DETECTION OF BLUETONGUE VIRUS IN THE BLOOD OF INOCULATED CALVES - COMPARISON OF VIRUS ISOLATION, PCR ASSAY, AND IN-VITRO FEEDING OF CULICOIDES-VARIIPENNIS
Nj. Maclachlan et al., DETECTION OF BLUETONGUE VIRUS IN THE BLOOD OF INOCULATED CALVES - COMPARISON OF VIRUS ISOLATION, PCR ASSAY, AND IN-VITRO FEEDING OF CULICOIDES-VARIIPENNIS, Archives of virology, 136(1-2), 1994, pp. 1-8
The interval after infection when bluetongue virus (BTV) was present i
n the blood of calves inoculated with BTV serotype 10 (BTV 10) was eva
luated by virus isolation (VI) in embryonated chicken eggs (ECE), BTV-
specific polymerase chain reaction (PCR), and in vitro blood feeding o
f vector Culicoides variipennis (C.v.) sonorensis. BTV nucleic acid wa
s detected by PCR in blood cells for 16 to 20 weeks after infection wh
ereas infectious virus was detected by VI in ECE for 2 to 8 weeks. BTV
was detected in calf blood by in vitro feeding of C.v. sonorensis for
only O to 2 weeks after inoculation of calves with BTV 10. Selected b
loods which were positive by PCR analysis but not by VI in ECE were no
t infectious for sheep. The data are consistent with the hypothesis th
at prolonged viremia in BTV-infected cattle results from association o
f the virus with blood cells, especially erythrocytes. The fact that c
alf blood that contained viral nucleic acid as determined by PCR analy
sis, but not infectious virus as determined by VI in ECE, was not infe
ctious for either the insect vector or sheep suggests that cattle whos
e blood contains BTV nucleic acid but not infectious virus are unimpor
tant to the epidemiology of BTV infection.