Nucleotide sequences of hepatitis GB virus C. Identification of highly conserved domains in the 5′ noncoding region and detection by polymerase chain reaction

Kazuaki Chayama , Jayaram Menon , Katsura Okamoto , Michie Hashimoto , Akihito Tsubota , Masahiro Kobayashi , Yukiko Miyano , Hiromi Koike , Mariko Kobayashi , Isao Koida , Yasuji Arase , Satoshi Saitoh , Yoshiyuki Suzuki , Naoya Murashima , Kenji Ikeda , Hiromitsu Kumada
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引用次数: 10

Abstract

We detected the hepatitis GB virus C genome by reverse transcription-polymerase chain reaction in three Japanese patients with chronic liver diseases. Partial nucleotide sequences of 5′ noncoding, envelope and NS3 regions had 88.6–90.1, 86.388.0, and 78.6–79.6% nucleotide sequence homology compared with the prototype GBV-C genome. However, they showed higher homology with each other (96.197.1, 88.7–91.2, 84.0–87.0%, respectively), suggesting that they were a genotype of GBV-C. The domains that were highly conserved among all these genomes were present in the 5′ noncoding region. The frequency of detecting the genome by the polymerase chain reaction was higher when we used primers designed on these domains compared with primers designed on the core and NS3 region. The virus genome was detected in eight of 50 (16.0%) consecutive Japanese patients with hepatocellular carcinoma who had received more than ten units of blood transfusion, three of 60 (5.0%) patients with non-B, non-C liver disease and 12 of 35 (34.3%) Malaysian patients with non-B chronic liver disease. Since there are no reliable assays to detect hepatitis GB virus C at present, the detection of the genome by the polymerase chain reaction should be useful for diagnosis. Further nucleotide sequence analysis of the genomes is necessary for epidemiological survey studies and vaccine strategy.

乙型肝炎病毒c型的核苷酸序列。5 '非编码区高度保守结构域的鉴定及聚合酶链反应检测
我们用逆转录聚合酶链反应检测了3例日本慢性肝病患者的乙型肝炎病毒C型基因组。5 '非编码区、包膜区和NS3区的部分核苷酸序列与GBV-C原型基因组的同源性分别为88.6-90.1、86.388.0和78.6-79.6%。但同源性较高(分别为96.197.1、88.7-91.2、84.0-87.0%),提示它们属于GBV-C基因型。这些基因组中高度保守的结构域均存在于5′非编码区。在这些区域设计的引物与在核心和NS3区域设计的引物相比,聚合酶链反应检测基因组的频率更高。50例连续接受10个单位以上输血的日本肝细胞癌患者中有8例(16.0%)检测到病毒基因组,60例非b、非c型肝病患者中有3例(5.0%),35例马来西亚非b型慢性肝病患者中有12例(34.3%)检测到病毒基因组。由于目前还没有可靠的检测方法来检测乙型肝炎丙型病毒,因此用聚合酶链反应检测基因组应该有助于诊断。进一步的基因组核苷酸序列分析对于流行病学调查研究和疫苗策略是必要的。
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