Role of ZFP36L1 in suppressing human coronavirus replication
Presenter(s)
Andrew Villasenor, Tooba Shafeeque Ahmed Momin, Malabika Bhowmik
Files
Description
ZFP36L1 is a CCCH-type zinc figure protein (ZFP) where zinc ions coordinate the protein structure in a tetrahedral geometry by binding to cystine-cystine or cysteine-histidine amino acids. ZFP36L1’s unique structure enables it to interact with a wide variety of molecules including RNA; thus, it could modulate several cellular processes including virus replication. Several CCCH-type ZFPs have shown their antiviral efficacy against various DNA and RNA viruses. However, the role of ZFP36L1 in the human coronavirus is little explored. We used human coronavirus (HCoV)-OC43 to determine the role of ZFP36L1 on its replication. We overexpressed and knockdown ZFP36L1 in HCT-8 cells individually using lentivirus transduction. Wild type, ZFP36L1 overexpressed, and ZFP36L1 knockdown cells were each infected with HCoV-OC43, and the virus titer in each cell line was measured over 96 hours post-infection (p.i.). Our results show that HCoV-OC43 replication was significantly reduced with ZFP36L1 overexpression while ZFP36L1 knockdown significantly enhanced virus replication. ZFP36L1 knockdown HCT-8 cells started producing infectious virus at 48 hours p.i. which was an earlier timepoint as compared to wild-type and ZFP36L1 overexpressed cells. Wild-type and ZFP36L1 overexpressed HCT-8 cells started producing infectious virus at 72 hours p.i. Overall, the current study showed that overexpression of ZFP36L1 suppressed human coronavirus (OC43) production
Publication Date
4-19-2023
Project Designation
Graduate Research
Primary Advisor
Mrigendra Rajput, Amit Singh
Primary Advisor's Department
Biology
Keywords
Stander Symposium, College of Arts and Sciences
Institutional Learning Goals
Scholarship
Recommended Citation
"Role of ZFP36L1 in suppressing human coronavirus replication" (2023). Stander Symposium Projects. 3185.
https://ecommons.udayton.edu/stander_posters/3185
Comments
Presentation: 11:40 a.m.-12:00 p.m., Science Center 150