Nucleic acid sequence analysis of basal core promoter/precore/core region of hepatitis B virus isolated from chronic carriers of the virus from Kolkata, eastern India: Low frequency of mutation in the precore region

被引:38
作者
Banerjee, A
Banerjee, S
Chowdhury, A
Santra, A
Chowdhury, S
Roychowdhury, S
Panda, CK
Bhattacharya, SK
Chakravarty, R
机构
[1] ICMR Virus Unit, Kolkata 700010, India
[2] Indian Inst Chem Biol, Kolkata, India
[3] Postgrad Inst Med Educ & Res, Dept Gastroenterol, Kolkata, India
[4] Chittaranjan Natl Canc Inst, Kolkata, India
[5] Natl Inst Cholera & Enter Dis, Kolkata, India
关键词
hepatitis B virus; genotype; genomic mutations; basal core promoter; precore/core;
D O I
10.1159/000086066
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Objective: The aim of the present study was to characterize the predominant hepatitis B virus (HBV) strains and their molecular variants present in the HBV isolates of the different genotypes found among the chronic carriers of the virus in our community. Methods: Precore/core and core promoter regions of HBV DNA were amplified by polymerase chain reaction and then subjected to direct sequencing. Of the 64 hepatitis B surface antigen (HBsAg)-positive chronic HBV carriers investigated, 44 were HBeAg negative and 20 were HBeAg positive. Results: In addition to genotype D, which was the predominant genotype, 12 genotype C (18.7%) and 6 genotype A (9.4%) were also detected. Presence of T at nt 1858 has often been related to the development of precore stop mutation at nt 1896, while that of C has been related to the development of 1762-1764 double mutation. In our study group, 39 of the 44 HBeAg-negative samples have T1858. The precore stop codon mutation was found in only 8 (18%) of the HBeAg-negative samples. More than half of the HBeAg-negative samples had wild-type sequence in the precore region. The core promoter region could be sequenced from 40 samples, and 1762-1764 double mutation was detected in 13 (32.5%) of them. No significant changes could be detected in the core amino acid sequence of these isolates. Conclusion: The pattern of core promoter and precore mutation of HBV isolates in the present study is atypical and not in accordance with reports from other parts of the world, where genotype D and genotype C with T at codon 1858 are common. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:389 / 399
页数:11
相关论文
共 43 条
[1]   Ethnic India: A genomic view, with special reference to peopling and structure [J].
Basu, A ;
Mukherjee, N ;
Roy, S ;
Sengupta, S ;
Banerjee, S ;
Chakraborty, M ;
Dey, B ;
Roy, M ;
Roy, B ;
Bhattacharyya, NP ;
Roychoudhury, S ;
Majumder, PP .
GENOME RESEARCH, 2003, 13 (10) :2277-2290
[2]  
Bläckberg J, 2000, J MED VIROL, V60, P107, DOI 10.1002/(SICI)1096-9071(200002)60:2&lt
[3]  
107::AID-JMV1&gt
[4]  
3.0.CO
[5]  
2-T
[6]   Effects of a naturally occurring mutation in the hepatitis B virus basal core promoter on precore gene expression and viral replication [J].
Buckwold, VE ;
Xu, ZC ;
Chen, M ;
Yen, TSB ;
Ou, JH .
JOURNAL OF VIROLOGY, 1996, 70 (09) :5845-5851
[7]   VIRAL GENETIC-VARIATION - HEPATITIS-B VIRUS AS A CLINICAL EXAMPLE [J].
CARMAN, W ;
THOMAS, H ;
DOMINGO, E .
LANCET, 1993, 341 (8841) :349-353
[8]   HEPATITIS-B E-ANTIGEN NEGATIVE CHRONIC ACTIVE HEPATITIS - HEPATITIS-B VIRUS CORE MUTATIONS OCCUR PREDOMINANTLY IN KNOWN ANTIGENIC DETERMINANTS [J].
CARMAN, WF ;
THURSZ, M ;
HADZIYANNIS, S ;
MCINTYRE, G ;
COLMAN, K ;
GIOUSTOZ, A ;
FATTOVICH, G ;
ALBERTI, A ;
THOMAS, HC .
JOURNAL OF VIRAL HEPATITIS, 1995, 2 (02) :77-84
[9]   Hepatitis B virus core protein mutations are concentrated in B cell epitopes in progressive disease and in T helper cell epitopes during clinical remission [J].
Carman, WF ;
Boner, W ;
Fattovich, G ;
Colman, K ;
Dornan, ES ;
Thursz, M ;
Hadziyannis, S .
JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (05) :1093-1100
[10]  
CARMAN WF, 1989, LANCET, V2, P588