Category A arenaviruses as defined by the National Institute of Allergy and Infectious Diseases (NIAID) are human pathogens that could be weaponized by bioterrorists. Many of these deadly viruses require biosafety level-4 (BSL-4) containment for all laboratory work, which limits traditional laboratory high-throughput screening (HTS) for identification of small molecule inhibitors. For those reasons, a related BSL-2 New World arenavirus, Tacaribe virus, 67-78% identical to JunÃn virus at the amino acid level, was used in a HTS campaign where approximately 400,000 small molecule compounds were screened in a Tacaribe virus-induced cytopathic effect (CPE) assay. Compounds identified in this screen showed antiviral activity and specificity against not only Tacaribe virus, but also the Category A New World arenaviruses (JunÃn, Machupo, and Guanarito). Drug resistant variants were isolated, suggesting that these compounds act through inhibition of a viral protein, the viral glycoprotein (GP2), and not through cellular toxicity mechanisms. A lead compound, ST-294, has been chosen for drug development. This potent and selective compound, with good bioavailability, demonstrated protective anti-viral efficacy in a Tacaribe mouse challenge model. This series of compounds represent a new class of inhibitors that may warrant further development for potential inclusion in a strategic stockpile.
Identification and characterization of potent small molecule inhibitor of hemorrhagic fever New World arenaviruses.
鉴定和表征出血热新世界沙粒病毒的强效小分子抑制剂
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作者:Bolken Tove C, Laquerre Sylvie, Zhang Yuanming, Bailey Thomas R, Pevear Daniel C, Kickner Shirley S, Sperzel Lindsey E, Jones Kevin F, Warren Travis K, Amanda Lund S, Kirkwood-Watts Dana L, King David S, Shurtleff Amy C, Guttieri Mary C, Deng Yijun, Bleam Maureen, Hruby Dennis E
| 期刊: | Antiviral Research | 影响因子: | 4.000 |
| 时间: | 2006 | 起止号: | 2006 Feb;69(2):86-97 |
| doi: | 10.1016/j.antiviral.2005.10.008 | 研究方向: | 信号转导 |
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