共 33 条
MEK inhibition impairs influenza B virus propagation without emergence of resistant variants
被引:111
作者:

Ludwig, S
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机构: Univ Dusseldorf, Inst Mol Med, D-40225 Dusseldorf, Germany

Wolff, T
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机构: Univ Dusseldorf, Inst Mol Med, D-40225 Dusseldorf, Germany

Ehrhardt, C
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h-index: 0
机构: Univ Dusseldorf, Inst Mol Med, D-40225 Dusseldorf, Germany

Wurzer, WJ
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h-index: 0
机构: Univ Dusseldorf, Inst Mol Med, D-40225 Dusseldorf, Germany

Reinhardt, J
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机构: Univ Dusseldorf, Inst Mol Med, D-40225 Dusseldorf, Germany

Planz, O
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机构: Univ Dusseldorf, Inst Mol Med, D-40225 Dusseldorf, Germany

Pleschka, S
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机构: Univ Dusseldorf, Inst Mol Med, D-40225 Dusseldorf, Germany
机构:
[1] Univ Dusseldorf, Inst Mol Med, D-40225 Dusseldorf, Germany
[2] Univ Wurzburg, MSZ, D-97078 Wurzburg, Germany
[3] Robert Koch Inst, D-13353 Berlin, Germany
[4] BFAV, Inst Immunol, D-72076 Tubingen, Germany
[5] Univ Giessen, Fachbereich Vet Med, Inst Virol, D-35392 Giessen, Germany
关键词:
influenza virus;
mitogen-activated protein kinase cascade;
mitogen-activated protein kinase/extracellular;
signal-regulated kinase inhibition;
viral resistance;
D O I:
10.1016/S0014-5793(04)00108-5
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Influenza A and B viruses are still a major worldwide threat. We demonstrate that influenza B virus infection induces signaling via the Raf/MEK/ERK cascade, a process required for efficient virus production. Expression of dominant-negative Raf and ERK mutants or treatment with a MEK inhibitor (U0126) strongly impaired viral propagation, while selective activation of the pathway resulted in increased virus titers. MEK inhibition appears to interfere with a distinct viral nuclear export process. Most importantly, no resistant virus variants emerged in the presence of U0126 demonstrating that influenza viruses cannot easily adapt to the missing cellular function. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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页码:37 / 43
页数:7
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