{"title":"Attenuation of Type IV pili activity by natural products.","authors":"Kerem Yalkut, Soumaya Ben Ali Hassine, Esra Basaran, Ceyda Kula, Aslıhan Ozcan, Fatma Gizem Avci, Ozlem Keskin, Berna Sariyar Akbulut, Pemra Ozbek","doi":"10.1080/07391102.2024.2310781","DOIUrl":null,"url":null,"abstract":"<p><p>The virulence factor Type IV pili (T4P) are surface appendages used by the opportunistic pathogen <i>Pseudomonas aeruginosa</i> for twitching motility and adhesion in the environment and during infection. Additionally, the use of these appendages by <i>P. aeruginosa</i> for biofilm formation increases its virulence and drug resistance. Therefore, attenuation of the activity of T4P would be desirable to control <i>P. aeruginosa</i> infections. Here, a computational approach has been pursued to screen natural products that can be used for this purpose. PilB, the elongation ATPase of the T4P machinery in <i>P. aeruginosa</i>, has been selected as the target subunit and virtual screening of FDA-approved drugs has been conducted. Screening identified two natural compounds, ergoloid and irinotecan, as potential candidates for inhibiting this T4P-associated ATPase in <i>P. aeruginosa</i>. These candidate compounds underwent further rigorous evaluation through molecular dynamics (MD) simulations and then through <i>in vitro</i> twitching motility and biofilm inhibition assays. Notably, ergoloid emerged as a particularly promising candidate for weakening the T4P activity by inhibiting the elongation ATPases associated with T4P. This repurposing study paves the way for the timely discovery of antivirulence drugs as an alternative to classical antibiotic treatments to help combat infections caused by <i>P. aeruginosa</i> and related pathogens.</p>","PeriodicalId":15272,"journal":{"name":"Journal of Biomolecular Structure & Dynamics","volume":" ","pages":"5719-5729"},"PeriodicalIF":2.4000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biomolecular Structure & Dynamics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1080/07391102.2024.2310781","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/2/2 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The virulence factor Type IV pili (T4P) are surface appendages used by the opportunistic pathogen Pseudomonas aeruginosa for twitching motility and adhesion in the environment and during infection. Additionally, the use of these appendages by P. aeruginosa for biofilm formation increases its virulence and drug resistance. Therefore, attenuation of the activity of T4P would be desirable to control P. aeruginosa infections. Here, a computational approach has been pursued to screen natural products that can be used for this purpose. PilB, the elongation ATPase of the T4P machinery in P. aeruginosa, has been selected as the target subunit and virtual screening of FDA-approved drugs has been conducted. Screening identified two natural compounds, ergoloid and irinotecan, as potential candidates for inhibiting this T4P-associated ATPase in P. aeruginosa. These candidate compounds underwent further rigorous evaluation through molecular dynamics (MD) simulations and then through in vitro twitching motility and biofilm inhibition assays. Notably, ergoloid emerged as a particularly promising candidate for weakening the T4P activity by inhibiting the elongation ATPases associated with T4P. This repurposing study paves the way for the timely discovery of antivirulence drugs as an alternative to classical antibiotic treatments to help combat infections caused by P. aeruginosa and related pathogens.
致病因子 IV 型纤毛(T4P)是机会性病原体铜绿假单胞菌用于在环境中和感染期间抽动运动和粘附的表面附属物。此外,铜绿假单胞菌利用这些附属物形成生物膜,增加了其毒性和耐药性。因此,减弱 T4P 的活性是控制铜绿假单胞菌感染的理想方法。在此,我们采用一种计算方法来筛选可用于这一目的的天然产物。PilB 是铜绿假单胞菌 T4P 机制的延伸 ATP 酶,已被选为目标亚基,并对 FDA 批准的药物进行了虚拟筛选。筛选确定了两种天然化合物--麦角酮和伊立替康--作为抑制铜绿假单胞菌 T4P 相关 ATP 酶的潜在候选化合物。通过分子动力学(MD)模拟,然后通过体外抽动运动和生物膜抑制试验,对这些候选化合物进行了进一步的严格评估。值得注意的是,ergoloid 通过抑制与 T4P 相关的伸长 ATP 酶,成为一种特别有希望削弱 T4P 活性的候选化合物。这项再利用研究为及时发现抗病毒药物铺平了道路,这些药物可替代传统的抗生素治疗,帮助对抗铜绿假单胞菌和相关病原体引起的感染。
期刊介绍:
The Journal of Biomolecular Structure and Dynamics welcomes manuscripts on biological structure, dynamics, interactions and expression. The Journal is one of the leading publications in high end computational science, atomic structural biology, bioinformatics, virtual drug design, genomics and biological networks.