登革热
谱系(遗传)
病毒学
登革热病毒
生物
病毒
灵敏度(控制系统)
遗传学
进化生物学
基因
电子工程
工程类
作者
Hawa Sophia Bouzidi,S. SEN,Géraldine Piorkowski,Laura Pezzı,Nazlı Ayhan,Albin Fontaine,Thomas Canivez,Manon Geulen,Rayane Amaral,Gilda Grard,C. Durand,Xavier de Lamballerie,Franck Touret,Raphaëlle Klitting
标识
DOI:10.1038/s41467-024-52819-z
摘要
Abstract Dengue fever is the most important arbovirosis for public health, with more than 5 million cases worldwide in 2023. Mosnodenvir is the first anti-dengue compound with very high preclinical pan-serotype activity, currently undergoing phase 2 clinical evaluation. Here, by analyzing dengue virus (DENV) genomes from the 2023-2024 epidemic in the French Caribbean Islands, we show that they all exhibit mutation NS4B:V91A, previously associated with a marked decrease in sensitivity to mosnodenvir in vitro. Using antiviral activity tests on four clinical and reverse-genetic strains, we confirm a marked decrease in mosnodenvir sensitivity for DENV-2 ( > 1000 fold). Finally, combining phylogenetic analysis and experimental testing for resistance, we find that virus lineages with low sensitivity to mosnodenvir due to the V91A mutation likely emerged multiple times over the last 30 years in DENV-2 and DENV-3. These results call for increased genomic surveillance, in particular to track lineages with resistance mutations. These efforts should allow to better assess the activity profile of DENV treatments in development against circulating strains.
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