Arbidol (Umifenovir): A Broad-Spectrum Antiviral Drug That Inhibits Medically Important Arthropod-Borne Flaviviruses

被引:107
作者
Haviernik, Jan [1 ]
Stefanik, Michal [1 ]
Fojtikova, Martina [1 ]
Kali, Sabrina [2 ]
Tordo, Noel [2 ,3 ]
Rudolf, Ivo [4 ]
Hubalek, Zdenek [4 ]
Eyer, Ludek [1 ,5 ]
Ruzek, Daniel [1 ,5 ]
机构
[1] Vet Res Inst, Dept Virol, Hudcova 70, CZ-62100 Brno, Czech Republic
[2] Inst Pasteur, Unit Antiviral Strategies, 25 Dr Roux, F-75724 Paris 15, France
[3] Inst Pasteur Guinee, Route Donka, Conakry, Guinea
[4] Czech Acad Sci, Inst Vertebrate Biol, Kvetna 8, CZ-60365 Brno, Czech Republic
[5] Czech Acad Sci, Biol Ctr, Inst Parasitol, Branisovska 31, CZ-37005 Ceske Budejovice, Czech Republic
来源
VIRUSES-BASEL | 2018年 / 10卷 / 04期
基金
欧盟地平线“2020”;
关键词
flavivirus; arbidol; umifenovir; antiviral activity; cytotoxicity; cell-type dependent antiviral effect; NUCLEOSIDE INHIBITORS; ZIKA VIRUS; IN-VITRO; EFFICACY; SOFOSBUVIR; MECHANISM; COMPOUND; CULTURE; MODEL;
D O I
10.3390/v10040184
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Arthropod-borne flaviviruses are human pathogens of global medical importance, against which no effective small molecule-based antiviral therapy has currently been reported. Arbidol (umifenovir) is a broad-spectrum antiviral compound approved in Russia and China for prophylaxis and treatment of influenza. This compound shows activities against numerous DNA and RNA viruses. The mode of action is based predominantly on impairment of critical steps in virus-cell interactions. Here we demonstrate that arbidol possesses micromolar-level anti-viral effects (EC50 values ranging from 10.57 +/- 0.74 to 19.16 +/- 0.29 mu M) in Vero cells infected with Zika virus, West Nile virus, and tick-borne encephalitis virus, three medically important representatives of the arthropod-borne flaviviruses. Interestingly, no antiviral effects of arbidol are observed in virus infected porcine stable kidney cells (PS), human neuroblastoma cells (UKF-NB-4), and human hepatoma cells (Huh-7 cells) indicating that the antiviral effect of arbidol is strongly cell-type dependent. Arbidol shows increasing cytotoxicity when tested in various cell lines, in the order: Huh-7 < HBCA < PS < UKF-NB-4 < Vero with CC50 values ranging from 18.69 +/- 0.1 to 89.72 +/- 0.19 mu M. Antiviral activities and acceptable cytotoxicity profiles suggest that arbidol could be a promising candidate for further investigation as a potential therapeutic agent in selective treatment of flaviviral infections.
引用
收藏
页数:8
相关论文
共 33 条
[1]
Baier A., 2011, FLAVIVIRUS ENCEPHALI, P89
[2]
Monitoring of didanosine and stavudine intracellular trisphosphorylated anabolite concentrations in HIV-infected patients [J].
Becher, F ;
Landman, R ;
Mboup, S ;
Kane, CNT ;
Canestri, A ;
Liegeois, F ;
Vray, M ;
Prevot, MH ;
Leleu, G ;
Benech, H .
AIDS, 2004, 18 (02) :181-187
[3]
Arbidol:: A broad-spectrum antiviral compound that blocks viral fusion [J].
Boriskin, Y. S. ;
Leneva, I. A. ;
Pecheur, E. -I. ;
Polyak, S. J. .
CURRENT MEDICINAL CHEMISTRY, 2008, 15 (10) :997-1005
[4]
Arbidol:: a broad-spectrum antiviral that inhibits acute and chronic HCV infection [J].
Boriskin, Yury S. ;
Pecheur, Eve-Isabelle ;
Polyak, Stephen J. .
VIROLOGY JOURNAL, 2006, 3 (1)
[5]
Virus morphogenesis and viral entry as alternative targets for novel hepatitis C antivirals [J].
Chapel, Cynthia ;
Zitzmann, Nicole ;
Zoulim, Fabien ;
Durantel, David .
FUTURE VIROLOGY, 2006, 1 (02) :197-209
[6]
In vitro antiviral activity of arbidol against Chikungunya virus and characteristics of a selected resistant mutant [J].
Delogu, Ilenia ;
Pastorino, Boris ;
Baronti, Cecile ;
Nougairede, Antoine ;
Bonnet, Emilie ;
de Lamballerie, Xavier .
ANTIVIRAL RESEARCH, 2011, 90 (03) :99-107
[7]
DEMADRID AT, 1969, B WORLD HEALTH ORGAN, V40, P113
[8]
Efficacy of arbidol on lethal hantaan virus infections in suckling mice and in vitro [J].
Deng, Hai-ying ;
Luo, Fan ;
Shi, Li-qiao ;
Zhong, Qiong ;
Liu, Ying-juan ;
Yang, Zhan-qiu .
ACTA PHARMACOLOGICA SINICA, 2009, 30 (07) :1015-1024
[9]
Adenosine Analog NITD008 Is a Potent Inhibitor of Zika Virus [J].
Deng, Yong-Qiang ;
Zhang, Na-Na ;
Li, Chun-Feng ;
Tian, Min ;
Hao, Jia-Nan ;
Xie, Xu-Ping ;
Shi, Pei-Yong ;
Qin, Cheng-Feng .
OPEN FORUM INFECTIOUS DISEASES, 2016, 3 (04)
[10]
Eyer Ludek, 2018, Antiviral Chemistry & Chemotherapy, V26, DOI 10.1177/2040206618761299