Repurposing Finasteride and Serotonin Reuptake Inhibitors as Novel Antimicrobials: A Dual-Action Approach to Target Bacterial and Fungal Pathogens.

Reilly Taylor, Stefani Capasso-Villanueva, Anderson Jeon, Kaitlyn Daugherty, Dominic Sandell, Leah Robinson, Hugo Castillo, Alba Chavez
{"title":"Repurposing Finasteride and Serotonin Reuptake Inhibitors as Novel Antimicrobials: A Dual-Action Approach to Target Bacterial and Fungal Pathogens.","authors":"Reilly Taylor, Stefani Capasso-Villanueva, Anderson Jeon, Kaitlyn Daugherty, Dominic Sandell, Leah Robinson, Hugo Castillo, Alba Chavez","doi":"10.31083/FBE44075","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The global rise of antimicrobial resistance necessitates the development of innovative therapeutic strategies beyond traditional antibiotics. Drug repurposing offers a time- and cost-effective approach by identifying new antimicrobial applications for existing medications. Thus, this study aimed to investigate the antimicrobial and anti-virulence potential of several clinically approved drugs, including fluconazole, buspirone, duloxetine, escitalopram, and finasteride.</p><p><strong>Methods: </strong>We evaluated the antimicrobial efficacy of the selected compounds against a panel of microorganisms comprising two Gram-negative bacteria (<i>Escherichia coli</i>, <i>Serratia marcescens</i>), two Gram-positive bacteria (<i>Bacillus megaterium</i>, <i>Staphylococcus epidermidis</i>), and two opportunistic yeasts (<i>Candida albicans</i>, <i>Rhodotorula mucilaginosa</i>). Antimicrobial activity was evaluated using growth inhibition and viability assays. Additionally, we investigated the effects of the selected drugs on fungal virulence traits, including biofilm formation and filamentation, and assessed infectivity using a <i>Caenorhabditis elegans</i> host model.</p><p><strong>Results: </strong>Duloxetine and escitalopram demonstrated broad-spectrum antimicrobial activity, inhibiting bacterial and fungal growth at concentrations below 512 mg/L. Buspirone exhibited selective antimicrobial effects, particularly against Gram-positive bacteria and <i>C. albicans</i>. Although finasteride exhibited limited direct antifungal activity, it significantly disrupted key virulence traits in yeasts, including biofilm formation, morphological transitions, and host infection capacity.</p><p><strong>Conclusion: </strong>These findings underscore the potential of serotonin reuptake inhibitors and finasteride as candidates for antimicrobial repurposing. By impairing both microbial viability and pathogenicity, these drugs may provide promising avenues for developing adjunct or alternative therapies against resistant bacterial and fungal pathogens.</p>","PeriodicalId":73068,"journal":{"name":"Frontiers in bioscience (Elite edition)","volume":"18 1","pages":"44075"},"PeriodicalIF":0.0000,"publicationDate":"2026-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in bioscience (Elite edition)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31083/FBE44075","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The global rise of antimicrobial resistance necessitates the development of innovative therapeutic strategies beyond traditional antibiotics. Drug repurposing offers a time- and cost-effective approach by identifying new antimicrobial applications for existing medications. Thus, this study aimed to investigate the antimicrobial and anti-virulence potential of several clinically approved drugs, including fluconazole, buspirone, duloxetine, escitalopram, and finasteride.

Methods: We evaluated the antimicrobial efficacy of the selected compounds against a panel of microorganisms comprising two Gram-negative bacteria (Escherichia coli, Serratia marcescens), two Gram-positive bacteria (Bacillus megaterium, Staphylococcus epidermidis), and two opportunistic yeasts (Candida albicans, Rhodotorula mucilaginosa). Antimicrobial activity was evaluated using growth inhibition and viability assays. Additionally, we investigated the effects of the selected drugs on fungal virulence traits, including biofilm formation and filamentation, and assessed infectivity using a Caenorhabditis elegans host model.

Results: Duloxetine and escitalopram demonstrated broad-spectrum antimicrobial activity, inhibiting bacterial and fungal growth at concentrations below 512 mg/L. Buspirone exhibited selective antimicrobial effects, particularly against Gram-positive bacteria and C. albicans. Although finasteride exhibited limited direct antifungal activity, it significantly disrupted key virulence traits in yeasts, including biofilm formation, morphological transitions, and host infection capacity.

Conclusion: These findings underscore the potential of serotonin reuptake inhibitors and finasteride as candidates for antimicrobial repurposing. By impairing both microbial viability and pathogenicity, these drugs may provide promising avenues for developing adjunct or alternative therapies against resistant bacterial and fungal pathogens.

重新利用非那雄胺和5 -羟色胺再摄取抑制剂作为新型抗菌剂:一种针对细菌和真菌病原体的双重作用方法。
背景:全球抗菌素耐药性的上升需要发展超越传统抗生素的创新治疗策略。通过确定现有药物的新的抗菌应用,药物再利用提供了一种时间和成本效益的方法。因此,本研究旨在探讨几种临床批准的药物的抗菌和抗毒潜力,包括氟康唑、丁螺环酮、度洛西汀、艾司西酞普兰和非那雄胺。方法:我们评估了所选化合物对一组微生物的抗菌效果,这些微生物包括两种革兰氏阴性菌(大肠杆菌、粘质沙雷氏菌)、两种革兰氏阳性菌(巨芽孢杆菌、表皮葡萄球菌)和两种机会酵母菌(白色念珠菌、粘液红酵母)。通过生长抑制和活力测定来评价抗菌活性。此外,我们研究了所选药物对真菌毒力特性的影响,包括生物膜的形成和丝化,并使用秀丽隐杆线虫宿主模型评估了感染性。结果:在浓度低于512 mg/L时,度洛西汀和艾司西酞普兰具有广谱抗菌活性,抑制细菌和真菌生长。丁螺环酮表现出选择性抗菌作用,特别是对革兰氏阳性菌和白色念珠菌。尽管非那雄胺表现出有限的直接抗真菌活性,但它显著破坏了酵母的关键毒力特征,包括生物膜形成、形态转变和宿主感染能力。结论:这些发现强调了5 -羟色胺再摄取抑制剂和非那雄胺作为抗菌药物再利用的候选药物的潜力。通过削弱微生物活力和致病性,这些药物可能为开发针对耐药细菌和真菌病原体的辅助或替代疗法提供了有希望的途径。
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
自引率
0.00%
发文量
0
×
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
小红书