Chao Y C, Tang H S, Hsu C T
Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China.
J Med Virol. 1994 Aug;43(4):397-403. doi: 10.1002/jmv.1890430414.
The complete RNA sequences of hepatitis delta viruses (HDV) isolated at 3 years apart from a chronic delta hepatitis patient in Taiwan were determined. The sequence analysis showed an overall evolution rate of 3.18 x 10(-3) substitutions/nucleotide/year. The evolution rates in different parts of HDV RNA varied. The hypervariable region evolved faster (4.55 x 10(-3) substitutions/nucleotide/year) than the hepatitis delta antigen (HDAg)-coding region (2.60 x 10(-3) substitutions/nucleotide/year) and the autocatalytic region (1.11 x 10(-3) substitutions/nucleotide/year). These data are compatible with the previous finding that the hypervariable region is more divergent than the HDAg-coding region and the autocatalytic regions among the HDV isolates from different geographic areas. No substitution was found in the four previously identified conserved domains of HDV RNA, further confirming their functional importance in viral replication. The evolution rate of this HDV RNA is higher than that determined from the partial RNA sequences of two Japanese HDV isolates and similar to that found in a Lebanon isolate. Further, it was found that this HDV RNA retained the same microheterogeneities at 15 nucleotide positions detected in the RNA 3 years earlier. It is concluded that HDV RNA in patients' serum is extremely heterogeneous, and that the nucleotide substitutions in certain nucleotide positions likely have conferred evolutionary advantages for HDV. Viral sequence evolution is a possible mechanism for chronic HDV infection.
测定了从台湾一名慢性丁型肝炎患者体内相隔3年分离出的丁型肝炎病毒(HDV)的完整RNA序列。序列分析显示总体进化速率为3.18×10⁻³个替换/核苷酸/年。HDV RNA不同部位的进化速率有所不同。高变区进化得更快(4.55×10⁻³个替换/核苷酸/年),快于丁型肝炎抗原(HDAg)编码区(2.60×10⁻³个替换/核苷酸/年)和自身催化区(1.11×10⁻³个替换/核苷酸/年)。这些数据与之前的发现一致,即在来自不同地理区域的HDV分离株中,高变区比HDAg编码区和自身催化区的差异更大。在HDV RNA先前确定的四个保守结构域中未发现替换,进一步证实了它们在病毒复制中的功能重要性。该HDV RNA的进化速率高于从两个日本HDV分离株的部分RNA序列确定的进化速率,与在一个黎巴嫩分离株中发现的进化速率相似。此外,发现该HDV RNA在3年前RNA中检测到的15个核苷酸位置保留了相同的微异质性。得出的结论是,患者血清中的HDV RNA极其异质,并且某些核苷酸位置的核苷酸替换可能赋予了HDV进化优势。病毒序列进化是慢性HDV感染的一种可能机制。