Journal Articles

Permanent URI for this collectionhttps://mro.massey.ac.nz/handle/10179/7915

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    Efficacy of oral remdesivir in treating feline infectious peritonitis: a prospective observational study of 29 cats
    (SAGE Publications on behalf of the International Cat Care Veterinary Society and Feline Veterinary Medical Association, 2025-05-27) Renner KA; Cattin R; Kimble B; Munday J; White A; Coggins S
    Objectives: The primary aim of this prospective observational study was to document clinical progression, survival, remission and relapse in New Zealand cats with feline infectious peritonitis (FIP) that were treated with compounded oral remdesivir with or without initial parenteral remdesivir therapy. The secondary aims were to determine the optimal monitoring protocols and report the adverse effects of treatment and complications associated with FIP. Methods: A total of 29 client-owned cats with a clinical diagnosis of FIP were prospectively recruited. Cats were administered oral remdesivir (30 mg/kg q24h), rounded up to the nearest capsule size as the sole treatment, or after initial parenteral remdesivir (15–30 mg/kg q24h). Rechecks were recommended at weeks 1, 2, 4, 8 and 12 during treatment, and at 2 and 12 weeks after treatment. A full physical examination (including neurological and ophthalmic examination) and point-of-care ultrasound were performed at each recheck. A complete blood count and biochemistry panel were performed at weeks 4, 8, 12 and 24. Molnupiravir was offered as a rescue therapy for cats that relapsed. Results: In total, 25 (86%) cats entered remission and survived beyond 6 months (range 6–27). A total of 22 (75%) cats achieved remission within 84 days while receiving oral remdesivir. Three cats received subsequent molnupiravir rescue therapy to achieve remission. Five cats (20%) experienced relapse: four with non-effusive disease and one with effusive disease. Notably, 4/8 (50%) non-effusive cases relapsed, compared with only 1/20 (5%) with effusive disease. Conclusions and relevance: This study demonstrates that oral remdesivir at a dose rate of 30 mg/kg q24h is an effective treatment for effusive FIP. The survival rate in non-effusive cats was significantly lower; therefore, an increased dose rate or frequency of administration should be considered in these cats. Oral remdesivir is a viable antiviral option where GS-441524 is unavailable.
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    In Vitro Effects of Doxycycline on Replication of Feline Coronavirus
    (MDPI AG, 7/03/2021) Ghosh S; Dunowska M
    Feline infectious peritonitis (FIP) is a sporadic fatal disease of cats caused by a virulent variant of feline coronavirus (FCoV), referred to as FIP virus (FIPV). Treatment options are limited, and most of the affected cats die or are euthanized. Anecdotally, doxycycline has been used to treat FIP-affected cats, but there are currently no data to support or discourage such treatment. The aim of this study was to establish whether doxycycline inhibits replication of FIPV in vitro. The virus was cultured in Crandell-Rees feline kidney cells with various concentrations of doxycycline (0 to 50 µg/mL). The level of FIPV in cultures was determined by virus titration and FCoV-specific reverse-transcription quantitative PCR. Cell viability was also monitored. There was no difference in the level of infectious virus or viral RNA between doxycycline-treated and untreated cultures at 3, 12- and 18-hours post-infection. However, at 24 h, the growth of FIPV was inhibited by approximately two logs in cultures with >10 µg/mL doxycycline. This inhibition was dose-dependent, with inhibitory concentration 50% (IC50) 4.1 µg/mL and IC90 5.4 µg/mL. Our data suggest that doxycycline has some inhibitory effect on FIPV replication in vitro, which supports future clinical trials of its use for the treatment of FIP-affected cats.