Nonstructural protein 5A does not contribute to the resistance of hepatitis C virus replication to interferon alpha in cell culture

被引:12
|
作者
Siepen, MAD
Lohmann, V
Wiese, M
Ross, S
Roggendorf, M
Viazov, S
机构
[1] Essen Univ Hosp, Inst Virol, D-45122 Essen, Germany
[2] Heidelberg Univ, Dept Vasc Virol, D-69120 Heidelberg, Germany
[3] Gen Hosp St Georg, D-04129 Leipzig, Germany
关键词
HCV; NS5A; IFN-alpha;
D O I
10.1016/j.virol.2005.03.012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The hepatitis C virus (HCV) subgenomic replicon system was used to study a possible involvement of nonstructural protein 5A (NS5A) in the mechanisms of HCV resistance to interferon alpha (IFN-alpha). A series of chimeric HCV replicons was constructed. In these replicons, the NS5A gene in the backbone of the Con1 replicon was swapped by corresponding fragments obtained from four IFN-alpha, responder and four IFN-alpha nonresponder patients that had been infected with the same HCV AD78 strain. Experiments with transfected Huh7 cells did not reveal significant differences in sensitivity of HCV RNA replication to IFN-alpha in cell clones, hearing chimeric Con1/AD78 replicons with NS5A sequences from IFN responders and nonresponders. Thus, these data provide no evidence that the NS5A protein contributes to the resistance of HCV replication to IFN-alpha. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:131 / 136
页数:6
相关论文
共 50 条
  • [31] Mutations in the nonstructural 5A gene of European hepatitis C virus isolates and response to interferon Alfa
    Zeuzem, S
    Lee, JH
    Roth, WK
    HEPATOLOGY, 1997, 25 (03) : 740 - 744
  • [32] Hepatitis C virus nonstructural protein 5A (NS5A) is an RNA-binding protein
    Huang, LY
    Hwang, J
    Sharma, SD
    Hargittai, MRS
    Chen, YF
    Arnold, JJ
    Raney, KD
    Cameron, CE
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (43) : 36417 - 36428
  • [33] Statistical analysis of combined substitutions in nonstructural 5A region of hepatitis C virus and interferon response
    Witherell, GW
    Beineke, P
    JOURNAL OF MEDICAL VIROLOGY, 2001, 63 (01) : 8 - 16
  • [34] Mutations in the interferon-sensitivity determining region of hepatitis C virus and transcriptional activity of the nonstructural region 5A protein
    Fukuma, T
    Enomoto, N
    Marumo, F
    Sato, C
    HEPATOLOGY, 1998, 28 (04) : 1147 - 1153
  • [35] Control of temporal activation of hepatitis C virus-induced interferon response by domain 2 of nonstructural protein 5A
    Hiet, Marie-Sophie
    Bauhofer, Oliver
    Zayas, Margarita
    Roth, Hanna
    Tanaka, Yasuhito
    Schirmacher, Peter
    Willemsen, Joschka
    Gruenvogel, Oliver
    Bender, Silke
    Binder, Marco
    Lohmann, Volker
    Lotteau, Vincent
    Ruggieri, Alessia
    Bartenschlager, Ralf
    JOURNAL OF HEPATOLOGY, 2015, 63 (04) : 829 - 837
  • [36] Hepatitis C Virus Nonstructural Protein 5A Inhibits Thapsigargin-Induced Apoptosis
    Jiang, Xia
    Kanda, Tatsuo
    Wu, Shuang
    Nakamoto, Shingo
    Wakita, Takaji
    Shirasawa, Hiroshi
    Yokosuka, Osamu
    PLOS ONE, 2014, 9 (11):
  • [37] Viral evolution and interferon resistance of hepatitis C virus RNA replication in a cell culture model
    Sumpter, R
    Wang, CF
    Foy, E
    Loo, YM
    Gale, M
    JOURNAL OF VIROLOGY, 2004, 78 (21) : 11591 - 11604
  • [38] Hepatitis C virus nonstructural protein 5A contains potential transcriptional activator domains
    Chung, KM
    Song, OK
    Jang, SK
    MOLECULES AND CELLS, 1997, 7 (05) : 661 - 667
  • [39] Pim Kinase Interacts with Nonstructural 5A Protein and Regulates Hepatitis C Virus Entry
    Park, Chorong
    Min, Saehong
    Park, Eun-Mee
    Lim, Yun-Sook
    Kang, Sangmin
    Suzuki, Tetsuro
    Shin, Eui-Cheol
    Hwang, Soon B.
    JOURNAL OF VIROLOGY, 2015, 89 (19) : 10073 - 10086
  • [40] Structure and function of the membrane anchor domain of hepatitis C virus nonstructural protein 5A
    Penin, F
    Brass, V
    Appel, N
    Ramboarina, S
    Montserret, R
    Ficheux, D
    Blum, HE
    Bartenschlager, R
    Moradpour, D
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (39) : 40835 - 40843