The citrus flavanone naringenin impairs dengue virus replication in human cells

被引:105
作者
Frabasile, Sandra [1 ,2 ]
Koishi, Andrea Cristine [2 ]
Kuczera, Diogo [2 ]
Silveira, Guilherme Ferreira [2 ]
Verri, Waldiceu Aparecido, Jr. [3 ]
Duarte dos Santos, Claudia Nunes [1 ]
Bordignon, Juliano [1 ]
机构
[1] Univ Republica, Fac Ciencias, Secc Virol, Montevideo 11400, Uruguay
[2] Inst Carlos Chagas, Mol Virol Lab, ICC FIOCRUZ PR, Curitiba, Parana, Brazil
[3] Univ Estadual Londrina, Ctr Ciencias Biol, Dept Ciencias Patol, Londrina, Parana, Brazil
关键词
ANTIVIRAL ACTIVITY; INFLAMMATORY PAIN; IN-VITRO; FLAVONOIDS; INHIBITION; TYPE-1;
D O I
10.1038/srep41864
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dengue is one of the most significant health problems in tropical and sub-tropical regions throughout the world. Nearly 390 million cases are reported each year. Although a vaccine was recently approved in certain countries, an anti-dengue virus drug is still needed. Fruits and vegetables may be sources of compounds with medicinal properties, such as flavonoids. This study demonstrates the anti-dengue virus activity of the citrus flavanone naringenin, a class of flavonoid. Naringenin prevented infection with four dengue virus serotypes in Huh7.5 cells. Additionally, experiments employing subgenomic RepDV-1 and RepDV-3 replicon systems confirmed the ability of naringenin to inhibit dengue virus replication. Antiviral activity was observed even when naringenin was used to treat Huh7.5 cells 24 h after dengue virus exposure. Finally, naringenin anti-dengue virus activity was demonstrated in primary human monocytes infected with dengue virus sertoype-4, supporting the potential use of naringenin to control dengue virus replication. In conclusion, naringenin is a suitable candidate molecule for the development of specific dengue virus treatments.
引用
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页数:10
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