Universal Primers for Detection and Sequencing of Hepatitis B Virus

Hepatitis B virus (HBV) has been divided into 10 genotypes, A to J, based on an 8 % nucleotide sequence divergence be-tween genotypes. The conventional practice of using a single set of primers to amplify a near-complete HBV genome is hampered by its low analytical sensitivity. The current practice of using overlapping conserved primer sets to amplify a complete HBV genome in a clinical sample is limited by the lack of pan-primers to detect all HBV genotypes. In this study, we designed six highly conserved, overlapping primer sets to cover the complete HBV genome. We based our design on the sequences of 5,154 HBV genomes of genotypes A to I downloaded from the GenBank nucleotide database. These primer sets were tested on 126 plasma samples from Malaysia, containing genotypes A to D and with viral loads ranging from 20 to>79,780,000 IU/ml. The overall success rates for PCR amplification and sequencing were>96 % and>94%, respectively. Similarly, there was 100 % amplification and sequencing success when the primer sets were tested on an HBV reference panel of genotypes A to G. Thus, we have established primer sets that gave a high analytical sensitivity for PCR-based de-tection of HBV and a high rate of sequencing success for HBV genomes in most of the viral genotypes, if not all, without prior known sequence data for the particular genotype/genome. Hepatitis B virus (HBV) has a partially double-stranded-DNA, 3.2-kb-long genome. The virus replicates through the error-prone reverse transcription of an RNA intermediate (1), leading to a high degree of viral genetic variation. HBV, like RNA viruses, has a high evolutionary rate, 104 to 105 substi