Ml. Jackson et al., FELINE LEUKEMIA-VIRUS DETECTION BY ELISA AND PCR IN PERIPHERAL-BLOOD FROM 68 CATS WITH HIGH, MODERATE, OR LOW SUSPICION OF HAVING FELV-RELATED DISEASE, Journal of veterinary diagnostic investigation, 8(1), 1996, pp. 25-30
Clinicopathologic criteria were used to group 68 cats according to hig
h, moderate, or low suspicion of having feline leukemia virus (FeLV)-r
elated disease. Peripheral blood samples were tested for FeLV antigen
by enzyme-linked immunosorbent assay (ELISA) and for FeLV DNA by polym
erase chain reaction (PCR). There was no significant difference betwee
n ELISA and PCR results in the 68 cats. In the high-suspicion group, 4
6% (11/24) of cytopenic cats were test positive (ELISA and PCR) and 87
% (13/15) with hemopoietic neoplasms were test-positive. Also within t
he high suspicion group, test-positive cats were 2.5 times more likely
to die within the 1 year follow-up period than were test-negative (EL
ISA and PCR) cats. Among cats in the moderate-suspicion group, 15% (2/
13) were test-positive, and none (0/16) of the cats in the low suspici
on group was test positive. The relative risk of a positive test (ELIS
A and PCR) in the high suspicion group was 3.7 times that for the mode
rate-suspicion group and 22.8 times that for the low suspicion group.
There was no significant difference in the relative risk of a positive
test result between the moderate and low suspicion groups. The result
s indicate that FeLV detection by PCR can be adapted for diagnostic pu
rposes using peripheral blood samples, however, results do not differ
significantly from FeLV ELISA results. Also, a proportion of cats with
a high suspicion of having FeLV-related cytopenia and hemopoietic tum
ors are negative for both circulating FeLV antigen and DNA. These cats
may not have FeLV-related disease, or FeLV may exist in a disease-pro
ducing but nonreplicating form ultimately detectable by PCR in tissues
other than peripheral blood.