Jam. Calder et al., MONITORING BABESIA-BOVIS INFECTIONS IN CATTLE BY USING PCR-BASED TESTS, Journal of clinical microbiology, 34(11), 1996, pp. 2748-2755
The sensitivity and specificity of PCR tests based on the small-subuni
t rRNA gene sequence of Babesia bovis were compared in a blind study o
f experimentally infected cattle with the corresponding parameters of
the complement fixation (CF) test currently used in the United States
to screen for bovine babesiosis. Cattle were experimentally infected w
ith a single inoculum of a cloned laboratory strain of B. bovis. Blood
samples were collected and tested over a period covering from the day
of infection to 10 months postinfection, The level of parasitemia (pe
rcent infected erythrocytes) present in each sample was estimated from
test results and was plotted as a function of time postinfection. The
se data are the first describing the course of infection by methods ca
pable of detecting parasitemias in the range of 10(-7)%, which frequen
tly occur in the carrier state, Parasitemias in the samples tested str
ongly influenced the sensitivity and negative predictive value of the
PCR-based tests which varied with time postinfection, The average sens
itivities of the three PCR-based tests for B. bovis ranged from 58 to
70% for a single determination, while the sensitivity of the CF test w
as only 6%. Both PCR-based and CF tests for B. bovis had high specific
ity values ranging from 96 to 100%.