Fiscus S A, Rivoire B L, Teramoto Y A
Syngene Products and Research, Fort Collins, CO 80524.
Adv Exp Med Biol. 1987;218:559-68. doi: 10.1007/978-1-4684-1280-2_71.
Isolates of feline infectious peritonitis virus (FIPV) vary in their degree of virulence and have antigenically and functionally different peplomer glycoproteins. We tested the most virulent isolate, FIPV-79-1146 and the avirulent isolate, FIPV-UCD-2 in vivo in order to better understand the pathogenesis of FIP. Specific pathogen free cats were inoculated with either FIPV-79-1146 or FIPV-UCD-2. After 28 days cats which had received FIPV-79-1146 were either dead or showing clinical signs of FIP. The FIPV-UCD-2 inoculated cats seroconverted but remained healthy and were then divided into three groups. One group was not manipulated, one group received a second dose of FIPV-UCD-2, and the third group received FIPV-79-1146. One month later all FIPV-UCD-2 cats which had subsequently received FIPV-79-1146 were dead of FIP while the FIPV-UCD-2 inoculated cats remained healthy. Antibody mediated immune enhancement of FIP disease was not observed. Serum neutralization assays demonstrated that only those cats which received FIPV-79-1146 developed neutralizing antibodies to FIPV-79-1146. However, all cats except uninoculated controls developed neutralizing titers to FIPV-UCD-2. Competition ELISAs were used to analyze the specific humoral immune responses of cats to structural polypeptides of the viruses.