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Basic Characteristics of Mutations
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Mutation Site
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2447_489del |
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Mutation Site Sentence
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Performing alignment showed that over the 2-year period, deletions across overlapping region of polymerase/preS1 (g.2447_489del 1256) or preS1/preS2 (g.3018_3202del 183, and g.3144_56del 126), and pre-S1 initiation codon mutations (g.2846_2865del 18) with or without internal deletions mutations (g.3024_3193del 168) were prevalent (22/26, in 85% of the clones) (Figure 2). |
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Mutation Level
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Nucleotide level |
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Mutation Type
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Deletion |
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Gene/Protein/Region
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P;PreS1 |
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Standardized Encoding Gene
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P
S
|
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Genotype/Subtype
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C |
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Viral Reference
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-
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Functional Impact and Mechanisms
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Disease
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Hepatitis B, Chronic
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Immune
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- |
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Target Gene
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-
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Clinical and Epidemiological Correlations
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Clinical Information
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- |
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Treatment
|
- |
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Location
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China |
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Literature Information
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PMID
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21785721
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Title
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Evolution of Hepatitis B Virus in a Chronic HBV-Infected Patient over 2 Years
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Author
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Shen T,Yan XM,Zhang JP,Wang JL,Zuo RX,Li L,Wang LP
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Journal
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Hepatitis research and treatment
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Journal Info
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2011;2011:939148
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Abstract
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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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Sequence Data
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DQ377159-377165;EU306713-306714;EU306722-306729;EU439005;EU439008-439014;EU439025
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