HIV protease inhibitor nelfinavir inhibits replication of SARS-associated coronavirus

被引:229
作者
Yamamoto, N
Yang, RG
Yoshinaka, Y
Amari, S
Nakano, T
Cinatl, J
Rabenau, H
Doerr, HW
Hunsmann, G
Otaka, A
Tamamura, H
Fujii, N
Yamamoto, N
机构
[1] Tokyo Med & Dent Univ, Grad Sch, Dept Mol Virol, Bunkyo Ku, Tokyo 1138519, Japan
[2] Univ Tokyo, Inst Ind Sci, Collaborat Res Ctr Frontier Simulat Software Ind, Meguro Ku, Tokyo 1538505, Japan
[3] Natl Inst Hlth Sci, Div Safety Informat Drug Food & Chem, Setagaya Ku, Tokyo 1588501, Japan
[4] Goethe Univ Frankfurt, Sch Med, Inst Med Virol, D-60596 Frankfurt, Germany
[5] German Primate Ctr, Dept Virol & Immunol, D-37077 Gottingen, Germany
[6] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
关键词
severe acute respiratory syndrome; coronavirus; HIV protease inhibitor;
D O I
10.1016/j.bbrc.2004.04.083
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
A novel coronavirus has been identified as an etiological agent of severe acute respiratory syndrome (SARS). To rapidly identify anti-SARS drugs available for clinical use. we screened a set of compounds that included antiviral drugs already in wide use. Here, we report that the HIV-1 protease inhibitor, nelfinavir, strongly inhibited replication of the SARS coronavirus (SARS-CoV). Nelfinavir inhibited the cylopathic effect induced by SARS-CoV infection. Expression of viral antigens was much lower in infected cells treated with nelfinavir than in untreated infected cells. Quantitative RT-PCR analysis showed that nelfinavir could decrease the production of virions from Vero cells. Experiments with various timings of drug addition revealed that nelfinavir exerted its effect not at the entry step, but at the post-entry step of SARS-CoV infection. Our results suggest that nelfinavir should be examined clinically for the treatment of SARS and has potential is a good lead compound for designing anti-SARS drugs. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:719 / 725
页数:7
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