对疾病载体的基因组见解:蚊子、采采蝇、沙蝇和吻虫的不同进化

Lifeng Du , Jingwen Wang
{"title":"对疾病载体的基因组见解:蚊子、采采蝇、沙蝇和吻虫的不同进化","authors":"Lifeng Du ,&nbsp;Jingwen Wang","doi":"10.1016/j.dcit.2025.100053","DOIUrl":null,"url":null,"abstract":"<div><div>Vector-borne diseases pose major global health challenges, with mosquitoes, tsetse flies, and sand flies serving as key insect vectors. This review explores the genomic basis of hematophagy, reproduction, and vector competence across these species. Comparative analyses reveal significant differences in genome size, transposable element content, chemosensory gene repertoires, immune pathways, and symbiotic associations. Mosquitoes possess large, transposable elements (TEs)-rich genomes and expanded antiviral gene families, supporting broad arbovirus transmission. Tsetse flies exhibit compact genomes with viviparous adaptations and obligate symbiosis aiding trypanosome transmission. Sand flies display streamlined genomes with species-specific immune responses and salivary factors that facilitate Leishmania infection. Kissing bugs, with moderate fecundity, lineage-specific immune adaptations, transmit <em>Trypanosoma cruzi</em> across species. These findings highlight how genomic architecture shapes vectorial capacity, offering insights for targeted disease control.</div></div>","PeriodicalId":100358,"journal":{"name":"Decoding Infection and Transmission","volume":"3 ","pages":"Article 100053"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genomic insights into disease vectors: Divergent evolution of mosquitoes, tsetse flies, sand flies and kissing bugs\",\"authors\":\"Lifeng Du ,&nbsp;Jingwen Wang\",\"doi\":\"10.1016/j.dcit.2025.100053\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Vector-borne diseases pose major global health challenges, with mosquitoes, tsetse flies, and sand flies serving as key insect vectors. This review explores the genomic basis of hematophagy, reproduction, and vector competence across these species. Comparative analyses reveal significant differences in genome size, transposable element content, chemosensory gene repertoires, immune pathways, and symbiotic associations. Mosquitoes possess large, transposable elements (TEs)-rich genomes and expanded antiviral gene families, supporting broad arbovirus transmission. Tsetse flies exhibit compact genomes with viviparous adaptations and obligate symbiosis aiding trypanosome transmission. Sand flies display streamlined genomes with species-specific immune responses and salivary factors that facilitate Leishmania infection. Kissing bugs, with moderate fecundity, lineage-specific immune adaptations, transmit <em>Trypanosoma cruzi</em> across species. These findings highlight how genomic architecture shapes vectorial capacity, offering insights for targeted disease control.</div></div>\",\"PeriodicalId\":100358,\"journal\":{\"name\":\"Decoding Infection and Transmission\",\"volume\":\"3 \",\"pages\":\"Article 100053\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Decoding Infection and Transmission\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S294992402500014X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Decoding Infection and Transmission","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S294992402500014X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

病媒传播的疾病构成了重大的全球卫生挑战,蚊子、采采蝇和沙蝇是主要的昆虫媒介。这篇综述探讨了这些物种的噬血、繁殖和媒介能力的基因组基础。比较分析揭示了基因组大小、转座因子含量、化学感觉基因库、免疫途径和共生关联的显著差异。蚊子具有大的、富含转座因子(TEs)的基因组和扩展的抗病毒基因家族,支持广泛的虫媒病毒传播。采采蝇表现出紧凑的基因组,具有胎生适应性和专性共生,有助于锥虫的传播。沙蝇显示具有物种特异性免疫反应的流线型基因组和促进利什曼原虫感染的唾液因子。接吻虫具有中等繁殖力和谱系特异性免疫适应性,可跨物种传播克氏锥虫。这些发现强调了基因组结构如何塑造媒介能力,为有针对性的疾病控制提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genomic insights into disease vectors: Divergent evolution of mosquitoes, tsetse flies, sand flies and kissing bugs

Genomic insights into disease vectors: Divergent evolution of mosquitoes, tsetse flies, sand flies and kissing bugs
Vector-borne diseases pose major global health challenges, with mosquitoes, tsetse flies, and sand flies serving as key insect vectors. This review explores the genomic basis of hematophagy, reproduction, and vector competence across these species. Comparative analyses reveal significant differences in genome size, transposable element content, chemosensory gene repertoires, immune pathways, and symbiotic associations. Mosquitoes possess large, transposable elements (TEs)-rich genomes and expanded antiviral gene families, supporting broad arbovirus transmission. Tsetse flies exhibit compact genomes with viviparous adaptations and obligate symbiosis aiding trypanosome transmission. Sand flies display streamlined genomes with species-specific immune responses and salivary factors that facilitate Leishmania infection. Kissing bugs, with moderate fecundity, lineage-specific immune adaptations, transmit Trypanosoma cruzi across species. These findings highlight how genomic architecture shapes vectorial capacity, offering insights for targeted disease control.
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
自引率
0.00%
发文量
0
×
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