The molecular toll pathway repertoire in anopheline mosquitoes.

IF 2.7 3区 农林科学 Q1 FISHERIES Developmental and comparative immunology Pub Date : 2024-11-08 DOI:10.1016/j.dci.2024.105287
Victoria L Rhodes, Robert M Waterhouse, Kristin Michel
{"title":"The molecular toll pathway repertoire in anopheline mosquitoes.","authors":"Victoria L Rhodes, Robert M Waterhouse, Kristin Michel","doi":"10.1016/j.dci.2024.105287","DOIUrl":null,"url":null,"abstract":"<p><p>Innate immunity in mosquitoes has received much attention due to its potential impact on vector competence for vector-borne disease pathogens, including malaria parasites. The nuclear factor (NF)-κB-dependent Toll pathway is a major regulator of innate immunity in insects. In mosquitoes, this pathway controls transcription of the majority of the known canonical humoral immune effectors, mediates anti-bacterial, anti-fungal and anti-viral immune responses, and contributes to malaria parasite killing. However, besides initial gene annotation of putative Toll pathway members and genetic analysis of the contribution of few key components to immunity, the molecular make-up and function of the Toll pathway in mosquitoes is largely unexplored. To facilitate functional analyses of the Toll pathway in mosquitoes, we report here manually annotated and refined gene models of Toll-like receptors and all putative components of the intracellular signal transduction cascade across 19 anopheline genomes, and in two culicine genomes. In addition, based on phylogenetic analyses, we identified differing levels of evolutionary constraint across the intracellular Toll pathway members, and identified a recent radiation of TOLL1/5 within the Anopheles gambiae complex. Together, this study provides insight into the evolution of TLRs and the putative members of the intracellular signal transduction cascade within the genus Anopheles.</p>","PeriodicalId":11228,"journal":{"name":"Developmental and comparative immunology","volume":null,"pages":null},"PeriodicalIF":2.7000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental and comparative immunology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.dci.2024.105287","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0

Abstract

Innate immunity in mosquitoes has received much attention due to its potential impact on vector competence for vector-borne disease pathogens, including malaria parasites. The nuclear factor (NF)-κB-dependent Toll pathway is a major regulator of innate immunity in insects. In mosquitoes, this pathway controls transcription of the majority of the known canonical humoral immune effectors, mediates anti-bacterial, anti-fungal and anti-viral immune responses, and contributes to malaria parasite killing. However, besides initial gene annotation of putative Toll pathway members and genetic analysis of the contribution of few key components to immunity, the molecular make-up and function of the Toll pathway in mosquitoes is largely unexplored. To facilitate functional analyses of the Toll pathway in mosquitoes, we report here manually annotated and refined gene models of Toll-like receptors and all putative components of the intracellular signal transduction cascade across 19 anopheline genomes, and in two culicine genomes. In addition, based on phylogenetic analyses, we identified differing levels of evolutionary constraint across the intracellular Toll pathway members, and identified a recent radiation of TOLL1/5 within the Anopheles gambiae complex. Together, this study provides insight into the evolution of TLRs and the putative members of the intracellular signal transduction cascade within the genus Anopheles.

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
疟蚊的分子收费途径汇集。
蚊子的先天免疫因其对包括疟原虫在内的病媒传播疾病病原体的潜在影响而备受关注。核因子(NF)-κB 依赖性 Toll 通路是昆虫先天免疫的主要调节器。在蚊子体内,这一途径控制着大多数已知的典型体液免疫效应因子的转录,介导抗细菌、抗真菌和抗病毒免疫反应,并有助于杀死疟原虫。然而,除了对推测的 Toll 通路成员进行初步基因注释和对少数关键成分对免疫的贡献进行遗传分析外,蚊子中 Toll 通路的分子组成和功能在很大程度上尚未得到探索。为了便于对蚊子的 Toll 通路进行功能分析,我们在此报告了经人工标注和完善的 Toll 样受体基因模型,以及细胞内信号转导级联的所有假定成分,涉及 19 个疟蚊基因组和两个高丽疟蚊基因组。此外,基于系统发育分析,我们发现了细胞内 Toll 通路成员之间不同程度的进化限制,并在冈比亚按蚊复合体中发现了 TOLL1/5 的最新辐射。总之,这项研究为TLRs和细胞内信号转导级联的推定成员在冈比亚按蚊属中的进化提供了深入的见解。
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
CiteScore
6.20
自引率
6.90%
发文量
206
审稿时长
49 days
期刊介绍: Developmental and Comparative Immunology (DCI) is an international journal that publishes articles describing original research in all areas of immunology, including comparative aspects of immunity and the evolution and development of the immune system. Manuscripts describing studies of immune systems in both vertebrates and invertebrates are welcome. All levels of immunological investigations are appropriate: organismal, cellular, biochemical and molecular genetics, extending to such fields as aging of the immune system, interaction between the immune and neuroendocrine system and intestinal immunity.
期刊最新文献
A recombinant sPLA2 protein promotes gut mucosal barrier against bacterial infection in fish. Functional characterization of peroxiredoxin 5 from yellowtail clownfish (Amphiprion clarkii): Immunological expression assessment, antioxidant activities, heavy metal detoxification, and nitrosative stress mitigation. Zebrafish use conserved CLR and TLR signaling pathways to respond to fungal PAMPs in zymosan. The molecular toll pathway repertoire in anopheline mosquitoes. Dietary supplementation with pseudostellaria heterophylla polysaccharide enhanced immunity and changed mRNA expression of spleen in chicks
×
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