Exploring the Antibacterial Potential of Bile Salts: Inhibition of Biofilm Formation and Cell Growth in Pseudomonas aeruginosa and Staphylococcus aureus

Anuradha Tyagi, Vinay Kumar, Navneet Joshi, H. Dhingra
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Abstract

Chronic infections often involve notorious pathogens like Pseudomonas aeruginosa and Staphylococcus aureus, demanding innovative antimicrobial strategies due to escalating resistance. This investigation scrutinized the antibacterial prowess of bile salts, notably taurocholic acid (TCA), ursodeoxycholic acid (UDCA), and ox bile salt (OBS), against these pathogens. Evaluations encompassed minimum inhibitory concentration (MIC) determination, scrutiny of their impact on biofilm formation, and anti-virulence mechanisms. UDCA exhibited the highest efficacy, suppressing S. aureus and P. aeruginosa biofilms by 83.5% and 78%, respectively, at peak concentration. TCA also significantly reduced biofilm development by 81% for S. aureus and 75% for P. aeruginosa. Microscopic analysis revealed substantial disruption of biofilm architecture by UDCA and TCA. Conversely, OBS demonstrated ineffectiveness against both pathogens. Mechanistic assays elucidated UDCA and TCA’s detrimental impact on the cell membrane, prompting the release of macromolecular compounds. Additionally, UDCA and TCA inhibited protease and elastase synthesis in P. aeruginosa and staphyloxanthin and lipase production in S. aureus. These results underscore the potential of UDCA and TCA in impeding biofilm formation and mitigating the pathogenicity of S. aureus and P. aeruginosa.
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探索胆盐的抗菌潜力:抑制铜绿假单胞菌和金黄色葡萄球菌的生物膜形成和细胞生长
慢性感染通常涉及绿脓杆菌和金黄色葡萄球菌等臭名昭著的病原体,由于耐药性不断升级,需要创新的抗菌策略。本研究仔细研究了胆盐(主要是牛胆酸(TCA)、熊去氧胆酸(UDCA)和牛胆盐(OBS))对这些病原体的抗菌能力。评估包括最低抑菌浓度(MIC)测定、对生物膜形成的影响以及抗病毒机制的研究。UDCA 的疗效最高,在峰值浓度下对金黄色葡萄球菌和铜绿假单胞菌生物膜的抑制率分别为 83.5% 和 78%。三氯乙酸也能明显减少生物膜的形成,对金黄色葡萄球菌的抑制率为 81%,对铜绿假单胞菌的抑制率为 75%。显微镜分析表明,UDCA 和 TCA 能极大地破坏生物膜结构。相反,OBS 则对这两种病原体无效。机理测定阐明了 UDCA 和 TCA 对细胞膜的有害影响,促使大分子化合物的释放。此外,UDCA 和 TCA 还可抑制铜绿假单胞菌蛋白酶和弹性蛋白酶的合成,以及金黄色葡萄球菌钉螺黄素和脂肪酶的产生。这些结果强调了 UDCA 和 TCA 在阻碍生物膜形成和减轻金黄色葡萄球菌和铜绿假单胞菌致病性方面的潜力。
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