Abstract

Feline calicivirus (FCV) is a common cat virus causing clinical signs such as oral ulcerations, fever, reduced general condition, pneumonia, limping and occasionally virulent-systemic disease. Efficacious FCV vaccines protect against severe disease but not against infection. FCV is a highly mutagenic RNA virus whose high genetic diversity poses a challenge in vaccine design. The use of only one modified-live FCV strain over several decades might have driven the viral evolution towards more vaccine-resistant variants. The present study investigated the clinical signs, duration, and amount of FCV shedding, RNAemia, haematological changes and acute phase protein reaction in SPF cats after subcutaneous modified-live single strain FCV vaccination or placebo injection and two subsequent oronasal heterologous FCV challenge infections with two different field strains. Neither clinical signs nor FCV shedding from the oropharynx and FCV RNAemia were detected after vaccination. After the first experimental infection, vaccinated cats had significantly lower clinical scores, less increased body temperature and lower acute phase protein levels than control cats. The viral RNA loads from the oropharynx and duration and amount of RNAemia were significantly lower in the vaccinated animals. No clinical signs were observed in any of the cats after the second experimental infection. In conclusion, FCV vaccination was beneficial for protecting cats from severe clinical signs, reducing viral loads and inflammation after FCV challenge.

Highlights

  • Feline calicivirus (FCV) is one of the most common viral pathogens in domestic cats worldwide [1]

  • In a Swiss study, we found significant protection of cats against FCV infection by vaccination; F9 vaccines were mainly used at that time [7]

  • The goals of the present study were: (1) to assess possible shedding of the FCV F9 vaccine virus after initial vaccination and a revaccination; (2) to examine the protective effect of the FCV F9 vaccine towards two recently collected Swiss FCV field strains in two sequential experimental infections; and (3) to investigate the effect of the FCV F9 vaccination on the duration and amount of FCV shedding, RNAemia, haematological changes and the acute phase protein reaction after experimental infections

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Summary

Introduction

Feline calicivirus (FCV) is one of the most common viral pathogens in domestic cats worldwide [1]. In multicat situations such as shelters or breeding catteries, FCV prevalence can range from low to high (10–90%) [2,3,4,5,6,7]. The typical clinical signs of FCV infection are painful oral and lingual ulcerations, gingivitis/stomatitis, fever, inappetence and reduced general condition, with high morbidity and low mortality [1,7,9]. FCV can, in rare cases, lead to virulent systemic disease whereby cats have severe mucosal and/or cutaneous ulcerations and inner organ involvement, and the mortality rates are as high as 60% [10,11,12]

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