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Basic Characteristics of Mutations
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Mutation Site
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T473C |
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Mutation Site Sentence
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Five of these six mutations may be mainly divided into two types: (1) C3116T and C705T mutations, which were detected in all clones isolated from group C, but emerged with lower proportions in groups M and N; and (2) C3175T, C96T and T473C mutations, which were detected in clones isolated from one mother (M4) in group M and four infected neonates (N2, 3, 7 and 8) in group N, but not in clones isolated from mothers in group C. |
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Mutation Level
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Nucleotide level |
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Mutation Type
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Synonymous substitution |
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Gene/Protein/Region
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PreS;S |
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Standardized Encoding Gene
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S
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Genotype/Subtype
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C |
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Viral Reference
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M12906
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Functional Impact and Mechanisms
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Disease
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Hepatitis B Virus Infection
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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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Y |
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Treatment
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- |
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Location
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- |
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Literature Information
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PMID
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19272629
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Title
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Association between genomic heterogeneity of hepatitis B virus and intrauterine infection
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Author
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Cheng H,Su H,Wang S,Shao Z,Men K,Li M,Li S,Zhang J,Xu J,Zhang H,Yan Y,Xu D
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Journal
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Virology
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Journal Info
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2009 Apr 25;387(1):168-75
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Abstract
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Hepatitis B virus (HBV) intrauterine infection remains to be an important cause for a large number of persistent hepatitis B surface antigen (HBsAg) positive carriers in areas with a high HBV prevalence, particularly in China and Southeast Asia. In this study, the possible association between the HBV genomic heterogeneity and intrauterine infection was investigated by comparing the quasi species isolated from eight pairs of HBsAg-positive mothers and their neonates, who were infected intrauterinely with HBV, with clones from eight HBsAg-positive mothers whose neonates were not infected with HBV. The proportion of clones with specific mutations was compared among different subject groups, and phylogenetic analysis was performed to evaluate the significance of specific mutations. It was observed that the core promoter with conserved major functional regions and conserved hepatitis B e antigen (HBeAg) might be beneficial to HBV maternal-fetal transmission. Particularly, A1762T/G1764A mutations seemed to be disadvantageous for fetal infection. It was also shown that amino acid substitutions located in the immune epitopes of HBsAg were strongly associated with intrauterine HBV transmission. The clones with mutations such as amino acid P110S in preS1 region, P36L in preS2 region and C107R in S region might infect fetuses more readily. In addition, positively selected site analysis confirmed the above results.
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Sequence Data
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-
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