薄荷提取物对临床分离鲍曼不动杆菌生物膜形成抑制作用的研究。

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Iranian Journal of Pharmaceutical Research Pub Date : 2025-06-29 eCollection Date: 2025-01-01 DOI:10.5812/ijpr-160772
Zahra Majidi Fard, Negin Irani Mavi, Shokoofeh Akbari, Yousef Erfani, Sanaz Eghtedari
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引用次数: 0

摘要

背景:鲍曼不动杆菌是一种医院获得性条件致病菌,其多药耐药过程中生物膜的形成起着至关重要的作用。鉴于抗生素耐药性的上升,草药,包括薄荷(Mentha piperita),因其潜在的抗菌特性而受到关注。目的:研究薄荷提取物对鲍曼不动杆菌临床分离株生物膜形成的抑制作用。方法:从德黑兰联合医学学院临床标本中分离25株鲍曼不动杆菌。采用纸片扩散法测定其生物膜形成能力及对9种抗生素的药敏。采用孔扩散法测定薄荷提取物的抑菌活性,并与环丙沙星比较其最小抑菌浓度(MIC)和最小杀菌浓度(MBC)。分析了提取物与环丙沙星之间的协同作用,然后进行了时效试验。采用聚合酶链反应(PCR)检测与生物膜形成相关的PgaA和AbaI基因的存在。结果:研究发现88%的鲍曼不动杆菌菌株表现出较强的生物膜形成。薄荷提取物能有效抑制生物膜的形成,其MIC值为1.5 ~ 6 mg/mL(平均MIC为3.75±1.38 mg/mL), MBC值与其MIC浓度相当。对于环丙沙星,所有样品的MIC均大于2048 mg/mL。薄荷提取物与环丙沙星之间没有明显的协同作用。PgaA(参与生物膜基质合成)和AbaI(群体感应相关的自诱导剂合成酶)基因均存在于所有测试菌株中。结论:薄荷提取物显示出对鲍曼不动杆菌的生物膜抑制特性,表明其有潜力作为对抗生物膜相关感染的替代治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Investigation of Peppermint (<i>Mentha piperita</i>) Extract on the Inhibition of Biofilm Formation by <i>Acinetobacter baumannii</i> Strains Isolated from Clinical Samples.

Investigation of Peppermint (<i>Mentha piperita</i>) Extract on the Inhibition of Biofilm Formation by <i>Acinetobacter baumannii</i> Strains Isolated from Clinical Samples.

Investigation of Peppermint (Mentha piperita) Extract on the Inhibition of Biofilm Formation by Acinetobacter baumannii Strains Isolated from Clinical Samples.

Background: Acinetobacter baumannii is a hospital-acquired opportunistic pathogen, with biofilm formation playing a crucial role in its multidrug resistance. Given the rise in antibiotic resistance, herbal medicines, including peppermint (Mentha piperita), have gained attention for their potential antibacterial properties.

Objectives: This study aimed to evaluate the inhibitory effects of peppermint extract on biofilm formation in A. baumannii strains isolated from clinical samples.

Methods: A total of 25 A. baumannii strains were isolated from clinical samples at the Faculty of Allied Medical Sciences, Tehran. Their biofilm-forming ability and antibiotic susceptibility against nine antibiotics were assessed using the disk diffusion method. The antibacterial activity of peppermint extract was evaluated by well diffusion, with its minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) compared to ciprofloxacin. Synergistic effects between the extract and ciprofloxacin were analyzed, followed by a time-kill assay. Polymerase chain reaction (PCR) was used to detect the presence of PgaA and AbaI genes linked to biofilm formation.

Results: The study found that 88% of A. baumannii strains exhibited strong biofilm formation. Peppermint extract effectively inhibited biofilm formation, with MIC values ranging from 1.5 to 6 mg/mL (mean MIC: 3.75 ± 1.38 mg/mL) and MBC values equivalent to their respective MIC concentrations. For ciprofloxacin, the MIC for all samples was greater than 2048 mg/mL. No significant synergistic effect was observed between peppermint extract and ciprofloxacin. Both PgaA (involved in biofilm matrix synthesis) and AbaI (quorum sensing-related autoinducer synthase) genes were present in all tested strains.

Conclusions: Peppermint extract demonstrates biofilm-inhibitory properties against A. baumannii, suggesting its potential as an alternative therapeutic approach for combating biofilm-associated infections.

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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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