Rodriguez-Frias F, Buti M, Jardi R, Cotrina M, Viladomiu L, Esteban R, Guardia J
Liver Unit, Hospital General Universitario Valle Hebron, Barcelona, Spain.
Hepatology. 1995 Dec;22(6):1641-7. doi: 10.1002/hep.1840220605.
The precore-core gene of hepatitis B virus (HBV) was directly sequenced from serum samples of 42 patients with chronic B hepatitis (19 hepatitis B e antigen [HBeAg]+ and 23 anti-HBE+). Viral genotypes were determined by comparison with 11 reference sequences and by restriction analysis. Genotype A was identified in 16 cases, genotype D in 24 cases, and other genotypes in 2 cases. Precore mutations, mainly M1 (stop at codon 28), were differently distributed among the viral genotypes: 3 cases (18.8%) with genotype A and 18 cases (75%) with genotype D. In sequences with precore mutants, the encapsidation signal was more stable (negative stabilization energy) than in sequences without precore mutants. In genotype A, the M1 mutation coexisted with a second mutation (C-->T at position 1858 in codon 15), and both mutations were paired in the secondary structure of the RNA encapsidation signal, which justified the rare presence of precore mutants in this genotype. The analysis showed different distribution of mutations depending on the viral genotype; patients with genotype D were more likely to have persistent HBV infection by selection of precore mutants. Multiple amino acid substitutions were detected in the core region, mainly in two subsequences that have been previously described as epitopes (flanked by codons 11 to 27 and 74 to 83); the presence of these mutations was significantly related to the presence of precore variants which abolished the expression of HBeAg.(ABSTRACT TRUNCATED AT 250 WORDS)
对42例慢性乙型肝炎患者(19例乙肝e抗原[HBeAg]阳性和23例抗-HBe阳性)的血清样本进行了乙肝病毒(HBV)前核心-核心基因的直接测序。通过与11条参考序列比较及限制性分析确定病毒基因型。16例鉴定为A基因型,24例为D基因型,2例为其他基因型。前核心突变主要为M1(密码子28处的终止突变),在不同病毒基因型中的分布不同:A基因型中有3例(18.8%),D基因型中有18例(75%)。在前核心突变体序列中,包装信号比无前核心突变体的序列更稳定(负稳定能)。在A基因型中,M1突变与第二个突变(密码子15处第1858位C→T)共存,且这两个突变在RNA包装信号的二级结构中配对,这解释了该基因型中前核心突变体罕见的原因。分析表明,突变的分布因病毒基因型而异;D基因型患者通过选择前核心突变体更易发生持续性HBV感染。在核心区域检测到多个氨基酸替换,主要在两个先前被描述为表位的子序列中(密码子11至27和74至83两侧);这些突变的存在与消除HBeAg表达的前核心变体的存在显著相关。(摘要截短于250词)