| Literature DB >> 33044659 |
Bin Liu1, Ting-Ting Gao1,2, Xiao-Yu Fu1, Zhen-Hao Xu1, Hao Ren1, Ping Zhao1, Zhong-Tian Qi3, Zhao-Ling Qin4.
Abstract
Dengue virus (DENV) is an arthropod-borne viral pathogen and a global health burden. Knowledge of the DENV-host interactions that mediate virus pathogenicity remains limited. Host lipid metabolism is hijacked by DENV for virus replication in which lipid droplets (LDs) play a key role during the virus lifecycle. In this study, we reveal a novel role for phosphatase and tensin homolog deleted on chromosome 10 (PTEN) in LDs-mediated DENV infection. We demonstrate that PTEN expression is downregulated upon DENV infection through post-transcriptional regulation and, in turn, PTEN overexpression enhances DENV replication. PTEN lipid phosphatase activity was found to decrease cellular LDs area and number through Akt/FoxO1/Maf1 signaling, which, together with autophagy, enhanced DENV replication and virus production. We therefore provide mechanistic insight into the interaction between lipid metabolism and the DENV replication cycle.Entities:
Keywords: Akt/FoxO1/Maf1 signaling; Dengue virus; Lipid metabolism; PTEN lipid phosphatase
Year: 2020 PMID: 33044659 DOI: 10.1007/s12250-020-00291-6
Source DB: PubMed Journal: Virol Sin ISSN: 1995-820X Impact factor: 4.327