HETEROGENEITY OF HEPATITIS-B VIRUS C-GENE SEQUENCES - IMPLICATIONS FOR AMPLIFICATION AND SEQUENCING

被引:21
作者
MISKA, S
GUNTHER, S
VASSILEV, M
MEISEL, H
PAPE, G
WILL, H
机构
[1] MAX PLANCK INST BIOCHEM, W-8033 MARTINSRIED, GERMANY
[2] HUMBOLDT UNIV BERLIN, INST VIROL, O-1086 BERLIN, GERMANY
[3] UNIV MUNICH, INST IMMUNOL, W-8000 MUNICH 2, GERMANY
关键词
HBV MUTANTS; POLYMERASE CHAIN REACTION; HBV CHRONIC CARRIERS; LIVER DISEASE; INTERFERON TREATMENT; PRECORE PROTEIN;
D O I
10.1016/S0168-8278(05)80009-1
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Occasionally direct sequencing of amplified hepatitis B virus DNA leads to weak signals on autoradiograms. Using amplified C-gene sequences we investigated whether this is due to sequence heterogeneity of virus populations and use of inappropriate primers for direct sequencing. High C-gene sequence heterogeneity (point mutations, stop codons and a one codon deletion) was observed in HBV genomes from serum of a chronic carrier who underwent interferon treatment. The type of C-gene mutations detected by direct sequencing depended on the type of primers used. Cloning and sequencing of amplified C-gene sequences demonstrated that this was due to mutations in the region complementary to the sequencing primer. These data demonstrate the existence of novel HBV C-gene mutants and imply that multiple or degenerate sequencing and amplification primers are essential for accurate evaluation of the extent of HBV C-gene heterogeneity. Based on comparative sequence analysis of all available completely or incompletely sequenced C-genes, guidelines for optimal primer design are proposed for similar studies.
引用
收藏
页码:53 / 61
页数:9
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