Antiviral activity of nobiletin against chikungunya virus in vitro

被引:23
|
作者
Lin, Shih-Chao [1 ,2 ]
Chen, Mei-Chun [3 ]
Li, Shiming [4 ]
Lin, Chi-Chen [2 ,4 ,5 ,6 ,7 ]
Wang, Tony T. [3 ,8 ]
机构
[1] Natl Chung Hsing Univ, PhD Program Med Biotechnol, Taichung, Taiwan
[2] George Mason Univ, Nat Ctr Biodef & Infect Dis, Fairfax, VA 22030 USA
[3] SRI Int, Ctr Infect Dis, Discovery Biol, Harrisonburg, VA 22802 USA
[4] Huanggang Normal Univ, Hubei Collaborat Innovat Ctr Characterist Resour, Coll Life Sci, Hubei Key Lab Econ Forest Germplasm Improvement &, Huanggang, Peoples R China
[5] Natl Chung Hsing Univ, Inst Biomed Sci, Taichung, Taiwan
[6] Asia Univ, Dept Biotechnol, Taichung, Taiwan
[7] China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[8] Xinxiang Med Univ, Cent Hosp, Xinxiang, Peoples R China
基金
中国国家自然科学基金;
关键词
IMPROVES MEMORY IMPAIRMENT; LUNG-CANCER CELLS; INTERFERON-ALPHA; HUMAN BREAST; CITRUS; INFECTION; APOPTOSIS; DISEASE; MICE; COMBINATION;
D O I
10.3851/IMP3167
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Chikungunya virus (CHIKV), a highly contagious re-emerging virus, is transmitted by infected mosquitoes. CHIKV is prevalent in tropical countries and is continuing to creep farther north into temperate areas. CHIKV is responsible for induction of chikungunya fever (CF) and severe joint stiffness with the capability of developing into bilateral and systemic arthralgia or even encephalitis. Despite the high morbidity rate, no approved antiviral drug is available. Therefore, an anti-CHIKV therapy is necessary to control this disease. In this study, we screened four flavonoids for anti-CHIKV activities: nobiletin, phlorizin, resveratrol and oxyresveratrol. Methods: We performed MTT, Viral ToxGlo (TM) and lactate dehydrogenase (LDH) assays to assess the viability of CHIKV-infected host cells. Plaque assay and immunofluorescent assay were utilized to evaluate the levels of viral production in quantification and qualification, respectively. Results: We first confirmed that nobiletin can maintain the cellular survival of infected cells without inducing significant toxicity to host cells. Nobiletin suppressed virus-induced cell death and viral production. Also, the antiviral efficacy of nobiletin can last for at least 48 h during infection. More importantly, nobiletin inhibited CHIKV infection during the translation/replication stages and viral entry, making nobiletin a potential clinical antiviral agent in prophylaxis and post-exposure treatment. Conclusions: In this study, our results provided a strategy to develop anti-chikungunya agents by utilizing natural compounds. Also, we believe that nobiletin can be a potential antiviral agent against CHIKV infection worthy of being further investigated as a remedial candidate in vivo.
引用
收藏
页码:689 / 697
页数:9
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