Enhanced intracellular retention of a hepatitis B virus strain associated with fulminant hepatitis

被引:31
作者
Inoue, Jun [1 ]
Ueno, Yoshiyuki [1 ]
Nagasaki, Futoshi [1 ]
Wakui, Yuta [1 ]
Kondo, Yasuteru [1 ]
Fukushima, Koji [1 ]
Niitsuma, Hirofumi [1 ]
Shimosegawa, Tooru [1 ]
机构
[1] Tohoku Univ, Div Gastroenterol, Grad Sch Med, Aoba Ku, Sendai, Miyagi 9808574, Japan
关键词
HBV; Mutation; Core promoter; Precore; A1762T/G1764A; G1862T; G1896A; Replicative intermediates; HBcAg; CORE PROMOTER MUTATIONS; PRECORE REGION; E-ANTIGEN; VIRAL REPLICATION; X GENE; DNA; PROTEIN; EXPRESSION; APOPTOSIS; CELLS;
D O I
10.1016/j.virol.2009.09.028
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A plasmid carrying 1.3-fold HBV genome was constructed from a HBV strain that caused five consecutive cases of fulminant hepatitis (pBFH2), and HepG2 cells were transfected with pBFH2 or its variants. The pBFH2 construct with A1762T/G1764A, G1862T, and G1896A showed the largest amount of core particle-associated intracellular HBV DNA, but no significant increase of extracellular HBV DNA in comparison with the wild construct, suggesting that these mutations might work together for retention of the replicative intermediates in the cells. The retention might relate to the localization of hepatitis B core antigen (HBcAg) in the nucleus of HepG2, which was observed by confocal fluorescence microscopy. HBcAg immunohistochemical examination of liver tissue samples obtained from the consecutive fulminant hepatitis patients showed stronger staining in the nucleus than acute hepatitis patients. In conclusion, the fulminant HBV strain caused retention of the core particles and the core particle-associated HBV DNA in the cells. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:202 / 209
页数:8
相关论文
共 41 条
[1]   Rebound of hepatitis B virus replication in HepG2 cells after cessation of antiviral treatment [J].
Abdelhamed, AM ;
Kelley, CM ;
Miller, TG ;
Furman, PA ;
Isom, HC .
JOURNAL OF VIROLOGY, 2002, 76 (16) :8148-8160
[2]   Two core promotor mutations identified in a hepatitis B virus strain associated with fulminant hepatitis result in enhanced viral replication [J].
Baumert, TF ;
Rogers, SA ;
Hasegawa, K ;
Liang, TJ .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (10) :2268-2276
[3]   Hepatitis B virus mutations associated with fulminant hepatitis induce apoptosis in primary Tupaia hepatocytes [J].
Baumert, TF ;
Yang, C ;
Schürmann, P ;
Köck, J ;
Ziegler, C ;
Grüllich, C ;
Nassal, M ;
Liang, TJ ;
Blum, HE ;
von Weizsäcker, F .
HEPATOLOGY, 2005, 41 (02) :247-256
[4]   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
[5]  
CARMAN WF, 1989, LANCET, V2, P588
[6]   A valine to phenylalanine mutation in the precore region of hepatitis B virus causes intracellular retention and impaired secretion of HBe-antigen [J].
Chen, Chien Yu ;
Crowther, Carol ;
Kew, Michael C. ;
Kramvis, Anna .
HEPATOLOGY RESEARCH, 2008, 38 (06) :580-592
[7]   The hepatitis B virus X gene induces p53-mediated programmed cell death [J].
Chirillo, P ;
Pagano, S ;
Natoli, G ;
Puri, PL ;
Burgio, VL ;
Balsano, C ;
Levrero, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :8162-8167
[8]   Cytotoxic T cells and viral hepatitis [J].
Chisari, FV .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (07) :1472-1477
[9]   Characterization of a conformational epitope on hepatitis B virus core antigen and quasiequivalent variations in antibody binding [J].
Conway, JF ;
Watts, NR ;
Belnap, DM ;
Cheng, N ;
Stahl, SJ ;
Wingfield, PT ;
Steven, AC .
JOURNAL OF VIROLOGY, 2003, 77 (11) :6466-6473
[10]   Cellular vacuolization and apoptosis induced by hepatitis B virus large surface protein [J].
Foo, NC ;
Ahn, BY ;
Ma, XH ;
Hyun, W ;
Yen, TSB .
HEPATOLOGY, 2002, 36 (06) :1400-1407