Chakraborty, D.; Sannigrahi, A.; Kaif, M.; Patra, A.; Thakkar, D.; Roy, R.

Dengue virus, and other viral pathogens such as SARS-CoV-2 and Zika, utilize specialized glycoproteins to facilitate the fusion of its lipid membrane with that of the host cell, a critical step for viral entry and infection. This membrane fusion process is significantly influenced by factors such as host cell membrane lipid composition, membrane architecture, and cell surface receptors. However, the specific mechanisms by which dengue virus membrane fusion is modulated by the cell membrane lipids are not fully elucidated. We investigate the role of oxidised cholesterol metabolite, 25-hydroxycholesterol (25-HC) in inhibiting dengue virus infection using virus fusion and viral infection assays. We demonstrate that 25-HC significantly impedes the membrane fusion capability of the dengue virus, thereby inhibiting viral entry and infection in cell cultures. Apart from inhibiting membrane fusion, pre-exposure to 25-HC upregulates CH25H which inhibits virus growth. Indeed, CH25H gene is upregulated along with other ISGs in various cell types as a defence response to dengue virus infection. These insights into the modulation of dengue virus membrane fusion by lipid cofactors in the host cell membrane present a promising avenue for the development of strategies aimed at inhibiting viral membrane fusion, thereby potentially curtailing the spread of the infection. For example, we show that other inhibitors that target mechanisms distinct from 25-HC action on membrane fusion display strong positive synergy in virus inhibition with 25-HC.