Literature DB >> 8462361

Concentrating missense mutations in core gene of hepatitis B virus. Evidence for adaptive mutation in chronic hepatitis B virus infection.

W L Chuang1, M Omata, T Ehata, O Yokosuka, M Ohto.   

Abstract

To elucidate the temporal relationship between liver damage and mutation(s) in hepatitis B virus core gene, serial sera from a progressive liver disease patient and an asymptomatic carrier were studied. By direct sequencing, missense mutations in the core gene were only found in serum from the progressive liver disease patient during the period with frequent exacerbation. Using methods of cloning and sequencing, missense mutations were also found in clones derived from the progressive liver disease patient at a relatively early phase, but strains with a missense mutation from earlier sera did not exist in sera of a later period. Furthermore, there was a tendency of concentrating missense mutations in clones derived from the progressive liver disease patient. These data suggested that missense mutations in the core gene that occurred at an earlier phase might evoke an immune response to eliminate mutated virus and that concentrating missense mutations during a phase of exacerbation might be a result of adaptive mutation.

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Year:  1993        PMID: 8462361     DOI: 10.1007/bf01316786

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


  29 in total

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Journal:  Nature       Date:  1990-11-15       Impact factor: 49.962

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Journal:  Nature       Date:  1990-11-15       Impact factor: 49.962

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Journal:  Tissue Antigens       Date:  1987-11

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Authors:  H C Thomas; M Jacyna; J Waters; J Main
Journal:  Semin Liver Dis       Date:  1988-11       Impact factor: 6.115

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Authors:  B G Hall
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

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Journal:  Gastroenterology       Date:  1985-11       Impact factor: 22.682

9.  A common antiviral cytotoxic T-lymphocyte epitope for diverse major histocompatibility complex haplotypes: implications for vaccination.

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Journal:  Proc Natl Acad Sci U S A       Date:  1992-04-01       Impact factor: 11.205

10.  Defective presentation to class I-restricted cytotoxic T lymphocytes in vaccinia-infected cells is overcome by enhanced degradation of antigen.

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Journal:  J Exp Med       Date:  1988-10-01       Impact factor: 14.307

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4.  Coexistence of two distinct secretion mutations (P5T and I97L) in hepatitis B virus core produces a wild-type pattern of secretion.

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Authors:  Zhi-Tao Yang; Su-Yuan Huang; Li Chen; Feng Liu; Xiao-Hui Cai; Yang-Fan Guo; Ming-Jie Wang; Yue Han; De-Min Yu; Jie-Hong Jiang; Dong-Hua Zhang; Qi-Ming Gong; Guo-Qing Zhang; Guo-Qing Zang; Zhong-Hua Lu; Li-Hua Huang; Xin-Xin Zhang
Journal:  J Clin Microbiol       Date:  2015-04-29       Impact factor: 5.948

Review 6.  Host immune response and variations in the virus genome: pathogenesis of liver damage caused by hepatitis B virus.

Authors:  N V Naoumov; A L Eddleston
Journal:  Gut       Date:  1994-08       Impact factor: 23.059

7.  Reduced secretion of virions and hepatitis B virus (HBV) surface antigen of a naturally occurring HBV variant correlates with the accumulation of the small S envelope protein in the endoplasmic reticulum and Golgi apparatus.

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Journal:  J Virol       Date:  2005-11       Impact factor: 5.103

8.  Variations in the core region of hepatitis C virus genomes in patients with chronic hepatitis.

Authors:  M Kurosaki; N Enomoto; F Marumo; C Sato
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

9.  Persistence of Hepatitis B Virus DNA and the Tempos between Virion Secretion and Genome Maturation in a Mouse Model.

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Review 10.  Virion Secretion of Hepatitis B Virus Naturally Occurring Core Antigen Variants.

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  10 in total

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