Bläckberg J, Kidd-Ljunggren K
Department of Infectious Diseases, University Hospital, Lund, Sweden.
J Med Virol. 2000 Feb;60(2):107-12. doi: 10.1002/(sici)1096-9071(200002)60:2<107::aid-jmv1>3.0.co;2-t.
Hepatitis B virus (HBV) strains from anti-HBe positive patients often show specific mutations in the precore gene, the core promoter region, or both. The dynamics of seroconversion in relation to the appearance of these mutations has not been studied and compared between defined HBV genotypes. Samples from patients followed during seroconversion from HBeAg to anti-HBe were amplified by polymerase chain reaction (PCR), sequenced and genotyped. Among 16 sets of samples, 6 belonged to genotype A, 6 to genotype D, 2 to genotype B, 1 to genotype C, and 1 to genotype E. Whereas strains from genotypes B, C and E showed changes in the core promoter, precore codon 28 or both, genotype A and D strains displayed a different pattern. In 4 of 6 anti-HBe positive samples from genotype A, the precore had a wild-type sequence while the core promoter sequence showed a specific TGA mutation. In another genotype A strain a precore stop mutation was preceded by a mutation in codon 15, thus conserving base-pairing at the pregenomic RNA level in this region. In contrast, all genotype D strains showed wild-type sequences in both the core promoter and precore codon 28 in pre- and post-seroconversion samples. Thus, in 8 patients with a mean follow-up time of 17 months, wild-type sequences in both the core promoter and precore codon 28 were found after seroconversion to anti-HBe. This study also confirmed, for genotype D, that HBeAg seroconversion often occurs earlier than genomic conversion.
抗HBe阳性患者的乙型肝炎病毒(HBV)毒株通常在precore基因、核心启动子区域或两者中显示出特定突变。尚未对这些突变出现时血清学转换的动态变化进行研究并在明确的HBV基因型之间进行比较。对从HBeAg血清学转换为抗HBe过程中随访的患者样本进行聚合酶链反应(PCR)扩增、测序和基因分型。在16组样本中,6组属于A型基因型,6组属于D型基因型,2组属于B型基因型,1组属于C型基因型,1组属于E型基因型。B、C和E型基因型的毒株在核心启动子、precore密码子28或两者中均有变化,而A型和D型基因型的毒株则呈现不同模式。在6份A型基因型抗HBe阳性样本中的4份中,precore具有野生型序列,而核心启动子序列显示出特定的TGA突变。在另一株A型基因型毒株中,precore终止突变之前密码子15处有一个突变,从而在该区域的前基因组RNA水平上保留了碱基配对。相比之下,所有D型基因型毒株在血清学转换前后的样本中,核心启动子和precore密码子28均显示野生型序列。因此,在平均随访时间为17个月的8例患者中,血清学转换为抗HBe后,在核心启动子和precore密码子28中均发现了野生型序列。本研究还证实,对于D型基因型,HBeAg血清学转换通常比基因组转换更早发生。