Paulownin triazole-chloroquinoline derivative: a promising antiviral candidate against chikungunya virus.

IF 2.1 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Adriana Cotta Cardoso Reis, Camila Mendes de Oliveira, Beatriz Carvalho Rangel, Laura Vogas Bonsucesso de Carvalho, Camila Portruneli, Livia da Cunha Agostini, Isadora Oliveira Ansaloni Pereira, Breno de Mello Silva, Cíntia Lopes de Brito Magalhães, Glenda Nicioli da Silva, Guilherme Rocha Pereira, Geraldo Célio Brandão
{"title":"Paulownin triazole-chloroquinoline derivative: a promising antiviral candidate against chikungunya virus.","authors":"Adriana Cotta Cardoso Reis, Camila Mendes de Oliveira, Beatriz Carvalho Rangel, Laura Vogas Bonsucesso de Carvalho, Camila Portruneli, Livia da Cunha Agostini, Isadora Oliveira Ansaloni Pereira, Breno de Mello Silva, Cíntia Lopes de Brito Magalhães, Glenda Nicioli da Silva, Guilherme Rocha Pereira, Geraldo Célio Brandão","doi":"10.1093/lambio/ovaf092","DOIUrl":null,"url":null,"abstract":"<p><p>Viral infections, including arboviruses such as chikungunya, zika, dengue, and mayaro fever, remain significant global health and economic challenges, fueled by the emergence and resurgence of mosquito-borne diseases. Natural products, especially plant-derived compounds, have been crucial in drug discovery and often serve as scaffolds for synthetic drug development. This study focused on modifying paulownin, an isolated lignan, through a Click reaction to incorporate 1,2,3-triazole and quinolinic ring frameworks. The resulting derivative 7 was evaluated for its in vitro antiviral activity against Alphavirus chikungunya (CHIKV). The paulownin derivative 7 did not exhibit cytotoxicity in Vero cells and demonstrated potent activity against CHIKV, with median effective concentration value of 9.05 µM and a selectivity index exceeding 16.8. Furthermore, compound 7 outperformed positive controls, being over 46 times more active against CHIKV. Cytopathic effect assays confirmed this anti-CHIKV activity. The virucidal assay indicated that the compound does not exert a direct effect on CHIKV particles before cell infection. RT-qPCR studies further demonstrated derivative 7 significantly reduces CHIKV replication. These findings highlight the paulownin derivative 7 as a promising and selective candidate for CHIKV treatment.</p>","PeriodicalId":17962,"journal":{"name":"Letters in Applied Microbiology","volume":" ","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Letters in Applied Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/lambio/ovaf092","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Viral infections, including arboviruses such as chikungunya, zika, dengue, and mayaro fever, remain significant global health and economic challenges, fueled by the emergence and resurgence of mosquito-borne diseases. Natural products, especially plant-derived compounds, have been crucial in drug discovery and often serve as scaffolds for synthetic drug development. This study focused on modifying paulownin, an isolated lignan, through a Click reaction to incorporate 1,2,3-triazole and quinolinic ring frameworks. The resulting derivative 7 was evaluated for its in vitro antiviral activity against Alphavirus chikungunya (CHIKV). The paulownin derivative 7 did not exhibit cytotoxicity in Vero cells and demonstrated potent activity against CHIKV, with median effective concentration value of 9.05 µM and a selectivity index exceeding 16.8. Furthermore, compound 7 outperformed positive controls, being over 46 times more active against CHIKV. Cytopathic effect assays confirmed this anti-CHIKV activity. The virucidal assay indicated that the compound does not exert a direct effect on CHIKV particles before cell infection. RT-qPCR studies further demonstrated derivative 7 significantly reduces CHIKV replication. These findings highlight the paulownin derivative 7 as a promising and selective candidate for CHIKV treatment.

泡桐碱三唑-氯喹啉衍生物:一种有前途的基孔肯雅病毒抗病毒药物。
病毒感染,包括基孔肯雅热、寨卡病毒、登革热和马雅罗热等虫媒病毒,仍然是全球卫生和经济面临的重大挑战,蚊子传播疾病的出现和死灰复燃加剧了这一挑战。天然产物,特别是植物衍生的化合物,在药物发现中起着至关重要的作用,经常作为合成药物开发的支架。本研究主要是通过Click反应对分离的木脂素泡桐素进行修饰,以加入1,2,3-三唑和喹啉环框架。对所得衍生物7体外对基孔肯雅甲病毒(CHIKV)的抗病毒活性进行了评价。泡桐素衍生物7对Vero细胞无细胞毒性,对CHIKV病毒具有较强的抗虫活性,有效浓度中位数为9.05µM,选择性指数超过16.8。此外,化合物7的抗CHIKV活性是阳性对照的46倍以上。细胞病变效应实验证实了这种抗chikv病毒的活性。杀病毒实验表明,该化合物在细胞感染前对CHIKV颗粒无直接作用。RT-qPCR研究进一步证明衍生物7显著降低了CHIKV复制。这些发现突出了泡桐素衍生物7作为治疗CHIKV的有前途和选择性的候选物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Letters in Applied Microbiology
Letters in Applied Microbiology 工程技术-生物工程与应用微生物
CiteScore
4.40
自引率
4.20%
发文量
225
审稿时长
3.3 months
期刊介绍: Journal of & Letters in Applied Microbiology are two of the flagship research journals of the Society for Applied Microbiology (SfAM). For more than 75 years they have been publishing top quality research and reviews in the broad field of applied microbiology. The journals are provided to all SfAM members as well as having a global online readership totalling more than 500,000 downloads per year in more than 200 countries. Submitting authors can expect fast decision and publication times, averaging 33 days to first decision and 34 days from acceptance to online publication. There are no page charges.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信