Replication of the hepatitis C virus in cell culture

被引:68
作者
Bartenschlager, R [1 ]
Kaul, A [1 ]
Sparacio, S [1 ]
机构
[1] Heidelberg Univ, Dept Mol Virol, Otto Meyerhof Zentrum, D-69120 Heidelberg, Germany
关键词
hepatitis C virus; HCV; replicons; adaptation; RNA replication; cell culture; antiviral therapy; positive strand RNA virus; Flaviviridae interferon-alpha;
D O I
10.1016/j.antiviral.2003.08.016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Studies of hepatitis C virus (HCV) replication in cell culture have been greatly facilitated by the development of genetically engineered viral genomes that are capable of self-amplifying to high levels in a human hepatoma cell line. Since the original description of this 'replicon' model in 1999, important improvements have been made. Most notably, cell culture adaptive mutations were identified in various non-structural proteins that enhance RNA replication by several orders of magnitude. More recently, the permissiveness of the host cell was determined as an additional important factor contributing to efficient RNA replication. These discoveries allowed the development of transient replication assays, selectable full length genomes and a variety of novel replicons that will be useful for basic studies and facilitate the development of antiviral drugs. Ultimately, the replicon system may help to decipher the molecular basis of interferon-alpha (IFN-alpha) resistance. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 102
页数:12
相关论文
共 95 条
[31]   A 2ND HEPATITIS-C VIRUS-ENCODED PROTEINASE [J].
GRAKOUI, A ;
MCCOURT, DW ;
WYCHOWSKI, C ;
FEINSTONE, SM ;
RICE, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (22) :10583-10587
[32]   The p7 protein of hepatitis C virus forms an ion channel that is blocked by the antiviral drug, Amantadine [J].
Griffin, SDC ;
Beales, LP ;
Clarke, DS ;
Worsfold, O ;
Evans, SD ;
Jaeger, J ;
Harris, MPG ;
Rowlands, DJ .
FEBS LETTERS, 2003, 535 (1-3) :34-38
[33]   Effect of alpha interferon on the hepatitis C virus replicon [J].
Guo, JT ;
Bichko, VV ;
Seeger, C .
JOURNAL OF VIROLOGY, 2001, 75 (18) :8516-8523
[34]   Characterization of RNA binding activity and RNA helicase activity of the hepatitis C virus NS3 protein [J].
Gwack, Y ;
Kim, DW ;
Han, JH ;
Choe, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (02) :654-659
[35]   Hepatitis C virus RNA synthesis in a cell-free system isolated from replicon-containing hepatoma cells [J].
Hardy, RW ;
Marcotrigiano, J ;
Blight, KJ ;
Majors, JE ;
Rice, CM .
JOURNAL OF VIROLOGY, 2003, 77 (03) :2029-2037
[36]   To interfere and to anti-interfere: The interplay between hepatitis C virus and interferon [J].
He, YP ;
Katze, MG .
VIRAL IMMUNOLOGY, 2002, 15 (01) :95-119
[37]   2 DISTINCT PROTEINASE ACTIVITIES REQUIRED FOR THE PROCESSING OF A PUTATIVE NONSTRUCTURAL PRECURSOR PROTEIN OF HEPATITIS-C VIRUS [J].
HIJIKATA, M ;
MIZUSHIMA, H ;
AKAGI, T ;
MORI, S ;
KAKIUCHI, N ;
KATO, N ;
TANAKA, T ;
KIMURA, K ;
SHIMOTOHNO, K .
JOURNAL OF VIROLOGY, 1993, 67 (08) :4665-4675
[38]   Hepatitis C virus nonstructural protein 4B is an integral endoplasmic reticulum membrane protein [J].
Hügle, T ;
Fehrmann, F ;
Bieck, E ;
Kohara, M ;
Kräusslich, HG ;
Rice, CM ;
Blum, HE ;
Moradpour, D .
VIROLOGY, 2001, 284 (01) :70-81
[39]   Selectable subgenomic and genome-length dicistronic RNAs derived from an infectious molecular clone of the HCV-N strain of hepatitis C virus replicate efficiently in cultured Huh7 cells [J].
Ikeda, M ;
Yi, MK ;
Li, K ;
Lemon, SA .
JOURNAL OF VIROLOGY, 2002, 76 (06) :2997-3006
[40]   HEPATITIS-C VIRUS PARTICLE DETECTED BY IMMUNOELECTRON MICROSCOPIC STUDY [J].
KAITO, M ;
WATANABE, S ;
TSUKIYAMAKOHARA, K ;
YAMAGUCHI, K ;
KOBAYASHI, Y ;
KONISHI, M ;
YOKOI, M ;
ISHIDA, S ;
SUZUKI, S ;
KOHARA, M .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :1755-1760