu
Format: Article
Language:English
Published: BMC 2025-02-01
Series:Parasites & Vectors
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Online Access:https://doi.org/10.1186/s13071-025-06718-x
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author Han Wang
Ruwei Bai
Tingwei Pei
Jianglei Meng
Chuks F. Nwanade
Yuchao Zhang
Xiujie Liang
Yunsheng Tang
Jingze Liu
Zhijun Yu
author_facet Han Wang
Ruwei Bai
Tingwei Pei
Jianglei Meng
Chuks F. Nwanade
Yuchao Zhang
Xiujie Liang
Yunsheng Tang
Jingze Liu
Zhijun Yu
author_sort Han Wang
collection DOAJ
description Abstract Background As ectotherms that spend most of their life in the environment (off-host), ticks face challenges in maintaining water balance, and some species must cope with severe low winter temperatures. Aquaporins (AQPs) are essential membrane proteins that enhance cold tolerance in many animals by regulating homeostatic processes. However, the dynamic expressions and involvement of aquaporins in the cold stress of ticks remain unclear. Methods In the present study, three AQP genes, HlAQP2, HlAQP3, and HlAQP5, belonging to the major intrinsic protein (MIP) superfamily, were characterized from the important vector tick Haemaphysalis longicornis. Then, multiple bioinformatics analyses were performed. Quantitative real-time PCR (qPCR) was used to detect different expressions of H. longicornis genes under different cold treatment conditions. RNA interference was used to explore the relationship between AQP and the cold response of H. longicornis. Additionally, proteomic and transcriptomic analyses were used to investigate the mechanisms underlying the effects of AQPs on cold response in ticks. Results The amino acid sequence of AQPs shows high homology in Ixodida, with HlAQP2 and HlAQP5 proteins comprising two asparagine-proline-alanine (NPA) motifs, whereas HlAQP3 protein was featured by glycerol facilitator GlpF channel. The spatiotemporal expression of AQPs in H. longicornis varied significantly after low temperature treatment, and different expression patterns were observed over prolonged exposure periods. RNAi knockdown of AQPs significantly increased tick mortality after treatment at a sublethal temperature of − 14 °C for 2 h. Proteomic and transcriptomic analysis revealed that the differentially expressed genes and proteins caused by the knockdown of AQPs are mainly enriched in the fatty acid metabolism pathway. Conclusions The above results indicated that AQPs could regulate tick cold response by modulating water balance and fatty acid metabolism. Graphical Abstract
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spelling doaj-art-588ab867f8bc48258f7048c4f20a40fc2025-08-20T02:01:35ZengBMCParasites & Vectors1756-33052025-02-0118111510.1186/s13071-025-06718-xAquaporins modulate the cold response of Haemaphysalis longicornis via changes in gene and protein expression of fatty acidsHan Wang0Ruwei Bai1Tingwei Pei2Jianglei Meng3Chuks F. Nwanade4Yuchao Zhang5Xiujie Liang6Yunsheng Tang7Jingze Liu8Zhijun Yu9Hebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Research Center of the Basic Discipline of Cell Biology, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Sciences, Hebei Normal UniversityHebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Research Center of the Basic Discipline of Cell Biology, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Sciences, Hebei Normal UniversityHebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Research Center of the Basic Discipline of Cell Biology, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Sciences, Hebei Normal UniversityHebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Research Center of the Basic Discipline of Cell Biology, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Sciences, Hebei Normal UniversityGuangdong Key Laboratory of Animal Conservation and Resource Utilization, Guangdong Public Laboratory of Wild Animal Conservation and Utilization, Institute of Zoology, Guangdong Academy of SciencesHebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Research Center of the Basic Discipline of Cell Biology, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Sciences, Hebei Normal UniversityHebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Research Center of the Basic Discipline of Cell Biology, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Sciences, Hebei Normal UniversityHebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Research Center of the Basic Discipline of Cell Biology, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Sciences, Hebei Normal UniversityHebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Research Center of the Basic Discipline of Cell Biology, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Sciences, Hebei Normal UniversityHebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Research Center of the Basic Discipline of Cell Biology, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Sciences, Hebei Normal UniversityAbstract Background As ectotherms that spend most of their life in the environment (off-host), ticks face challenges in maintaining water balance, and some species must cope with severe low winter temperatures. Aquaporins (AQPs) are essential membrane proteins that enhance cold tolerance in many animals by regulating homeostatic processes. However, the dynamic expressions and involvement of aquaporins in the cold stress of ticks remain unclear. Methods In the present study, three AQP genes, HlAQP2, HlAQP3, and HlAQP5, belonging to the major intrinsic protein (MIP) superfamily, were characterized from the important vector tick Haemaphysalis longicornis. Then, multiple bioinformatics analyses were performed. Quantitative real-time PCR (qPCR) was used to detect different expressions of H. longicornis genes under different cold treatment conditions. RNA interference was used to explore the relationship between AQP and the cold response of H. longicornis. Additionally, proteomic and transcriptomic analyses were used to investigate the mechanisms underlying the effects of AQPs on cold response in ticks. Results The amino acid sequence of AQPs shows high homology in Ixodida, with HlAQP2 and HlAQP5 proteins comprising two asparagine-proline-alanine (NPA) motifs, whereas HlAQP3 protein was featured by glycerol facilitator GlpF channel. The spatiotemporal expression of AQPs in H. longicornis varied significantly after low temperature treatment, and different expression patterns were observed over prolonged exposure periods. RNAi knockdown of AQPs significantly increased tick mortality after treatment at a sublethal temperature of − 14 °C for 2 h. Proteomic and transcriptomic analysis revealed that the differentially expressed genes and proteins caused by the knockdown of AQPs are mainly enriched in the fatty acid metabolism pathway. Conclusions The above results indicated that AQPs could regulate tick cold response by modulating water balance and fatty acid metabolism. Graphical Abstracthttps://doi.org/10.1186/s13071-025-06718-xHaemaphysalis longicornisAquaporinCold responseWater balanceFatty acid metabolism
spellingShingle Han Wang
Ruwei Bai
Tingwei Pei
Jianglei Meng
Chuks F. Nwanade
Yuchao Zhang
Xiujie Liang
Yunsheng Tang
Jingze Liu
Zhijun Yu
Aquaporins modulate the cold response of Haemaphysalis longicornis via changes in gene and protein expression of fatty acids
Parasites & Vectors
Haemaphysalis longicornis
Aquaporin
Cold response
Water balance
Fatty acid metabolism
title Aquaporins modulate the cold response of Haemaphysalis longicornis via changes in gene and protein expression of fatty acids
title_full Aquaporins modulate the cold response of Haemaphysalis longicornis via changes in gene and protein expression of fatty acids
title_fullStr Aquaporins modulate the cold response of Haemaphysalis longicornis via changes in gene and protein expression of fatty acids
title_full_unstemmed Aquaporins modulate the cold response of Haemaphysalis longicornis via changes in gene and protein expression of fatty acids
title_short Aquaporins modulate the cold response of Haemaphysalis longicornis via changes in gene and protein expression of fatty acids
title_sort aquaporins modulate the cold response of haemaphysalis longicornis via changes in gene and protein expression of fatty acids
topic Haemaphysalis longicornis
Aquaporin
Cold response
Water balance
Fatty acid metabolism
url https://doi.org/10.1186/s13071-025-06718-x
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