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- W10640494 endingPage "2531" @default.
- W10640494 startingPage "2495" @default.
- W10640494 abstract "Venezuelan equine encephalitis virus (VEEV) is an alphavirus transmitted by mosquitos that can cause a febrile illness and induce severe neurological complications in humans and equine populations. Currently there are no FDA approved vaccines or antiviral treatments to combat VEEV. Proteomic techniques were utilized to create an interactome of the E1 fusion glycoprotein of VEEV. VEEV E1 interacted with a number of cellular chaperone proteins including protein disulfide isomerase family A member 6 (PDIA6). PDI inhibition through LOC14 and/or nitazoxanide treatment effectively decreased production of VEEV and other alphaviruses in vitro, including eastern equine encephalitis virus, Sindbis virus, and chikungunya virus. Decreased oxidoreductive capabilities of PDIs through LOC14 or nitazoxanide treatment impacted both early and late events in viral replication, including the production of non-infectious virions and decreased VEEV E1 disulfide bond formation. Results from this study identified PDIs as critical regulators of alphavirus replication and potential therapeutic targets." @default.
- W10640494 created "2016-06-24" @default.
- W10640494 creator A5004434922 @default.
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- W10640494 creator A5084946612 @default.
- W10640494 date "1974-09-01" @default.
- W10640494 modified "2023-10-18" @default.
- W10640494 title "Lysosomotropic agents" @default.
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