摘要
Flaviviruses pose growing global health threats and are transmitted by Aedes mosquitoes. Yet, how these viruses overcome early mosquito immunity remains unclear. Here, we reveal a cross-host immune evasion strategy in which the flavivirus NS1 protein, abundantly secreted into infected human serum, is taken up by mosquitoes during blood feeding and rapidly internalized into midgut epithelial cells—prior to viral replication. NS1 hijacks the mosquito spliceosome-associated factor Prp19 to promote miR-275-5p maturation, which suppresses the caspase gene CASPS19, blocking apoptosis and enabling early viral replication. Engineered mosquitoes expressing a miR-275 sponge show enhanced resistance to dengue and Zika viruses. These findings uncover a mechanism by which a viral protein presented in infected host blood reprograms vector gene regulation, establishing a paradigm of cross-species immune manipulation by flaviviruses.
| 源语言 | 英语 |
|---|---|
| 期刊论文编号 | 6535 |
| 期刊 | Nature Communications |
| 卷 | 17 |
| 期 | 1 |
| DOI | |
| 出版状态 | 已出版 - 12月 2026 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 3 良好健康与福祉
学术指纹
探究 'Host serum-circulating flavivirus NS1 co-opts mosquito miRNA processing to suppress early immune defense' 的科研主题。它们共同构成独一无二的学术指纹。引用此
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