Antiviral activity of silymarin against chikungunya virus

被引:97
作者
Lani, Rafidah [1 ]
Hassandarvish, Pouya [1 ]
Chiam, Chun Wei [1 ]
Moghaddam, Ehsan [1 ]
Chu, Justin Jang Hann [2 ]
Rausalu, Kai [3 ]
Merits, Andres [3 ]
Higgs, Stephen [4 ]
Vanlandingham, Dana [5 ]
Abu Bakar, Sazaly [1 ]
Zandi, Keivan [1 ]
机构
[1] Univ Malaya, Fac Med, Dept Med Microbiol, Trop Infect Dis Res & Educ Ctr, Kuala Lumpur, Malaysia
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Microbiol, Lab Mol RNA Virol & Antiviral Strategies, Singapore 117595, Singapore
[3] Univ Tartu, Inst Technol, EE-50090 Tartu, Estonia
[4] Kansas State Univ, Biosecur Res Inst, Manhattan, KS 66506 USA
[5] Kansas State Univ, Dept Diagnost Med & Pathobiol, Manhattan, KS 66506 USA
关键词
REPLICATION; STRAND; ARBIDOL; ENTRY; RNA;
D O I
10.1038/srep11421
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
The mosquito-borne chikungunya virus (CHIKV) causes chikungunya fever, with clinical presentations such as severe back and small joint pain, and debilitating arthritis associated with crippling pains that persist for weeks and even years. Although there are several studies to evaluate the efficacy of drugs against CHIKV, the treatment for chikungunya fever is mainly symptom-based and no effective licensed vaccine or antiviral are available. Here, we investigated the antiviral activity of three types of flavonoids against CHIKV in vitro replication. Three compounds: silymarin, quercetin and kaempferol were evaluated for their in vitro antiviral activities against CHIKV using a CHIKV replicon cell line and clinical isolate of CHIKV of Central/East African genotype. A cytopathic effect inhibition assay was used to determine their activities on CHIKV viral replication and quantitative reverse transcription PCR was used to calculate virus yield. Antiviral activity of effective compound was further investigated by evaluation of CHIKV protein expression using western blotting for CHIKV nsP1, nsP3, and E2E1 proteins. Briefly, silymarin exhibited significant antiviral activity against CHIKV, reducing both CHIKV replication efficiency and down-regulating production of viral proteins involved in replication. This study may have important consequence for broaden the chance of getting the effective antiviral for CHIKV infection.
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页数:10
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