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Published in: Virology Journal 1/2015

Open Access 01-12-2015 | Research

Quinic acid derivatives inhibit dengue virus replication in vitro

Authors: Paula Rodrigues Zanello, Andrea Cristine Koishi, Celso de Oliveira Rezende Júnior, Larissa Albuquerque Oliveira, Adriane Antonia Pereira, Mauro Vieira de Almeida, Claudia Nunes Duarte dos Santos, Juliano Bordignon

Published in: Virology Journal | Issue 1/2015

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Abstract

Background

Dengue is the most prevalent arboviral disease in tropical and sub-tropical areas of the world. The incidence of infection is estimated to be 390 million cases and 25,000 deaths per year. Despite these numbers, neither a specific treatment nor a preventive vaccine is available to protect people living in areas of high risk.

Results

With the aim of seeking a treatment that can mitigate dengue infection, we demonstrated that the quinic acid derivatives known as compound 2 and compound 10 were effective against all four dengue virus serotypes and safe for use in a human hepatoma cell line (Huh7.5). Both compounds were non-virucidal to dengue virus particles and did not interfere with early steps of the dengue virus life cycle, including binding and internalization. Experiments using a replicon system demonstrated that compounds 2 and 10 impaired dengue virus replication in Huh7.5 cells. Additionally, the anti-dengue virus effects of the quinic acid derivatives were preserved in human peripheral blood mononuclear cells.

Conclusions

Taken together, these data suggest that quinic acid derivatives represent a novel chemical class of active compounds that could be used to combat dengue virus infection.
Appendix
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Metadata
Title
Quinic acid derivatives inhibit dengue virus replication in vitro
Authors
Paula Rodrigues Zanello
Andrea Cristine Koishi
Celso de Oliveira Rezende Júnior
Larissa Albuquerque Oliveira
Adriane Antonia Pereira
Mauro Vieira de Almeida
Claudia Nunes Duarte dos Santos
Juliano Bordignon
Publication date
01-12-2015
Publisher
BioMed Central
Published in
Virology Journal / Issue 1/2015
Electronic ISSN: 1743-422X
DOI
https://doi.org/10.1186/s12985-015-0443-9

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