雷帕霉素靶点(TOR)是白纹伊蚊血液消化和繁殖所必需的

IF 4.1 1区 农林科学 Q1 ENTOMOLOGY
Chen Zhang, Jiayan Shen, Ruoyun Lan, Jiaying Xu, Tingting Ma, Bin Tang, Shigui Wang
{"title":"雷帕霉素靶点(TOR)是白纹伊蚊血液消化和繁殖所必需的","authors":"Chen Zhang, Jiayan Shen, Ruoyun Lan, Jiaying Xu, Tingting Ma, Bin Tang, Shigui Wang","doi":"10.1007/s10340-024-01862-2","DOIUrl":null,"url":null,"abstract":"<p><i>Aedes albopictus</i> transmits the virus through repeated blood feeding behavior and can also vertically transmit the virus to its offspring. In this study, we analyzed the expression of the <i>TOR</i> gene in <i>Ae. albopictus</i> and found that it was highest in female mosquitoes 24 h after feeding, particularly in the head and thorax. Then, we used to feed method to silence the <i>TOR</i> gene of female mosquitoes and make them suck blood. Silencing <i>TOR</i> resulted in downregulation of amino acid transporter genes <i>SLC7A5</i> and <i>SLC3A2</i>, as well as regulatory intermediates <i>Rheb</i> and <i>Frizzled-2</i> in other signaling pathways. In terms of midgut blood digestion, silencing <i>TOR</i> led to reduced glucose metabolism while affecting trypsin (TRY) and chymotrypsin (CHY) enzymes involved in midgut blood digestion, thereby delaying the process. Regarding reproduction, silencing <i>TOR</i> resulted in decreased expression levels of <i>Vitellogenin 2 </i>(<i>Vg2</i>) and <i>Vg3</i> gene, leading to reduced Vg content in the ovary. Additionally, downstream protein synthesis-related genes <i>4E-binding protein</i> (<i>4E-BP</i>) and <i>S6 kinase</i> (<i>S6K</i>) within the TOR pathway were affected. Although there were no significant changes observed in egg number or diameter, ovarian development cycle delay occurred along with signs of desiccation and shrinkage in some eggs. Moreover, both egg weight and hatching rate showed a significant decrease. The experimental results suggest that <i>TOR</i> regulates the blood digestion and reproduction process of <i>A. albopictus</i> by influencing post-vampire protease activity and protein synthesis, such as Vg. This provides a theoretical foundation for developing cost-effective and large-scale prevention and control measures for <i>A. albopictus</i>.</p>","PeriodicalId":16736,"journal":{"name":"Journal of Pest Science","volume":"26 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Target of rapamycin (TOR) is necessary for the blood digestion and reproduction of Aedes albopictus\",\"authors\":\"Chen Zhang, Jiayan Shen, Ruoyun Lan, Jiaying Xu, Tingting Ma, Bin Tang, Shigui Wang\",\"doi\":\"10.1007/s10340-024-01862-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><i>Aedes albopictus</i> transmits the virus through repeated blood feeding behavior and can also vertically transmit the virus to its offspring. In this study, we analyzed the expression of the <i>TOR</i> gene in <i>Ae. albopictus</i> and found that it was highest in female mosquitoes 24 h after feeding, particularly in the head and thorax. Then, we used to feed method to silence the <i>TOR</i> gene of female mosquitoes and make them suck blood. Silencing <i>TOR</i> resulted in downregulation of amino acid transporter genes <i>SLC7A5</i> and <i>SLC3A2</i>, as well as regulatory intermediates <i>Rheb</i> and <i>Frizzled-2</i> in other signaling pathways. In terms of midgut blood digestion, silencing <i>TOR</i> led to reduced glucose metabolism while affecting trypsin (TRY) and chymotrypsin (CHY) enzymes involved in midgut blood digestion, thereby delaying the process. Regarding reproduction, silencing <i>TOR</i> resulted in decreased expression levels of <i>Vitellogenin 2 </i>(<i>Vg2</i>) and <i>Vg3</i> gene, leading to reduced Vg content in the ovary. Additionally, downstream protein synthesis-related genes <i>4E-binding protein</i> (<i>4E-BP</i>) and <i>S6 kinase</i> (<i>S6K</i>) within the TOR pathway were affected. Although there were no significant changes observed in egg number or diameter, ovarian development cycle delay occurred along with signs of desiccation and shrinkage in some eggs. Moreover, both egg weight and hatching rate showed a significant decrease. The experimental results suggest that <i>TOR</i> regulates the blood digestion and reproduction process of <i>A. albopictus</i> by influencing post-vampire protease activity and protein synthesis, such as Vg. This provides a theoretical foundation for developing cost-effective and large-scale prevention and control measures for <i>A. albopictus</i>.</p>\",\"PeriodicalId\":16736,\"journal\":{\"name\":\"Journal of Pest Science\",\"volume\":\"26 1\",\"pages\":\"\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-02-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pest Science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1007/s10340-024-01862-2\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENTOMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pest Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1007/s10340-024-01862-2","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

