Duo Wang, Hongxia Li, Xiaojing Zhang, Xuanxuan Wang, Xiaohan Di, Zhijun Yu, Fang Wang, Yankai Zhang, Jingze Liu
{"title":"转铁蛋白影响长角血蜱的食物摄取和繁殖","authors":"Duo Wang, Hongxia Li, Xiaojing Zhang, Xuanxuan Wang, Xiaohan Di, Zhijun Yu, Fang Wang, Yankai Zhang, Jingze Liu","doi":"10.1127/entomologia/2023/2065","DOIUrl":null,"url":null,"abstract":"Transferrin (Tsf) is an extracellular protein with a high affinity for iron in vertebrates, but its function and mechanism in ticks are poorly understood. This study investigated Tsf in the hard tick Haemaphysalis longicornis Neumann (Ixodida: Ixodidae) for the first time. The results showed that Tsf was expressed in three developmental stages (larva, nymph, and female) and in various tissues (salivary glands, ovary, midgut, and Malpighian tubules), with higher expression levels observed after a blood meal. Using the Escherichia coli expression system, it was revealed that the hard tick Tsf protein exhibited iron chelation, radical-scavenging, antibacterial, and hemolytic activities in vitro. Silencing Tsf using RNA interference (RNAi) had adverse effects on the feeding ability and reproduction of H. longicornis, resulting in decreased engorgement weight, ovary weight, egg mass weight, egg hatching rate as well as a prolonged incubation period of eggs from oviposition to larvae hatching. Additionally, proteomics was used to investigate the mechanisms underlying the effects of Tsf on food intake and reproduction in H. longicornis females. The results revealed that Tsf may affect these processes through various pathways, including the ubiquitin–proteasome pathway, lipid metabolic pathways, carbohydrate metabolic pathways, oxidative stress, abnormal mRNA degradation, endocytosis, vesicle transport, and cell cycle regulation. These results contribute to a better understanding of the function and mechanism of Tsf in ticks. Furthermore, this study provides a novel antigen for anti-tick vaccine from the perspective of inhibiting tick iron metabolism.","PeriodicalId":11728,"journal":{"name":"Entomologia Generalis","volume":null,"pages":null},"PeriodicalIF":5.6000,"publicationDate":"2023-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transferrin affects food intake and reproduction in the hard tick Haemaphysalis longicornis\",\"authors\":\"Duo Wang, Hongxia Li, Xiaojing Zhang, Xuanxuan Wang, Xiaohan Di, Zhijun Yu, Fang Wang, Yankai Zhang, Jingze Liu\",\"doi\":\"10.1127/entomologia/2023/2065\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Transferrin (Tsf) is an extracellular protein with a high affinity for iron in vertebrates, but its function and mechanism in ticks are poorly understood. This study investigated Tsf in the hard tick Haemaphysalis longicornis Neumann (Ixodida: Ixodidae) for the first time. The results showed that Tsf was expressed in three developmental stages (larva, nymph, and female) and in various tissues (salivary glands, ovary, midgut, and Malpighian tubules), with higher expression levels observed after a blood meal. Using the Escherichia coli expression system, it was revealed that the hard tick Tsf protein exhibited iron chelation, radical-scavenging, antibacterial, and hemolytic activities in vitro. Silencing Tsf using RNA interference (RNAi) had adverse effects on the feeding ability and reproduction of H. longicornis, resulting in decreased engorgement weight, ovary weight, egg mass weight, egg hatching rate as well as a prolonged incubation period of eggs from oviposition to larvae hatching. Additionally, proteomics was used to investigate the mechanisms underlying the effects of Tsf on food intake and reproduction in H. longicornis females. The results revealed that Tsf may affect these processes through various pathways, including the ubiquitin–proteasome pathway, lipid metabolic pathways, carbohydrate metabolic pathways, oxidative stress, abnormal mRNA degradation, endocytosis, vesicle transport, and cell cycle regulation. These results contribute to a better understanding of the function and mechanism of Tsf in ticks. 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Transferrin affects food intake and reproduction in the hard tick Haemaphysalis longicornis
Transferrin (Tsf) is an extracellular protein with a high affinity for iron in vertebrates, but its function and mechanism in ticks are poorly understood. This study investigated Tsf in the hard tick Haemaphysalis longicornis Neumann (Ixodida: Ixodidae) for the first time. The results showed that Tsf was expressed in three developmental stages (larva, nymph, and female) and in various tissues (salivary glands, ovary, midgut, and Malpighian tubules), with higher expression levels observed after a blood meal. Using the Escherichia coli expression system, it was revealed that the hard tick Tsf protein exhibited iron chelation, radical-scavenging, antibacterial, and hemolytic activities in vitro. Silencing Tsf using RNA interference (RNAi) had adverse effects on the feeding ability and reproduction of H. longicornis, resulting in decreased engorgement weight, ovary weight, egg mass weight, egg hatching rate as well as a prolonged incubation period of eggs from oviposition to larvae hatching. Additionally, proteomics was used to investigate the mechanisms underlying the effects of Tsf on food intake and reproduction in H. longicornis females. The results revealed that Tsf may affect these processes through various pathways, including the ubiquitin–proteasome pathway, lipid metabolic pathways, carbohydrate metabolic pathways, oxidative stress, abnormal mRNA degradation, endocytosis, vesicle transport, and cell cycle regulation. These results contribute to a better understanding of the function and mechanism of Tsf in ticks. Furthermore, this study provides a novel antigen for anti-tick vaccine from the perspective of inhibiting tick iron metabolism.
期刊介绍:
Its scope covers all aspects of basic and applied research dealing with insects and more broadly with arthropods inhabiting wild, agricultural and/or urban habitats. The journal also considers research integrating various disciplines and issues within the broad field of entomology and ecology.
Entomologia Generalis publishes high quality research articles on advances in knowledge on the ecology and biology of arthropods, as well as on their importance for key ecosystems services, e.g. as biological control and pollination. The journal devotes special attention to contributions providing significant advances (i) on the fundamental knowledge and on sustainable control strategies of arthropod pests (including of stored products) and vectors of diseases, (ii) on the biology and ecology of beneficial arthropods, (iii) on the spread and impact of invasive pests, and (iv) on potential side effects of pest management methods.
Entomologia Generalis welcomes review articles on significant developments in the field of entomology. These are usually invited by the editorial board, but proposals may be sent to the Editor-in-Chief for preliminary assessment by the editorial board before formal submission to the journal. The journal also considers comments on papers published in Entomologia Generalis, as well as short notes on topics that are of broader interest.