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Identification and characterization of potent small molecule inhibitor of hemorrhagic fever New World arenaviruses

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 laborato...

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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114356/
https://www.ncbi.nlm.nih.gov/pubmed/16343651
http://dx.doi.org/10.1016/j.antiviral.2005.10.008
Descripción
Sumario: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 Junín 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 (Junín, 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.