In Vitro Evaluation of the Anti-Chikungunya Virus Activity of an Active Fraction Obtained from Euphorbia grandicornis Latex

被引:0
作者
Santiago-Cruz, Jose Angel [1 ]
Posadas-Mondragon, Araceli [1 ]
Perez-Juarez, Angelica [1 ]
Herrera-Gonzalez, Norma Estela [2 ]
Chin-Chan, Jose Miguel [3 ]
Aguilar-Gonzalez, Joab Eli [1 ]
Aguilar-Faisal, Jose Leopoldo [1 ]
机构
[1] Inst Politecn Nacl, Escuela Super Med, Lab Med Conservac Secc Estudios Posgrad & Invest, Colonia Casco Santo Tomas, Mexico City 11340, DF, Mexico
[2] Inst Politecn Nacl, Escuela Super Med, Lab Oncol Mol Secc Estudios Posgrad & Invest, Plan San Luis & Diaz Miron, Mexico City 11340, Mexico
[3] Univ Autonoma Campeche, Fac Ciencias Quim Biol, Lab Invest, Campeche 24039, Campeche, Mexico
来源
VIRUSES-BASEL | 2024年 / 16卷 / 12期
关键词
chikungunya virus; antiviral; cytotoxic; selectivity; cancer cells; Euphorbia grandicornis; latex; oleanolic acid; roburic acid; DISCOVERY; MANAGEMENT; EMERGENCE; PROTEIN; ASIA;
D O I
10.3390/v16121929
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chikungunya virus (CHIKV) is classified as a pathogen with the potential to cause a pandemic. This situation becomes more alarming since no approved drug exists to combat the virus. The present research aims to demonstrate the anti-CHIKV activity of molecules present in the latex of Euphorbia grandicornis. Therefore, a biodirected assay was carried out to find the molecules with anti-CHIKV activity. Extractions with hexane, dichloromethane, and methanol and subsequent purification by column chromatography were carried out to later evaluate cytotoxic activity by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay and antiviral activity by plaque assay. Our findings show that unlike the others, methanolic extract has a low cytotoxic effect and a good anti-CHIKV effect (EC50 = 26.41 mu g/mL), which increases when obtaining the purified active fraction (pAFeg1) (EC50 = 0.4835 mu g/mL). Time-of-addition suggests that the possible mechanism of action of pAFeg1 could be inhibiting any of the non-structural proteins of CHIKV. In addition, both the cytotoxic and anti-CHIKV activity of pAFeg1 demonstrate selectivity since it killed cancer cells and could not inhibit DENV2.
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页数:20
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