Summary |
A reverse transcription polymerase chain reaction ( RT-PCR ) assay was developed for the detection of bovine ephemeral fever virus ( BEFV ). Two primer sets, BEFV-Pl I BEFV-P2 and BEFV-P3 / BEFV-P4, were used for the RT-PCR. Two DNA fragment, 824 bp and of 255 bp, could be specifically amplified respectively. Both Taiwan isolates and Japan isolate of BEFV could be detected positively. The sensitivity ofRT-PCR with primers BEFV-Pl I BEFV-P2 for the detection of BEFV was 104 TCID50 The sensitivity increased 104-fold when a pair of nested primers BEFV-P3 / BEFV-P4 was used. Twenty-one out of 31 ( 67.74 % ) samples, suspected of BEF infection, were diagnosed positive by this method, and two isolates of BEFV were isolated in this epidemic occurrence.
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