Comparison of Six Sets of PCR Primers from Two Different Genomic Regions for Amplification of GB Virus C/Hepatitis G Virus RNA

Abstract

ABSTRACT Forty-four clinical samples positive for GB virus C (GBV-C)/hepatitis G virus (HGV) were tested with six primer sets, four from the 5′ untranslated region (5′-UTR) and two from the NS5a genomic region. Two of the 5′-UTR primer sets, when used in a single-round 60-cycle PCR, detected between 86.4 and 97.7% of the positive samples, while two different sets from the same area, when used in a nested PCR, amplified between 97.7 and 100% of the positive specimens. Both sets from the NS5a region, when used in a single-round PCR, detected 95.5% of the GBV-C/HGV-positive samples. Parallel testing with two PCR sets, one from the 5′-UTR and a second from NS5a, may eliminate false-negative results attributable to the genetic heterogeneity of the virus.