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Published on: September 7, 2017
Antiviral studies of feline infectious peritonitis virus in vitro
1Department of Medicine, School of Veterinary Medicine, University of California, Davis 95616.
Abstract:
Sixteen compounds were tested for their ability to inhibit the replication in vitro of feline infectious peritonitis virus (FIPV), a coronavirus that causes a lethal, immunologically mediated illness in domestic and exotic cats. Six of the compounds, when incubated with cells and titrations of the virus, were found to reduce the virus titres by 0.401 to 0.833 log10 (P < 0.05), using the cytopathic effect as endpoint. Further inhibition studies were performed to determine the 50 per cent effective dose (ED50) levels for these six compounds. Selectivity indices (50 per cent cytotoxic dose [CD50]/ED50) provided the following order of antiviral activity: pyrazofuin > 6-azauridine > 3-deazaguanosine > hygromycin B > fusidic acid > dipyridamole. Compounds which had no statistically significant effect on FIPV in the same assay were caffeic acid, carbodine, 3-deazauridine, 5-fluoroorotic acid, 5-fluorouracil, D(+)glucosamine, indomethacin, D-penicillamine, rhodamine and taurine.
Insights
Six compounds inhibited feline infectious peritonitis virus (FIPV) replication in vitro. Pyrazofurin showed the highest antiviral activity, offering potential for new FIPV treatments in cats.
Area of Science:
- Veterinary Virology
- Antiviral Drug Discovery
- Feline Infectious Diseases
Background:
- Feline infectious peritonitis virus (FIPV) causes a lethal, immune-mediated disease in cats.
- Effective antiviral treatments for FIPV are limited.
- In vitro studies are crucial for identifying potential FIPV inhibitors.
Purpose of the Study:
- To screen compounds for in vitro antiviral activity against FIPV.
- To determine the efficacy and selectivity of identified FIPV inhibitors.
- To establish an order of antiviral potency for promising compounds.
Main Methods:
- In vitro screening of sixteen compounds against FIPV replication.
- Quantification of viral inhibition using cytopathic effect endpoint.
- Determination of 50% effective dose (ED50) and 50% cytotoxic dose (CD50).
- Calculation of selectivity indices (CD50/ED50) to rank antiviral activity.
Main Results:
- Six out of sixteen tested compounds demonstrated significant inhibition of FIPV replication (P < 0.05).
- Antiviral activity was observed with reduction in virus titres ranging from 0.401 to 0.833 log10.
- Pyrazofurin exhibited the highest antiviral activity, followed by 6-azauridine, 3-deazaguanosine, hygromycin B, fusidic acid, and dipyridamole.
Conclusions:
- Several compounds show promise as potential antiviral agents against FIPV in vitro.
- Pyrazofurin demonstrates superior antiviral potency among the tested compounds.
- Further research is warranted to explore the therapeutic potential of these compounds for feline infectious peritonitis.
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