Activity of Fluoroquinolones and Proton Pump Inhibitors against Resistant Oral Bacterial Biofilms, in silico and in vitro Analysis.

Polish journal of microbiology Pub Date : 2024-09-13 eCollection Date: 2024-09-01 DOI:10.33073/pjm-2024-028
Muhammad Kamran, Muhammad Raza, Riaz Ullah, Amal Alotaibi, Ràheela Bano, Ali Zaman, Sadia Chaman, Kashif Iqbal, Shahid Rasool, Adnan Amin
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Abstract

Oral bacterial infections are a great health concern worldwide especially in diabetic patients. Emergence of antimicrobial resistance with reference to biofilms in oral cavity is of great concern. We investigated antibiotics combination with proton pump inhibitors against oral clinical isolates. The strains were identified as Staphylococcus epidermidis and Staphylococcus aureus by the 16S rRNA gene sequencing. In molecular docking, ciprofloxacin, levofloxacin, and omeprazole best fit to active pockets of transcriptional regulators 4BXI and 3QP1. None of the proton pump inhibitors were active against S. epidermidis, whereas omeprazole showed significant inhibition (MIC 3.9 μg/ml). Fluoroquinolones were active against both S. epidermidis and S. aureus. In combination analysis, a marked decrease in minimum inhibitory concentration was noticed with omeprazole (MIC 0.12 μg/ml). In antiquorum sensing experiments, a significant inhibitory zone was shown for all fluoroquinolones (14-20 mm), whereas among proton pump inhibitors, only omeprazole (12 ± 0.12 mm) was active against Chromobacterium violaceum. In combination analysis, a moderate increase in antiquorum sensing activity was recorded for ciprofloxacin, ofloxacin, and proton pump inhibitors. Further, significant S. aureus biofilm eradication was recorded using of ciprofloxacin, levofloxacin, and omeprazole combination (78 ± 2.1%). The time-kill kinetic studies indicated a bactericidal effect by ciprofloxacin: levofloxacin: omeprazole combination over 24 hrs. It was concluded that fluoroquinolone combined with omeprazole could be an effective treatment option for eradicating oral bacterial biofilms.

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氟喹诺酮类药物和质子泵抑制剂对耐药口腔细菌生物膜的活性,硅学和体外分析。
口腔细菌感染是全球关注的一大健康问题,尤其是糖尿病患者。口腔中生物膜产生的抗菌药耐药性令人十分担忧。我们研究了抗生素与质子泵抑制剂对口腔临床分离菌株的联合作用。通过 16S rRNA 基因测序,确定这些菌株为表皮葡萄球菌和金黄色葡萄球菌。在分子对接中,环丙沙星、左氧氟沙星和奥美拉唑最适合转录调节剂 4BXI 和 3QP1 的活性袋。没有一种质子泵抑制剂对表皮葡萄球菌具有活性,而奥美拉唑具有显著的抑制作用(MIC 3.9 μg/ml)。氟喹诺酮类药物对表皮葡萄球菌和金黄色葡萄球菌均有效。在联合分析中,发现奥美拉唑的最小抑菌浓度明显下降(MIC 0.12 μg/ml)。在抗喹诺酮感应实验中,所有氟喹诺酮类药物都显示出明显的抑制区(14-20 毫米),而在质子泵抑制剂中,只有奥美拉唑(12 ± 0.12 毫米)对暴力色杆菌具有活性。在联合分析中,环丙沙星、氧氟沙星和质子泵抑制剂的抗菌传感活性都有适度的增加。此外,环丙沙星、左氧氟沙星和奥美拉唑的组合能明显消除金黄色葡萄球菌的生物膜(78 ± 2.1%)。时间杀灭动力学研究表明,环丙沙星:左氧氟沙星:奥美拉唑复方制剂在 24 小时内具有杀菌作用。结论是氟喹诺酮类药物与奥美拉唑联用可作为根除口腔细菌生物膜的有效治疗方案。
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