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Provedor de dados:  Ciência Rural
País:  Brazil
Título:  In vitro activity of six antiviral drugs against equid alphaherpesvirus type 1 indicates ganciclovir as promising drug for in vivo studies
Autores:  Oliveira,Amanda Lovato de
Cargnelutti,Juliana Felipetto
Mortari,Ana Paula Gnocato
Flores,Eduardo Furtado
Weiblen,Rudi
Data:  2018-01-01
Ano:  2018
Palavras-chave:  EHV-1
Plaque assay
Acyclovir
Ganciclovir
Foscarnet
Famciclovir
Vidarabine
Cidofovir
Resumo:  ABSTRACT: Equid alphaherpesvirus type 1 (EHV-1) is distributed worldwide and is a major agent of abortion, respiratory and neurological disease in horses. No specific treatment is available for EHV-1 infection, yet the potential of antiviral therapy has been explored. In this study we investigated the in vitro activity of Acyclovir, Ganciclovir, Foscarnet, Famciclovir, Vidarabina and Cidofovir against EHV-1. For this, the MTT test was performed, in which all the tested drugs showed no toxicity up to 200μg/mL. Subsequently, different drug concentrations were submitted to viral plaque reduction assays in cell culture. The selectivity index (SI) of the compounds was determined using the cytotoxic concentration for 50% of cells (CC50), obtained by MTT, and effective drug concentration to inhibit by 50% the number of viral plaques (EC50). Ganciclovir (SI: 490; EC50: 1.9 μg/mL) was the most efficient and safest drug against EHV-1, followed by Cidofovir (SI: 150, EC50: 5.7μg/mL), Acyclovir (SI: 37.4, EC50: 22.2μg/mL), Famciclovir (SI: 25.1, EC50: 24.5μg/mL), Vidarabine (SI: 12.2, EC50: 40.9μg/mL) and Foscarnet (SI: 6.9, EC50: 49.5 μg/mL), respectively. These results indicated that Ganciclovir (followed by Cidofovir), is a promising candidate for use in in vivo experiments.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-84782018001200450
Editor:  Universidade Federal de Santa Maria
Relação:  10.1590/0103-8478cr20180085
Formato:  text/html
Fonte:  Ciência Rural v.48 n.12 2018
Direitos:  info:eu-repo/semantics/openAccess
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