We constructed a recombinant feline herpesvirus type 1 (FHV-1) which was deleted in a defined region (450 bp) within the thymidine kinase (TK) gene (C7301 dlTK) [Yokoyama et al. (1995) J Vet Med Sci 57: 709-714]. In this report, we carried out two experiments to assess the pathogenicity and vaccine efficacy of the recombinant C7301J/TK in cats. The first experiment showed that, following multiple inoculation of the recombinant C730WITK by intraocular, intranasal and oral routes, the virus was sufficiently attenuated in cats, although a high titer of the virus was recovered from target organs (eye, nose, and mouth). In the second experiment, two intramuscular vaccinations with the recombinant C7301dlTK protected cats to a significant degree against subsequent challenge with the parent FHV-1 strain C7301 at 4 weeks after the last vaccination. These results demonstrate that the recombinant C730WITK is effective as a live attenuated vaccine with a clear genetic marker. © Springer-Verlag 1996.
CITATION STYLE
Yokoyama, N., Maeda, K., Tohya, Y., Kawaguchi, Y., Shin, Y. S., Ono, M., … Mikami, T. (1996). Pathogenicity and vaccine efficacy of a thymidine kinase-deficient mutant of feline herpesvirus type 1 in cats. Archives of Virology, 141(3–4), 481–494. https://doi.org/10.1007/BF01718312
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