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靶向口腔细菌病原体的生物活性植物废料成分作为根除生物膜的一种有前景的策略。

Bioactive plant waste components targeting oral bacterial pathogens as a promising strategy for biofilm eradication.

作者信息

Mashal Saima, Siddiqua Aisha, Ullah Niamat, Baloch Rabia, Khan Momin, Hasnain Syed Zia Ul, Imran Aziz Muhammad, Huseynov Elchin, Selakovic Dragica, Rosic Gvozden, Makhkamov Trobjon, Yuldashev Akramjon, Islamov Sokhib, Abdullayeva Nilufar, Khujanazarov Uktam, Amin Adnan

机构信息

Gomal Center of Biochemistry and Biotechnology (GCBB), Gomal University, Dera Ismail Khan, Khyber Pakhtunkhwa, Pakistan.

Natural Products Research Lab, Department of Pharmacognosy, Faculty of Pharmacy, Gomal University, Dera Ismail Khan, Khyber Pakhtunkhwa, Pakistan.

出版信息

Front Chem. 2024 Aug 9;12:1406869. doi: 10.3389/fchem.2024.1406869. eCollection 2024.

DOI:10.3389/fchem.2024.1406869
PMID:39185371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11341444/
Abstract

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 and 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 , , , and . 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 , , and . 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 ), cinnamic acid (80.9% ± 1.1% inhibition against ), and vanillic acid and quercetin (65.5% ± 1.7% and 87.4% ± 1.4% inhibition, respectively, against ) 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.

摘要

本研究的意义在于探索生物活性植物提取物,将其作为对抗口腔细菌病原体的一条有前景的途径,为生物膜根除提供了一种新策略,这可能会彻底改变口腔健康治疗方法。口腔细菌感染在糖尿病患者中很常见;然而,由于耐药性的产生,治疗选择有限。考虑到酚类化合物具有出色的抗菌特性,我们使用 和 模型研究了它们对分离出的口腔病原体的作用。我们进行了抗菌谱研究以及涵盖酚类化合物的最低抑菌浓度(MIC)、抗生物膜和群体感应抑制活性研究。从女性糖尿病患者中分离出细菌菌株,并通过16S rRNA测序鉴定为 、 、 和 。抗菌谱研究证实,除亚胺培南和环丙沙星外,所有菌株对大多数测试抗生素均耐药。分子对接分析显示,芦丁、槲皮素、没食子酸和儿茶素与转录调节基因 、 和 有显著相互作用。除芦丁外,所有测试分子均符合类药规则。测试化合物对临床分离株的MIC值在0.0625至0.5 mg/mL之间。儿茶素(对 抑制率为73.5% ± 1.6%)、肉桂酸(对 抑制率为80.9% ± 1.1%)、香草酸和槲皮素(对 抑制率分别为65.5% ± 1.7%和87.4% ± 1.4%)在0.25 - 0.125 mg/mL时具有显著的抗生物膜活性。酚类化合物均未表现出群体感应抑制活性。因此,得出结论,多酚类化合物可能有潜力用于对抗口腔细菌生物膜,应进一步进行详细的作用机制研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/b3783cfe8461/fchem-12-1406869-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/5262366437c4/fchem-12-1406869-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/6e22a4d37f2e/fchem-12-1406869-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/bf7f6ebfaf42/fchem-12-1406869-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/458a325c3073/fchem-12-1406869-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/78040a19d8ed/fchem-12-1406869-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/b3783cfe8461/fchem-12-1406869-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/5262366437c4/fchem-12-1406869-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/6e22a4d37f2e/fchem-12-1406869-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/bf7f6ebfaf42/fchem-12-1406869-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/458a325c3073/fchem-12-1406869-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/78040a19d8ed/fchem-12-1406869-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/11341444/b3783cfe8461/fchem-12-1406869-g006.jpg

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