慢性乙肝病毒感染患者2年内乙型肝炎病毒的演变

Hepatitis research and treatment Pub Date : 2011-01-01 Epub Date: 2011-07-12 DOI:10.1155/2011/939148
Tao Shen, Xin-Min Yan, Jin-Ping Zhang, Jin-Li Wang, Rong-Xia Zuo, Li Li, Lin-Pin Wang
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引用次数: 7

摘要

从慢性HBV感染患者获得的全长HBV分离株的突变在三个时间点进行评估:1天,6个月和31个月。5个核苷酸变异和一个18 bp的preS1缺失至少在前两年保持不变,发生在HBsAg亲水性区的C339T突变和导致聚合酶V560A取代的T770C是在第3个时间点的测序克隆中发现的新的点突变。编码区的内部缺失在第3个时间点明显出现。除了报道的供体和受体外,剪接子还包括两个新的5'剪接供体和三个新的3'剪接受体,并可能产生推定的hbv剪接蛋白或截断的preS蛋白。ALT、HBeAg和病毒DNA载量在随访期间发生变化。这些数据证明了hbv感染患者在进化过程中基因组的多样性。结合临床资料,在该患者中发现的HBV变异可能有助于病毒持续感染或肝脏发病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Evolution of Hepatitis B Virus in a Chronic HBV-Infected Patient over 2 Years.

Mutations in full-length HBV isolates obtained from a chronic HBV-infected patient were evaluated at three time points: 1 day, 6 months, and 31 months. While 5 nucleotides variation, and an 18 bp deletion of preS1 have been kept in during at least the first two years, C339T mutation occurring in the hydrophilic region of HBsAg and T770C that caused polymerase V560A substitution were the new point mutations found existing in sequenced clones of the 3rd time point. Internal deletion of coding region obviously appeared in the 3rd time point. The splicers included two new 5'-splice donors and three new 3'-splice acceptors besides the reported donors and acceptors and may have produced presumptive HBV-spliced proteins or truncated preS proteins. ALT, HBeAg and viral DNA load varied during the follow-up years. These data demonstrated the diversity of genomes in HBV-infected patient during evolution. Combined with clinical data, the HBV variants discovered in this patient may contribute to viral persistence of infection or liver pathogenesis.

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