Mason Archival Repository Service

Efficacy of Host-Kinase Inhibitors as Antiviral Agents Against Venezuelan Equine Encephalitis Virus

Show simple item record

dc.contributor.advisor Narayanan, Aarthi
dc.contributor.author Lark, Tyler
dc.creator Lark, Tyler
dc.date 2017-12-06
dc.date.accessioned 2018-05-17T17:15:40Z
dc.date.available 2018-05-17T17:15:40Z
dc.identifier doi:10.13021/G88T24
dc.identifier.uri https://hdl.handle.net/1920/10954
dc.description.abstract Venezuelan equine encephalitis virus (VEEV) is a New World alphavirus that is naturally transmitted through mosquito vectors resulting in human infections. This virus is classified as a category B pathogen and a select agent as it is highly infectious and retains infectivity when transmitted as an aerosol. There is currently no therapeutic or vaccine candidate that is available to the civilian population for the treatment of VEEV exposures. With the ability of viruses to develop resistance to antiviral strategies that target viral components, it will be of strategic value to target specific host proteins to inhibit the viral life-cycle. Such host-based therapeutic candidates are also likely to find broad spectrum applicability in the treatment of infections by of other viral pathogens in addition to VEEV that employ the same host-based candidates. We show that inhibition of host kinases, AP2-associated protein kinase 1 (AAK1) and cyclin G-associated kinase (GAK), associated with clathrin-mediated endocytosis and intracellular trafficking results in a decrease of VEEV load in infected cells. siRNA knockdown of AAK and GAK yielded a decrease in viral titers along with alteration of viral protein levels. The small molecules azaindole and erlotinib (FDA approved) were found to have strong antiviral properties. Both drugs affected the ability of the virion to traffic effectively through the cell, preventing the movement from the plasma membrane and potentially, the ER network. Time of addition experiments showed that the drugs exhibit therapeutic potential, as both worked against established infections. These results show the effectiveness of AAK and GAK inhibitors in inhibiting VEEV infection. Ongoing research is exploring the mechanisms involved in this inhibitory process.
dc.language.iso en en_US
dc.subject AAK 1 en_US
dc.subject GAK en_US
dc.subject clathrin en_US
dc.subject AP2 en_US
dc.subject AP1 en_US
dc.subject VEEV en_US
dc.title Efficacy of Host-Kinase Inhibitors as Antiviral Agents Against Venezuelan Equine Encephalitis Virus en_US
dc.type Thesis en_US
thesis.degree.name Master of Science in Biology en_US
thesis.degree.level Master's en_US
thesis.degree.discipline Biology en_US
thesis.degree.grantor George Mason University en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search MARS


Advanced Search

Browse

My Account

Statistics