Abstract

Felid herpesvirus-1 (FeHV-1) is an important respiratory and ocular pathogen of cats and current vaccines are limited in duration and efficacy because they do not prevent infection, viral nasal shedding and latency. To address these shortcomings, we have constructed FeHV-1 gE-TK- and FeHV-1 PK- deletion mutants (gE-TK- and PK-) using bacterial artificial chromosome (BAC) mutagenesis and shown safety and immunogenicity in vitro. Here, we compare the safety and efficacy of a prime boost FeHV-1 gE-TK- and FeHV-1 PK- vaccination regimen with commercial vaccination in cats. Cats in the vaccination groups were vaccinated at 3-week intervals and all cats were challenge infected 3 weeks after the last vaccination. Evaluations included clinical signs, nasal shedding, virus neutralizing antibodies (VN), cytokine mRNA gene expression, post-mortem histology and detection of latency establishment. Vaccination with gE-TK- and PK- mutants was safe and resulted in significantly reduced clinical disease scores, pathological changes, viral nasal shedding, and viral DNA in the trigeminal ganglia (the site of latency) following infection. Both mutants induced VN antibodies and interferons after immunization. In addition, after challenge infection, we observed a reduction of IL-1β expression, and modulation of TNFα, TGFβ and IL10 expression. In conclusion, this study shows the merits of using FeHV-1 deletion mutants for prevention of FeHV-1 infection in cats.

Highlights

  • Felid herpesvirus-1 (FeHV-1), a member of the alphaherpesvirinae, is an important viral pathogen of cats worldwide

  • Both inactivated and modified live virus (MLV) feline herpesvirus vaccines are widely used in the United States, but protection from FeHV-1 infection is limited in efficacy and shorter in duration compared to feline calicivirus (FCV) and feline panleukopenia virus (FPV), the other two components of feline core vaccination

  • We have previously described the generation of gE, PK, gC- and gE- TK- deletion mutants of FeHV-1 by using bacterial artificial chromosome mutagenesis (BAC) [16,17]

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Summary

Introduction

Felid herpesvirus-1 (FeHV-1), a member of the alphaherpesvirinae, is an important viral pathogen of cats worldwide. Annual revaccination should be carried out in high-risk cats, such as pregnant queens or cats living in multi-cat environments Both inactivated and modified live virus (MLV) feline herpesvirus vaccines are widely used in the United States, but protection from FeHV-1 infection is limited in efficacy and shorter in duration compared to feline calicivirus (FCV) and feline panleukopenia virus (FPV), the other two components of feline core vaccination. Environmental, physiological and chemical stressors can all lead to reactivation from latency and, as such, are associated with renewed replication and shedding of infectious virus [6,7] This implies that clinically normal cats can shed virus and cause disease in unvaccinated animals, explaining the high incidence in shelters

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