Javadi Kasra, Ahmadi Mohammad Hossein, Rajabnia Mehdi, Halaji Mehrdad
Department of Microbiology, Faculty of Medicine, Shahed University, Tehran, Iran.
Infectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
Int J Mol Cell Med. 2025;14(1):567-575. doi: 10.22088/IJMCM.BUMS.14.1.567.
Multi-drug-resistant (MDR) has become a major global healthcare concern due to its opportunistic infections and high antibiotic resistance. This investigation is intended to investigate curcumin's potential anti-bacterial and antibiofilm impacts on MDR . and to present a promising strategy for fighting against infections caused by this pathogen. This cross-sectional investigation comprised 34 MDR . clinical isolates. The Kirby-Bauer disc diffusion method evaluated the sensitivity of isolates to multifaceted anti-bacterial agents. The microdilution broth method quantified curcumin's minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC). The efficacy of curcumin in inhibiting MDR . biofilm was assessed via 96-well microtiter plates. The expression of the biofilm-associated protein () gene was evaluated by employing quantitative real-time PCR (qRT-PCR). Within the 34 MDR . isolates, the highest resistance was noted for trimethoprim/sulfamethoxazole and ciprofloxacin, with all 34 isolates (100%) indicating resistance. The lowest resistance was noted for ampicillin/sulbactam, with 22 isolates (64.7%) exhibiting resistance. The MICs of curcumin ranged from 0.625 to 2.5 mg/ml, while the MBCs varied between 1.25 to 5 mg/ml. Curcumin reduced biofilm formation by 25% to 91%, depending on the concentration. In contrast to the untreated control, the average relative activity of the gene in MDR isolates declined by 62.07%. The findings indicate that curcumin demonstrates antimicrobial and anti-biofilm activities against MDR . . The downregulation noted in the gene further supports the curcumin's anti-biofilm impact.
多重耐药(MDR)因其机会性感染和高抗生素耐药性已成为全球主要的医疗保健问题。本研究旨在调查姜黄素对MDR的潜在抗菌和抗生物膜影响,并提出一种对抗由该病原体引起的感染的有前景的策略。这项横断面研究包括34株MDR临床分离株。Kirby-Bauer纸片扩散法评估了分离株对多种抗菌剂的敏感性。微量稀释肉汤法测定了姜黄素的最低抑菌浓度(MIC)和最低杀菌浓度(MBC)。通过96孔微量滴定板评估姜黄素抑制MDR生物膜的效果。采用定量实时PCR(qRT-PCR)评估生物膜相关蛋白()基因的表达。在34株MDR分离株中,对甲氧苄啶/磺胺甲恶唑和环丙沙星的耐药性最高,所有34株分离株(100%)均显示耐药。对氨苄西林/舒巴坦的耐药性最低,22株分离株(64.7%)表现出耐药。姜黄素的MIC范围为0.625至2.5mg/ml,而MBC在1.25至5mg/ml之间变化。姜黄素根据浓度将生物膜形成减少了25%至91%。与未处理的对照相比,MDR分离株中该基因的平均相对活性下降了62.07%。研究结果表明,姜黄素对MDR表现出抗菌和抗生物膜活性。该基因的下调进一步支持了姜黄素的抗生物膜作用。