针对口腔细菌病原体的植物废弃物生物活性成分是消除生物膜的有效策略

Saima Mashal, Aisha Siddiqua, Niamat Ullah, R. Baloch, Momin Khan, Syed Zia ul Hasnain, Muhammad Imran Aziz, Elchin Huseynov, D. Selaković, G. Rosic, T. Makhkamov, A. Yuldashev, S. Islamov, Nilufar Abdullayeva, Uktam Khujanazarov, Adnan Amin
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摘要

这项研究的意义在于探索了生物活性植物萃取物这一抗击口腔细菌病原体的有效途径,为消除生物膜提供了一种新策略,有可能彻底改变口腔健康治疗方法。口腔细菌感染是糖尿病患者的常见病;然而,由于耐药性的产生,治疗方案十分有限。考虑到酚类化合物具有出色的抗菌特性,我们利用硅学和体外模型研究了它们对分离的口腔病原体的作用。我们对酚类化合物进行了抗菌谱研究以及最低抑菌浓度(MIC)、抗生物膜和抗阙值感应活性研究。细菌菌株从女性糖尿病患者体内分离出来,通过 16S rRNA 测序鉴定为铜绿假单胞菌、中港芽孢杆菌、副黏液芽孢杆菌和树枝状芽孢杆菌。抗生素图谱研究证实,除亚胺培南和环丙沙星外,所有菌株都对大多数测试抗生素具有耐药性。分子对接分析表明,芦丁、槲皮素、没食子酸和儿茶素与转录调节基因 1RO5、4B2O 和 5OE3 有明显的相互作用。除芦丁外,所有受试分子都遵循药物相似性规则。测试化合物对临床分离菌的 MIC 值从 0.0625 到 0.5 mg/mL 不等。在 0.25-0.125 毫克/毫升的浓度下,儿茶素(对巴氏杆菌的抑制率为 73.5% ± 1.6%)、肉桂酸(对铜绿假单胞菌的抑制率为 80.9% ± 1.1%)、香草酸和槲皮素(对 B. chungangensis 的抑制率分别为 65.5% ± 1.7% 和 87.4% ± 1.4%)具有显著的抗生物膜活性。没有一种酚类化合物具有抗虫感应活性。因此,结论是多酚类化合物可能具有用于抑制口腔细菌生物膜的潜力,应进一步进行详细的机理研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioactive plant waste components targeting oral bacterial pathogens as a promising strategy for biofilm eradication
The significance of this study lies in its exploration of bioactive plant extracts as a promising avenue for combating oral bacterial pathogens, offering a novel strategy for biofilm eradication that could potentially revolutionize oral health treatments. Oral bacterial infections are common in diabetic patients; however, due to the development of resistance, treatment options are limited. Considering the excellent antimicrobial properties of phenolic compounds, we investigated them against isolated oral pathogens using in silico and in vitro models. We performed antibiogram studies and minimum inhibitory concentration (MIC), antibiofilm, and antiquorum sensing activities covering phenolic compounds. Bacterial strains were isolated from female diabetic patients and identified by using 16S rRNA sequencing as Pseudomonas aeruginosa, Bacillus chungangensis, Bacillus paramycoides, and Paenibacillus dendritiformis. Antibiogram studies confirmed that all strains were resistant to most tested antibiotics except imipenem and ciprofloxacin. Molecular docking analysis revealed the significant interaction of rutin, quercetin, gallic acid, and catechin with transcription regulator genes 1RO5, 4B2O, and 5OE3. All tested molecules followed drug-likeness rules except rutin. The MIC values of the tested compounds varied from 0.0625 to 0.5 mg/mL against clinical isolates. Significant antibiofilm activity was recorded in the case of catechin (73.5% ± 1.6% inhibition against B. paramycoides), cinnamic acid (80.9% ± 1.1% inhibition against P. aeruginosa), and vanillic acid and quercetin (65.5% ± 1.7% and 87.4% ± 1.4% inhibition, respectively, against B. chungangensis) at 0.25–0.125 mg/mL. None of the phenolic compounds presented antiquorum sensing activity. It was, therefore, concluded that polyphenolic compounds may have the potential to be used against oral bacterial biofilms, and further detailed mechanistic investigations should be performed.
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