Researcher ORCID Identifier
0009-0005-9997-815X
Graduation Year
2023
Document Type
Open Access Senior Thesis
Degree Name
Bachelor of Arts
Department
Biochemistry
Reader 1
Bethany Caulkins
Reader 2
Erin Jones
Terms of Use & License Information
Rights Information
© 2023 Carissa V Napier
Abstract
Feline coronavirus (FCoV) infection is ubiquitous in domestic cats, and up to 12% of FCoV-infected cats may succumb to Feline Infectious Peritonitis (FIP). FIP is a highly lethal infectious disease caused by FIP virus (FIPV), the virulent biotype of FCoV. It is difficult to properly diagnose FIP, and to this date, there is no effective FCoV vaccine nor licensed therapeutic for FIPV. Considering the threat FIP poses to feline health, there is a demand from both owners and veterinarians for a proper therapeutic to effectively treat the infection. 5-aminolevulinic acid (5-ALA) is a highly bioavailable amino acid that is naturally synthesized in animal cells and has shown significant antiviral activity against coronaviruses SARS-CoV-2 and FIPV. The inhibition of FIPV infection is most likely due to the intracellular accumulation of a downstream metabolite called protoporphyrin IX (PPIX) from 5-ALA supplementation, which can bind to G-quadruplex (G4) structures in the viral genome and therefore inhibit viral translation and replication processes. This propositional study is designed to investigate the potential stabilization of G4s in FIPV by PPIX and its subsequent inhibition of the viral life cycle both in vitro and in feline cells.
Recommended Citation
Napier, Carissa V., "Potential Mechanism of 5-ALA treatment against Feline Infectious Peritonitis Virus Infection by Downstream Metabolite PPIX" (2023). Scripps Senior Theses. 2214.
https://scholarship.claremont.edu/scripps_theses/2214