Bioactive Compounds as a Potential Inhibitor of Biofilm Production: An In silico Study to Identify Natural Hindrance Resources.

Jai Gupta, Avi Gupta, Debasmita Bhattacharya, Moupriya Nag, Dibyajit Lahiri, Debanjan Mitra
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Abstract

Background: Biofilm formation by microorganisms, specifically bacteria, threatens vari-ous fields, including biomedicine and the environment. The development of biofilms has associations with increased resistance to antimicrobial agents and immune responses; it poses a significant threat to human health. ESKAPE pathogens, a group of bacteria known for their multidrug resistance, are particularly adept at biofilm formation. This research explores strategies to combat biofilm-associated infections, with a focus on natural compounds as potential anti-biofilm agents.

Methods: The study investigates 23 natural compounds for their druglike properties in fighting against antibiotic-resistant biofilms. These compounds include flavonoids, terpenes, and alkaloids, and exhibit promising bioavailability and usage potential as ligands. Molecular docking analysis em-ploying AutoDock Vina was used to evaluate the binding affinities of these ligands to key biofilm-forming genes and membrane proteins in ESKAPE pathogens.

Results: Despite a few violations of a variety of established criteria, the overall safety and efficiency of oral drug reception are maintained, emphasizing their potential for further drug development. The results show specific ligands, such as Baicalin, Apigenin, Azadirachtin, Curcumin, Hyperforin, etc., demonstrating high binding energies against biofilm-associated proteins. This approach aligns with the pursuit of sustainable alternatives to combat biofilm-related infections.

Conclusion: Natural compounds like Baicalin, Apigenin, Azadirachtin, Curcumin, Hyperforin not only exhibit broad-spectrum coverage but also show reduced risks of resistance development com-pared to synthetic antibiotics. The integration of natural compounds into multifaceted strategies con-siders the complexities of the biofilm matrix, bacterial diversity, and pathogen characteristics, offer-ing a sustainable approach to address biofilm-associated infections.

生物活性化合物作为生物膜生产的潜在抑制剂:天然屏障资源的硅研究。
背景:微生物,特别是细菌形成的生物膜威胁着包括生物医学和环境在内的各个领域。生物膜的形成与抗菌剂耐药性和免疫反应增强有关;它对人类健康构成重大威胁。ESKAPE病原体是一组以耐多药而闻名的细菌,它们特别擅长生物膜的形成。本研究探讨了对抗生物膜相关感染的策略,重点是天然化合物作为潜在的抗生物膜剂。方法:研究了23种天然化合物抗耐药生物膜的药物特性。这些化合物包括类黄酮、萜烯和生物碱,作为配体具有良好的生物利用度和使用潜力。利用AutoDock Vina进行分子对接分析,评估这些配体与ESKAPE病原菌中关键生物膜形成基因和膜蛋白的结合亲和力。结果:尽管存在一些违反各种既定标准的情况,但口服药物接受的总体安全性和有效性保持不变,强调了其进一步药物开发的潜力。结果表明,黄芩苷、芹菜素、印楝素、姜黄素、金丝桃素等配体对生物膜相关蛋白具有较高的结合能。这种方法与追求可持续的替代品来对抗生物膜相关的感染是一致的。结论:与合成抗生素相比,黄芩苷、芹菜素、印楝素、姜黄素、金丝桃素等天然化合物不仅具有广谱覆盖,而且具有较低的耐药风险。将天然化合物整合到多方面的策略中,考虑了生物膜基质的复杂性、细菌多样性和病原体特征,为解决生物膜相关感染提供了一种可持续的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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