SREBP-dependent lipidomic reprogramming as a broad-spectrum antiviral target

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Abstract

Viruses are obligate intracellular microbes that exploit the host metabolic machineries to meet their biosynthetic demands, making these host pathways potential therapeutic targets. Here, by exploring a lipid library, we show that AM580, a retinoid derivative and RAR-α agonist, is highly potent in interrupting the life cycle of diverse viruses including Middle East respiratory syndrome coronavirus and influenza A virus. Using click chemistry, the overexpressed sterol regulatory element binding protein (SREBP) is shown to interact with AM580, which accounts for its broad-spectrum antiviral activity. Mechanistic studies pinpoint multiple SREBP proteolytic processes and SREBP-regulated lipid biosynthesis pathways, including the downstream viral protein palmitoylation and double-membrane vesicles formation, that are indispensable for virus replication. Collectively, our study identifies a basic lipogenic transactivation event with broad relevance to human viral infections and represents SREBP as a potential target for the development of broad-spectrum antiviral strategies.

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Yuan, S., Chu, H., Chan, J. F. W., Ye, Z. W., Wen, L., Yan, B., … Yuen, K. Y. (2019). SREBP-dependent lipidomic reprogramming as a broad-spectrum antiviral target. Nature Communications, 10(1). https://doi.org/10.1038/s41467-018-08015-x

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