Safety and Efficacy of Felid Herpesvirus-1 Deletion Mutants in Cats.
Yao LeeRoger K MaesJohn M KrugerMatti KiupelKim S GiesslerGisela Soboll HusseyPublished in: Viruses (2021)
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.
Keyphrases
- gene expression
- sars cov
- poor prognosis
- binding protein
- dna methylation
- randomized controlled trial
- wild type
- rheumatoid arthritis
- crispr cas
- long non coding rna
- clinical trial
- spinal cord
- single molecule
- chronic rhinosinusitis
- dengue virus
- signaling pathway
- neuropathic pain
- endothelial cells
- high glucose
- study protocol
- genome wide
- disease virus
- stress induced
- circulating tumor cells