摘要

白纹伊蚊通过反复吸血传播病毒,也可垂直传播给后代。在这项研究中,我们分析了TOR基因在伊蚊中的表达。结果发现,雌蚊摄食24 h后白纹伊蚊感染率最高,尤其是头部和胸部。然后用喂食法沉默雌蚊TOR基因,使其吸血。沉默TOR导致氨基酸转运基因SLC7A5和SLC3A2,以及调节中间体Rheb和frizzed -2在其他信号通路中的下调。在中肠血液消化方面,沉默TOR导致葡萄糖代谢降低,同时影响参与中肠血液消化的胰蛋白酶(TRY)和凝乳胰蛋白酶(CHY)酶,从而延缓这一过程。在生殖方面,沉默TOR导致卵黄原蛋白2 (Vg2)和Vg3基因表达水平降低,导致卵巢内Vg含量降低。此外,TOR通路内下游蛋白合成相关基因4e结合蛋白(4E-BP)和S6激酶(S6K)也受到影响。虽然没有观察到卵子数量或直径的显著变化,但卵巢发育周期延迟,一些卵子出现干燥和收缩的迹象。卵重和孵化率均显著降低。实验结果表明,TOR通过影响吸血后白纹伊蚊的蛋白酶活性和蛋白质合成来调节白纹伊蚊的血液消化和繁殖过程。这为制定具有成本效益的大规模白纹伊蚊防控措施提供了理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Target of rapamycin (TOR) is necessary for the blood digestion and reproduction of Aedes albopictus

Aedes albopictus transmits the virus through repeated blood feeding behavior and can also vertically transmit the virus to its offspring. In this study, we analyzed the expression of the TOR gene in Ae. albopictus and found that it was highest in female mosquitoes 24 h after feeding, particularly in the head and thorax. Then, we used to feed method to silence the TOR gene of female mosquitoes and make them suck blood. Silencing TOR resulted in downregulation of amino acid transporter genes SLC7A5 and SLC3A2, as well as regulatory intermediates Rheb and Frizzled-2 in other signaling pathways. In terms of midgut blood digestion, silencing TOR led to reduced glucose metabolism while affecting trypsin (TRY) and chymotrypsin (CHY) enzymes involved in midgut blood digestion, thereby delaying the process. Regarding reproduction, silencing TOR resulted in decreased expression levels of Vitellogenin 2 (Vg2) and Vg3 gene, leading to reduced Vg content in the ovary. Additionally, downstream protein synthesis-related genes 4E-binding protein (4E-BP) and S6 kinase (S6K) within the TOR pathway were affected. Although there were no significant changes observed in egg number or diameter, ovarian development cycle delay occurred along with signs of desiccation and shrinkage in some eggs. Moreover, both egg weight and hatching rate showed a significant decrease. The experimental results suggest that TOR regulates the blood digestion and reproduction process of A. albopictus by influencing post-vampire protease activity and protein synthesis, such as Vg. This provides a theoretical foundation for developing cost-effective and large-scale prevention and control measures for A. albopictus.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Pest Science
Journal of Pest Science 生物-昆虫学
CiteScore
10.40
自引率
8.30%
发文量
114
审稿时长
6-12 weeks
期刊介绍: Journal of Pest Science publishes high-quality papers on all aspects of pest science in agriculture, horticulture (including viticulture), forestry, urban pests, and stored products research, including health and safety issues. Journal of Pest Science reports on advances in control of pests and animal vectors of diseases, the biology, ethology and ecology of pests and their antagonists, and the use of other beneficial organisms in pest control. The journal covers all noxious or damaging groups of animals, including arthropods, nematodes, molluscs, and vertebrates. Journal of Pest Science devotes special attention to emerging and innovative pest control strategies, including the side effects of such approaches on non-target organisms, for example natural enemies and pollinators, and the implementation of these strategies in integrated pest management. Journal of Pest Science also publishes papers on the management of agro- and forest ecosystems where this is relevant to pest control. Papers on important methodological developments relevant for pest control will be considered as well.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信