The pre-S region determines the intracellular localization and appearance of hepatitis B virus

被引:49
作者
Bock, CT [1 ]
Tillmann, HL [1 ]
Manns, MP [1 ]
Trautwein, C [1 ]
机构
[1] Med Hsch Hannover, Dept Gastroenterol & Hepatol, D-30625 Hannover, Germany
关键词
D O I
10.1002/hep.510300206
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The functional role of the hepatitis B virus (HBV) pre-S region for assembly and appearance of the virus is not completely understood. In this study, 3 natural-occurring mutants were investigated. Three mutants of the pre-S region-a point mutation in the CCAAT box (MUT1), a 6-bp deletion (MUT2) 3' of the CCAAT box, and a 153-bp deletion (MUT3) in the preS2 domain-were cloned alone or in combinations in replication-competent HBV plasmids and transfected in hepatoma cells. The impact on HBV assembly and appearance was studied by Northern Blot, primer extension analysis, immunofluorescence studies, enzyme-linked immunosorbent assay, and electron microscopy. An inversed ratio of pre-S/S mRNA transcripts compared with wild-type (wt) HBV was found when either MUT1 or -2 were included into the plasmid. Intracellular localization with both mutants showed retention of large S-protein in the endoplasmic reticulum and nuclear accumulation of core protein. The extracellular amount of S-protein was reduced with MUT1 and -2 or combinations in which 1 of the mutants was included. However, the extracellular appearance of viral products was comparable with wtHBV. In contrast, MUT3 showed major changes. Virion-like particles had a fried-egg, and filaments a screw-like appearance. The S-promoter mutations MUT1 and MUT2 correlated with viral retention. MUT3 leads to malformed viral particles. Therefore, different regions in the pre-S domain are essential to determine the intracellular localization and extracellular appearance of HBV, and might contribute to the prognosis of chronic HBV infection.
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页码:517 / 525
页数:9
相关论文
共 40 条
[1]
CONTROLLED SYNTHESIS OF HBSAG IN A DIFFERENTIATED HUMAN-LIVER CARCINOMA-DERIVED CELL-LINE [J].
ADEN, DP ;
FOGEL, A ;
PLOTKIN, S ;
DAMJANOV, I ;
KNOWLES, BB .
NATURE, 1979, 282 (5739) :615-616
[2]
A PreS mutation isolated from a patient with chronic hepatitis B infection leads to virus retention and misassembly [J].
Bock, CT ;
Tillmann, HL ;
Maschek, HJ ;
Manns, MP ;
Trautwein, C .
GASTROENTEROLOGY, 1997, 113 (06) :1976-1982
[3]
HEPATITIS-B VIRUS GENOME IS ORGANIZED INTO NUCLEOSOMES IN THE NUCLEUS OF THE INFECTED CELL [J].
BOCK, CT ;
SCHRANZ, P ;
SCHRODER, CH ;
ZENTGRAF, H .
VIRUS GENES, 1994, 8 (03) :215-229
[4]
Localization of hepatitis B virus core protein and viral DNA at the nuclear membrane [J].
Bock, CT ;
Schwinn, S ;
Schroder, CH ;
Velhagen, I ;
Zentgraf, H .
VIRUS GENES, 1996, 12 (01) :53-63
[5]
MAPPING A REGION OF THE LARGE ENVELOPE PROTEIN REQUIRED FOR HEPATITIS-B VIRION MATURATION [J].
BRUSS, V ;
THOMSSEN, R .
JOURNAL OF VIROLOGY, 1994, 68 (03) :1643-1650
[7]
POSTTRANSLATIONAL ALTERATIONS IN TRANSMEMBRANE TOPOLOGY OF THE HEPATITIS-B VIRUS LARGE ENVELOPE PROTEIN [J].
BRUSS, V ;
LU, XY ;
THOMSSEN, R ;
GERLICH, WH .
EMBO JOURNAL, 1994, 13 (10) :2273-2279
[8]
FUNCTIONS OF THE INTERNAL PRE-S DOMAIN OF THE LARGE SURFACE PROTEIN IN HEPATITIS-B VIRUS PARTICLE MORPHOGENESIS [J].
BRUSS, V ;
VIELUF, K .
JOURNAL OF VIROLOGY, 1995, 69 (11) :6652-6657
[9]
THE ROLE OF ENVELOPE PROTEINS IN HEPATITIS-B VIRUS ASSEMBLY [J].
BRUSS, V ;
GANEM, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (03) :1059-1063
[10]
Hepatitis B virus envelope variation after transplantation with and without hepatitis B immune globulin prophylaxis [J].
Carman, WF ;
Trautwein, C ;
vanDeursen, FJ ;
Colman, K ;
Dornan, E ;
McIntyre, G ;
Waters, J ;
Kliem, V ;
Muller, R ;
Thomas, HC ;
Mannis, MP .
HEPATOLOGY, 1996, 24 (03) :489-493