共 24 条
SUSCEPTIBILITY OF HUMAN T-LYMPHOTROPIC VIRUS TYPE-I INFECTED CELL-LINE MT-2 TO HEPATITIS-C VIRUS-INFECTION
被引:109
作者:

KATO, N
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h-index: 0
机构: Natl Canc Ctr, Res Inst, Div Virol, Tokyo, 104, Chuo KU

NAKAZAWA, T
论文数: 0 引用数: 0
h-index: 0
机构: Natl Canc Ctr, Res Inst, Div Virol, Tokyo, 104, Chuo KU

MIZUTANI, T
论文数: 0 引用数: 0
h-index: 0
机构: Natl Canc Ctr, Res Inst, Div Virol, Tokyo, 104, Chuo KU

SHIMOTOHNO, K
论文数: 0 引用数: 0
h-index: 0
机构: Natl Canc Ctr, Res Inst, Div Virol, Tokyo, 104, Chuo KU
机构:
[1] Natl Canc Ctr, Res Inst, Div Virol, Tokyo, 104, Chuo KU
关键词:
D O I:
10.1006/bbrc.1995.1123
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 [生物化学与分子生物学];
081704 [应用化学];
摘要:
To obtain a hepatitis C virus (HCV) proliferation system, we examined the susceptibility of various cultured cell lines to HCV infection. We found that a human T-lymphotropic virus type I infected cell Line MT-2 was fairly sensitive to HCV infection. Using the polymerase chain reaction, intracellular positive-stranded HCV RNA was detected until at least 15 days postinoculation (p.i.). Intracellular negative-stranded HCV RNA was also detected at 10 days p.i., although not at 7 days p.i., suggesting that HCV is replicating in MT-2 cells 10 days p.i. Sequence analysis of hypervariable region 1 (HVR1) revealed that HVR1 sequences from cells 10 days p.i. had become homogeneous, although HVR1 sequences from the inoculum showed the typical quasi-species. We also found a lack of anti-HVR1 antibody against the HVR1 species which became homogeneous at 10 days p.i., although we easily detected antibody against the other HVR1 species obtained from the inoculum. These findings suggest that MT-2 cells are susceptible to HCV infection and are capable of supporting HCV replication. (C) 1995 Academic Press, Inc.
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页码:863 / 869
页数:7
相关论文
共 24 条
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机构: Laboratory of Infectious Diseases, NIAID, National Institutes of Health, Bethesda

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SHIMOTOHNO, K
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