The recent publication of representative genomic sequences of GBV-C ha
s permitted the selection of PCR primers for detection of GBV-C in cli
nical samples by PCR techniques. Traditional amplification methodologi
es which couple reverse transcription polymerase chain reaction (RT-PC
R) and Southern blot detection are slow, cumbersome, and can be techni
que dependent. This has hampered studies to determine the clinical sig
nificance of GBV-C. We report the selection of highly conserved PCR pr
imers and a probe useful for semi-automated RT-PCR using the Abbott LC
x(R) system. This adaptation of the LCx(R) system expands its capabili
ties to include the detection of RNA by RT-PCR, in addition to DNA det
ection by ligase chain reaction (LCR). (C) 1998 Elsevier Science B.V.
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