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Basic Characteristics of Mutations
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Mutation Site
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N146D |
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Mutation Site Sentence
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Thirty of 85 vaccine-immunized failure child patients had at least one amino acid substitutions in a determinant region, including T126A(7), T126S(1), I126T(5), P127T(2), Q129R(1), Q129H(1), T131N(1), M133L(3), M133T(1), F134L(1), T140I(1), T143M(2), D144A(2), G145R(4), and N146D(1). |
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Mutation Level
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Amino acid level |
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Mutation Type
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Nonsynonymous substitution |
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Gene/Protein/Region
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S |
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Standardized Encoding Gene
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S
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Genotype/Subtype
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- |
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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 Virus Infection
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Immune
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Y |
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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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- |
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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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29629487
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Title
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Quasispecies characters of hepatitis B virus in immunoprophylaxis failure infants
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Author
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Wang X,Deng W,Qian K,Deng H,Huang Y,Tu Z,Huang A,Long Q
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Journal
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European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology
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Journal Info
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2018 Jun;37(6):1153-1162
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Abstract
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Hepatitis B vaccination prevents 80-95% of transmission and reduces the incidence of HBV in children. The variations in the a determinant of HBV surface antigen (HBsAg) have been reported to be the most prevalent cause for vaccine or antibody escape. There is a conflicting evidence on as to whether escape mutants arise de novo in infected infants or whether the mutants, that have preexisted maternally, subsequently undergo selective replication in the infant under immune pressure. Here, we report that nearly 65% (55 of 85) vaccination failure in child patients has no amino acid substitution in a determinant as seen by Sanger sequencing. We further employed an Illumina sequencing platform-based method to detect HBV quasispecies in four immunoprophylaxis failure infants and their mothers. In our data, the substitution rate of amino acid located at a determinant is relatively low (< 10%), I/T126A, C124S, F134Y, K141Q, Q129H, D144A, G145V, and N146K, which showed no statistical difference to their mothers, proving that these vaccine escape mutants preexist maternally as minor variants. Besides that, bioinformatical analysis showed that the binding affinity of high variation epitopes (amino acid divergence in mother and their infants > 20%) to related HLA molecules was generally decreased, these traces of immune escape suggesting that immune pressure was present and was effective in all samples.
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Sequence Data
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SRR1916064;SRR1916065;SRR1916067;SRR1916066;SRR1916068;SRR1916069;SRR1916070;SRR1916071
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