| Literature DB >> 18570972 |
Geoffrey Chase1, Tao Deng, Ervin Fodor, Bo Wah Leung, Daniel Mayer, Martin Schwemmle, George Brownlee.
Abstract
The viral RNA polymerase complex of influenza A virus consists of three subunits PB1, PB2 and PA. Recently, the cellular chaperone Hsp90 was shown to play a role in nuclear import and assembly of the trimeric polymerase complex by binding to PB1 and PB2. Here we show that Hsp90 inhibitors, geldanamycin or its derivative 17-AAG, delay the growth of influenza virus in cell culture resulting in a 1-2 log reduction in viral titre early in infection. We suggest that this is caused by the reduced half-life of PB1 and PB2 and inhibition of nuclear import of PB1 and PA which lead to reduction in viral RNP assembly. Hsp90 inhibitors may represent a new class of antiviral compounds against influenza viruses.Entities:
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Year: 2008 PMID: 18570972 DOI: 10.1016/j.virol.2008.04.040
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616