黄病毒
亚基因组mRNA
生物
病毒学
寨卡病毒
核糖核酸
遗传学
病毒
基因
作者
Kristel Doets,Gorben P. Pijlman
摘要
ABSTRACT Live-attenuated flavivirus vaccines confer long-term protection against disease, but the design of attenuated flaviviruses does not follow a general approach. The non-coding, subgenomic flavivirus RNA (sfRNA) is produced by all flaviviruses and is an essential factor in viral pathogenesis and transmission. We argue that modulating sfRNA expression is a promising, universal strategy to finetune flavivirus attenuation for developing effective flavivirus vaccines of the future.
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