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The Plant-Derived Naphthoquinone Droserone Inhibits In Vitro Measles Virus Infection.
Lieberherr, Christina; Zhang, Guoliang; Grafen, Anika; Singethan, Katrin; Kendl, Sabine; Vogt, Valentin; Maier, Jonathan; Bringmann, Gerhard; Schneider-Schaulies, Jürgen.
Afiliação
  • Lieberherr C; Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
  • Zhang G; Institute of Organic Chemistry, University of Würzburg, Würzburg, Germany.
  • Grafen A; Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
  • Singethan K; Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
  • Kendl S; Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
  • Vogt V; Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
  • Maier J; Institute of Organic Chemistry, University of Würzburg, Würzburg, Germany.
  • Bringmann G; Institute of Organic Chemistry, University of Würzburg, Würzburg, Germany.
  • Schneider-Schaulies J; Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
Planta Med ; 83(3-04): 232-238, 2017 Feb.
Article em En | MEDLINE | ID: mdl-27420351
ABSTRACT
The naphthoquinone droserone (1) is a natural product occurring in dicotyledonous plants. We have now observed that the addition of 1 during infection of tissue culture cells with measles virus considerably reduced the infection. Interestingly, the infection was inhibited only when droserone (1) was added during virus entry, but not when added to the cells prior to virus uptake or after virus uptake. These findings suggest that 1 interacts with viral particles to reduce infectivity. The formation of progeny measles virus particles was inhibited to 50 % by droserone (1) at a concentration (IC50) of approximately 2 µM with a half-maximal cytotoxicity (CC50) of about 60 µM for Vero cells. Other tested naphthoquinone derivatives, among them the likewise natural plumbagin (2), but also synthetic analogs, were either more cytotoxic or not as effective as 1. Thus, our data do not support the development of naphthoquinone derivatives into antiviral compounds, but suggest that they may be interesting research tools to study measles virus entry into cells.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Naftoquinonas / Sarampo / Vírus do Sarampo Limite: Animals Idioma: En Revista: Planta Med Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Naftoquinonas / Sarampo / Vírus do Sarampo Limite: Animals Idioma: En Revista: Planta Med Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha