Transferrin affects food intake and reproduction in the hard tick Haemaphysalis longicornis

IF 5.6 1区 农林科学 Q1 ENTOMOLOGY Entomologia Generalis Pub Date : 2023-12-11 DOI:10.1127/entomologia/2023/2065
Duo Wang, Hongxia Li, Xiaojing Zhang, Xuanxuan Wang, Xiaohan Di, Zhijun Yu, Fang Wang, Yankai Zhang, Jingze Liu
{"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. 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":"24 1","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2023-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Entomologia Generalis","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1127/entomologia/2023/2065","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0

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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
转铁蛋白影响长角血蜱的食物摄取和繁殖
转铁蛋白(Tsf)是一种在脊椎动物中对铁具有高亲和力的细胞外蛋白,但其在蜱中的功能和机制尚不清楚。本研究首次对硬蜱长角血蜱(伊蚊目:伊蚊科)中的Tsf进行了研究。结果表明,Tsf在幼虫、若虫和雌虫的3个发育阶段和不同组织(唾液腺、卵巢、中肠和马尔比氏小管)中均有表达,血餐后表达量较高。利用大肠杆菌表达系统,发现硬蜱Tsf蛋白在体外具有铁螯合、自由基清除、抗菌和溶血活性。RNA干扰(RNA interference, RNAi)对长角天竺蜂的取食能力和繁殖能力产生不利影响,导致长角天竺蜂的膨体重、卵巢重、卵质量重、卵孵化率下降,卵从产卵到幼虫孵化期延长。此外,我们还利用蛋白质组学研究了Tsf对长角家蝇雌性摄食和繁殖的影响机制。结果表明,Tsf可能通过多种途径影响这些过程,包括泛素-蛋白酶体途径、脂质代谢途径、碳水化合物代谢途径、氧化应激、异常mRNA降解、内吞作用、囊泡运输和细胞周期调节。这些结果有助于更好地理解Tsf在蜱中的作用和机制。此外,本研究还从抑制蜱铁代谢的角度为抗蜱疫苗提供了一种新的抗原。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Entomologia Generalis
Entomologia Generalis 生物-昆虫学
CiteScore
7.10
自引率
18.80%
发文量
72
审稿时长
>12 weeks
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.
期刊最新文献
Sublethal and transgenerational effects of chlorfenapyr on physiological and developmental traits of Spodoptera frugiperda Unraveling the feeding response and intergenerational sublethal effects of flonicamid on Rhopalosiphum padi A novel potential nAChR variation and the upregulation of CYP304A1 contribute to resistance against lambda-cyhalothrin and spinosad in Bactrocera dorsalis Ultraviolet and violet light enhance the attraction efficacy of semiochemicals for the Asian longhorned beetle Compensating from a bad start in life: linking male energy reserves to reproductive output in a polyphagous moth
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1