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HIV protease inhibitor nelfinavir inhibits replication of SARS-associated coronavirus
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 inhibi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111005/ https://www.ncbi.nlm.nih.gov/pubmed/15144898 http://dx.doi.org/10.1016/j.bbrc.2004.04.083 |
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author | Yamamoto, Norio Yang, Rongge Yoshinaka, Yoshiyuki Amari, Shinji Nakano, Tatsuya Cinatl, Jindrich Rabenau, Holger Doerr, Hans Wilhelm Hunsmann, Gerhard Otaka, Akira Tamamura, Hirokazu Fujii, Nobutaka Yamamoto, Naoki |
author_facet | Yamamoto, Norio Yang, Rongge Yoshinaka, Yoshiyuki Amari, Shinji Nakano, Tatsuya Cinatl, Jindrich Rabenau, Holger Doerr, Hans Wilhelm Hunsmann, Gerhard Otaka, Akira Tamamura, Hirokazu Fujii, Nobutaka Yamamoto, Naoki |
author_sort | Yamamoto, Norio |
collection | PubMed |
description | 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 cytopathic 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 as a good lead compound for designing anti-SARS drugs. |
format | Online Article Text |
id | pubmed-7111005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71110052020-04-02 HIV protease inhibitor nelfinavir inhibits replication of SARS-associated coronavirus Yamamoto, Norio Yang, Rongge Yoshinaka, Yoshiyuki Amari, Shinji Nakano, Tatsuya Cinatl, Jindrich Rabenau, Holger Doerr, Hans Wilhelm Hunsmann, Gerhard Otaka, Akira Tamamura, Hirokazu Fujii, Nobutaka Yamamoto, Naoki Biochem Biophys Res Commun Article 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 cytopathic 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 as a good lead compound for designing anti-SARS drugs. Elsevier Inc. 2004-06-04 2004-05-06 /pmc/articles/PMC7111005/ /pubmed/15144898 http://dx.doi.org/10.1016/j.bbrc.2004.04.083 Text en Copyright © 2004 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Yamamoto, Norio Yang, Rongge Yoshinaka, Yoshiyuki Amari, Shinji Nakano, Tatsuya Cinatl, Jindrich Rabenau, Holger Doerr, Hans Wilhelm Hunsmann, Gerhard Otaka, Akira Tamamura, Hirokazu Fujii, Nobutaka Yamamoto, Naoki HIV protease inhibitor nelfinavir inhibits replication of SARS-associated coronavirus |
title | HIV protease inhibitor nelfinavir inhibits replication of SARS-associated coronavirus |
title_full | HIV protease inhibitor nelfinavir inhibits replication of SARS-associated coronavirus |
title_fullStr | HIV protease inhibitor nelfinavir inhibits replication of SARS-associated coronavirus |
title_full_unstemmed | HIV protease inhibitor nelfinavir inhibits replication of SARS-associated coronavirus |
title_short | HIV protease inhibitor nelfinavir inhibits replication of SARS-associated coronavirus |
title_sort | hiv protease inhibitor nelfinavir inhibits replication of sars-associated coronavirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111005/ https://www.ncbi.nlm.nih.gov/pubmed/15144898 http://dx.doi.org/10.1016/j.bbrc.2004.04.083 |
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