Enzyme linked immunosorbent assays (ELISAs) and a nested polymerase chain r
eaction after reverse transcription (RT-PCR) were used for the detection of
the Chinese strain (C strain) of classical swine fever virus (CSFV) in blo
od and tissue samples of experimentally inoculated piglets. One group of 10
piglets was inoculated with C strain material from rabbits and a second on
e with material from infected minipig kidney (MPK) cell culture. Tested blo
od samples were taken on the day of inoculation as well as on days 2, 4, 6,
8, 10, 13 and 16. Samples of spleen, tonsil and brain tissue were collecte
d from piglets on days 6, 8, 10, 13 and 16 and tested for glycoprotein E-RN
S and protein NS2-3 using commercially available ELISA kits. E-RNS and NS2-
3 were detected earlier in blood samples of piglets inoculated with the C s
train propagated in a cell culture. Regardless of propagation the presence
of the viral E-RNS and NS2-3 was detected in spleen and tonsil samples simu
ltaneously. The C strain propagated in a cell culture was found in only one
brain sample, whereas, the virus propagated in rabbits was detected in 70%
of the brain samples. For the detection of the CSFV RNA in blood samples,
a part within the 5' non-coding region was amplified. The differences in th
e results gained by antigen detection in blood samples decreased when neste
d RT-PCR was used. (C) 2001 Elsevier Science B.V. All rights reserved.