Komatsu Haruki, Fujisawa Tomoo, Sogo Tsuyoshi, Isozaki Atsushi, Inui Ayano, Sekine Isao, Kobata Makoto, Ogawa Yunosuke
Department of Pediatrics, National Defense Medical College, Saitama, Japan.
J Med Virol. 2002 Jan;66(1):28-33. doi: 10.1002/jmv.2107.
The occurrence of acute hepatitis after failure of immunoprophylaxis in cases of mother-to-infant transmission of hepatitis B virus (HBV) is uncommon. Because immunoprophylaxis failure is caused by the emergence of an "a" determinant escape mutant, the infants usually become HBV carriers. To evaluate whether mutations in the S gene coding for the surface protein that contains the "a" determinant are associated with acute hepatitis after immunoprophylaxis failure, HBV DNA of an infant in with acute hepatitis developed with seroconversion to anti-HBs antibodies at 12 months of age despite administration of anti-hepatitis B immunoglobulin and hepatitis B vaccine was analyzed. The S gene from HBV DNA isolated from the serum of the infant at 12, 19, and 27 months of age was cloned and sequenced. Mutations affecting amino acid residues in the first loop within the "a" determinant (codons 124-147) were found at 12 months of age. Moreover, a novel deletion mutant, with a 1-bp deletion at nucleotide 449 of the S gene, was found at 19 and 27 months of age. This deletion resulted in a frame shift and it introduced a stop codon (TAG) at codon 176. Because the open reading frame of the S gene is completely overlapped by the polymerase gene, mutations in the S gene may affect the polymerase gene. Based on this case, this study suggests that the observed frame-shift mutation in the S gene might affect the polymerase protein and induce prompt suppression of viral replication.
在乙型肝炎病毒(HBV)母婴传播病例中,免疫预防失败后发生急性肝炎的情况并不常见。由于免疫预防失败是由“a”决定簇逃逸突变体的出现引起的,这些婴儿通常会成为HBV携带者。为了评估编码含有“a”决定簇的表面蛋白的S基因中的突变是否与免疫预防失败后的急性肝炎有关,对一名尽管接种了乙型肝炎免疫球蛋白和乙型肝炎疫苗,但在12个月龄时血清转化为抗-HBs抗体并发生急性肝炎的婴儿的HBV DNA进行了分析。对该婴儿12、19和27个月龄时血清中分离出的HBV DNA的S基因进行了克隆和测序。在12个月龄时发现了影响“a”决定簇内第一个环中氨基酸残基(密码子124-147)的突变。此外,在19和27个月龄时发现了一种新的缺失突变体,S基因的核苷酸449处有1个碱基缺失。这种缺失导致了移码,并在密码子176处引入了一个终止密码子(TAG)。由于S基因的开放阅读框与聚合酶基因完全重叠,S基因中的突变可能会影响聚合酶基因。基于该病例,本研究表明,在S基因中观察到的移码突变可能会影响聚合酶蛋白并诱导病毒复制的迅速抑制。