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Journal of Clinical Microbiology, 03 1997, 673-675, Vol 35, No. 3
DA Gamble, A Lobbiani, M Gramegna, LE Moore and G Colucci
A diagnostic test for feline infectious peritonitis virus (FIPV) infection
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 target 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 tested 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 positive, while 1 was negative. Ten of
the 11 cats ill from other causes tested negative, while 1 was positive. On
the basis of clinical laboratory and histopathologic criteria, the
preliminary sensitivity and specificity of the assay were 91.6 and 94%,
respectively.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Development of a nested PCR assay for detection of feline infectious peritonitis virus in clinical specimens
Animal Medical Center, New York, New York, USA.
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