Literature DB >> 8083662

Evolution of the hepatitis B virus gene during chronic infection in seven patients.

T Uchida1, T T Aye, T Shikata, M Yano, H Yatsuhashi, M Koga, S Mima.   

Abstract

We analyzed the evolution of the precore/core gene of hepatitis B virus (HBV) over a period of 6 to 11 years in seven patients with chronic HBV infection, who exhibited a variety of clinical features. Sequence analysis revealed the following results: (1) HBeAg to anti-HBe seroconversion was correlated roughly with the occurrence of precore-defective mutants, and several years appeared to be required for complete replacement of wild types by mutants; (2) core gene mutations preceded precore-defective mutations and tended to increase with time, although not cumulatively. They occurred not only during serum alanine aminotransferase (ALT) elevations but also after ALT returned to normal; (3) ALT fluctuations appeared to subside with complete replacement of the wild type by the mutant type and/or substantial accumulation of core gene mutations; (4) unexpectedly, the anti-HBe-positive "healthy" carrier was found to harbor the wild type precore gene, as did the HBeAg-positive "healthy" carrier; however, the core gene of the former evolved at a rapid rate; and (5) a partial deletion was recognized in the core gene at the onset of fatal hepatic failure in one patient. Thus, the precore/core mutation was closely related with the clinical features in the patients.

Entities:  

Mesh:

Year:  1994        PMID: 8083662     DOI: 10.1002/jmv.1890430209

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  9 in total

1.  The mechanism of an immature secretion phenotype of a highly frequent naturally occurring missense mutation at codon 97 of human hepatitis B virus core antigen.

Authors:  T T Yuan; G K Sahu; W E Whitehead; R Greenberg; C Shih
Journal:  J Virol       Date:  1999-07       Impact factor: 5.103

2.  A frequent, naturally occurring mutation (P130T) of human hepatitis B virus core antigen is compensatory for immature secretion phenotype of another frequent variant (I97L).

Authors:  T T Yuan; C Shih
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

3.  Subtype-independent immature secretion and subtype-dependent replication deficiency of a highly frequent, naturally occurring mutation of human hepatitis B virus core antigen.

Authors:  T T Yuan; P C Tai; C Shih
Journal:  J Virol       Date:  1999-12       Impact factor: 5.103

4.  Replication advantage and host factor-independent phenotypes attributable to a common naturally occurring capsid mutation (I97L) in human hepatitis B virus.

Authors:  Fat-Moon Suk; Min-Hui Lin; Margaret Newman; Shann Pan; Sheng-Hsuan Chen; Jean-Dean Liu; Chiaho Shih
Journal:  J Virol       Date:  2002-12       Impact factor: 5.103

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

Authors:  Pong Kian Chua; Yu-Mei Wen; Chiaho Shih
Journal:  J Virol       Date:  2003-07       Impact factor: 5.103

6.  Replication of naturally occurring woodchuck hepatitis virus deletion mutants in primary hepatocyte cultures and after transmission to naive woodchucks.

Authors:  M Lu; G Hilken; D Yang; T Kemper; M Roggendorf
Journal:  J Virol       Date:  2001-04       Impact factor: 5.103

7.  Low-level secretion of human hepatitis B virus virions caused by two independent, naturally occurring mutations (P5T and L60V) in the capsid protein.

Authors:  S Le Pogam; T T Yuan; G K Sahu; S Chatterjee; C Shih
Journal:  J Virol       Date:  2000-10       Impact factor: 5.103

8.  Influence of a putative intermolecular interaction between core and the pre-S1 domain of the large envelope protein on hepatitis B virus secretion.

Authors:  Sophie Le Pogam; Chiaho Shih
Journal:  J Virol       Date:  2002-07       Impact factor: 5.103

9.  Functional characterization of naturally occurring variants of human hepatitis B virus containing the core internal deletion mutation.

Authors:  T T Yuan; M H Lin; S M Qiu; C Shih
Journal:  J Virol       Date:  1998-03       Impact factor: 5.103

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.