Clinical Follow-Up and Postmortem Findings in a Cat That Was Cured of Feline Infectious Peritonitis with an Oral Antiviral Drug Containing GS-441524

Clinic of Small Animal Medicine, Centre for Clinical Veterinary Medicine, LMU Munich, D-80539 Munich, Germany

Clinical Laboratory, Department of Clinical Diagnostics and Services, Center for Clinical Studies, Vetsuisse Faculty, University of Zurich, CH-8057 Zurich, Switzerland

Division of Paediatric Infectious Diseases, Dr. von Hauner Children’s Hospital, University Hospital, LMU Munich, D-80337 Munich, Germany

Section of Clinical and Comparative Neuropathology, Institute of Veterinary Pathology, Centre for Clinical Veterinary Medicine, LMU Munich, D-80539 Munich, Germany

*Author to whom correspondence should be addressed.

†These authors contributed equally to this work.

Viruses 2022, 14(9), 2040; https://doi.org/10.3390/v14092040

Received: 2 August 2022 / Revised: 31 August 2022 / Accepted: 3 September 2022 / Published: 14 September 2022

1. Introduction

Feline infectious peritonitis (FIP) caused by the feline coronavirus (FCoV) is an infectious disease that occurs in felids worldwide. Infection with wildtype FCoV initially only causes a harmless intestinal infection. Mutation of the virus within the host, however, can lead to the disease FIP, which once clinically apparent is always fatal within a short period of time if left untreated [1]. Hitherto identified mutations mainly result in changes in coronaviral spike proteins, which enable the virus to replicate effectively within macrophages and to spread within the cat [2,3,4]. Subsequent activation of the immune system leads to extensive cytokine release, and thereby exaggerated multisystemic inflammatory lesions. The average survival time without effective treatment is only 8 days after diagnosis [1], and most cats have to be euthanized early due to their severe condition. However, recent studies have demonstrated the efficacy of antiviral compounds containing the nucleoside analog GS-441524 in cats with FIP [5,6,7]. Although successful clinical recovery from FIP has previously been reported [7], this case report is the first description of the complete recovery in a cat whose tissues could be examined after a fatal road traffic accident via necropsy, including histopathology as well as FCoV immunohistochemistry (IHC) and quantitative reverse transcription polymerase chain reaction (RT-qPCR).

In the first controlled study (performed by the same study group) using an oral multicomponent compound called Xraphconn, provided by Mutian Life Sciences Limited, containing GS-441524, 18 cats with naturally occurring and confirmed FIP were treated daily over 84 days [7]. All 18 cats recovered with dramatic resolution of all clinical and laboratory parameters, disappearance of effusion, and complete improvement of neurological signs, if present. Quantitative assessment revealed a large reduction in viral loads (across all measured compartments) within the first few days of treatment. Treatment with Xraphconn containing GS-441524 was highly effective against FIP, without causing clinically relevant adverse effects [7,8].

One cat participating in the abovementioned study [7] died in an unobserved road traffic accident 164 days after the end of treatment. The aim of the present case report was (1) to describe the clinical course during and after treatment, (2) to screen for pathological sequelae of FIP in a cat treated with an oral antiviral drug by examining tissue samples via necropsy and histopathology, and (3) to search for FCoV antigen and viral RNA by IHC and RT-qPCR, respectively.

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