Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4361491 | Cell Host & Microbe | 2010 | 11 Pages |
SummaryAutophagy influences numerous cellular processes, including innate and adaptive immunity against intracellular pathogens. However, some viruses, including dengue virus (DENV), usurp autophagy to enhance their replication. The mechanism for a positive role of autophagy in DENV infection is unclear. We present data that DENV induction of autophagy regulates cellular lipid metabolism. DENV infection leads to an autophagy-dependent processing of lipid droplets and triglycerides to release free fatty acids. This results in an increase in cellular β-oxidation, which generates ATP. These processes are required for efficient DENV replication. Importantly, exogenous fatty acids can supplant the requirement of autophagy in DENV replication. These results define a role for autophagy in DENV infection and provide a mechanism by which viruses can alter cellular lipid metabolism to promote their replication.
► DENV-induced autophagosomes partially colocalize with lipid droplets ► DENV-induced autophagy depletes lipid droplets and triglycerides ► Autophagy increases cellular β-oxidation, which is required for DENV replication ► Exogenous fatty acids supplant the requirement of autophagy for DENV replication