Da. Gamble et al., DEVELOPMENT OF A NESTED PCR ASSAY FOR DETECTION OF FELINE INFECTIOUS PERITONITIS VIRUS IN CLINICAL SPECIMENS, Journal of clinical microbiology, 35(3), 1997, pp. 673-675
A diagnostic test for feline infectious peritonitis virus (FIPV) infec
tion based on a nested PCR (nPCR) assay was developed and tested with
FIPV, feline enteric coronavirus (FECV), canine coronavirus (CCV), and
transmissible gastroenteritis virus (TGEV) and clinical fluid samples
from cats with effusive feline infectious peritonitis (FIP). The targ
et sequence for the assay is in the S1 region of the peplomer protein
E2 gene, A vaccine strain of FIPV and two wild-type FIPV strains teste
d positive, but FECV, TGEV, and CCV tested negative, Preliminary tests
with 12 cats with clinical evidence of effusive FIP and 11 cats with
an illness associated with effusions, but attributed to other causes,
were performed. Eleven of the 12 cats with effusive FIP tested positiv
e, while 1 was negative, Ten of the 11 cats ill from other causes test
ed negative, while 1 was positive. On the basis of clinical laboratory
and histopathologic criteria, the preliminary sensitivity and specifi
city of the assay were 91.6 and 94%, respectively.