Phytochemical Composition, Antibacterial, and Antibiotic-Resistance Modulatory Activity of Extracts of Lippia multiflora Moldenke, Terminalia mollis M. A. Lawson, and Cinchona officinalis L. Against Multidrug-Resistant Pseudomonas aeruginosa.

IF 2.3 Q2 BIOLOGY
Scientifica Pub Date : 2024-12-24 eCollection Date: 2024-01-01 DOI:10.1155/sci5/3403280
Richard Mouozong, Aimé Gabriel Fankam, Varelle Lambou Diffo, Valaire Yemene Matieta, Fabrice Junior Megaptche, Victor Kuete
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引用次数: 0

Abstract

Pseudomonas aeruginosa is a critical-class pathogen that shows great resistance to most conventional antibiotics. Hence, it is of utmost importance to search for novel drugs to fight infections caused by this bacterium. This study aimed to evaluate the antibacterial activity of Lippia multiflora, Terminalia mollis, and Cinchona officinalis extracts alone and in combination with antibiotics against multidrug-resistant (MDR) P. aeruginosa. Phytochemical analysis was performed using standard qualitative and quantitative assays. The microdilution method was used to assess the antibacterial and antibiotic-resistance modulatory activity of the extracts. The interaction between antibiotics and Cinchona officinalis leaf extract was carried out using the checkerboard broth microdilution method. Phenols and flavonoids were detected in all extracts, whereas other phytochemical classes were selectively distributed. T. mollis leaf extract demonstrated the highest phenolic content (151.59 mg GAE/g), while L. multiflora leaf (LML) extract showed the highest flavonoid content (24.51 mg QE/g). These extracts exhibited antibacterial activity, with minimum inhibitory concentrations (MICs) ranging from 128 to 2048 μg/mL. LML extract displayed the best antipseudomonal activity, with MIC of 128 μg/mL against ATCC 27853 and 256 μg/mL against some MDR isolates (PA1, PA2, and PA7). Moreover, C. officinalis leaf extract (MIC/8), although weakly active, had improved by 2 to 64-fold the activity of imipenem, streptomycin, kanamycin, and ceftriaxone against MDR P. aeruginosa. It also showed synergy (ΣFIC ≤ 0.5) with streptomycin, ampicillin, tetracycline, and vancomycin against P. aeruginosa PA3. The overall results indicate that the tested extracts, especially those from L. multiflora and C. officinalis leaves, necessitate further exploration for the development of natural drugs to treat infections caused by MDR P. aeruginosa.

多花Lippia Moldenke, Terminalia mollis M. A. Lawson和金鸡纳officinalis L.提取物对多重耐药铜绿假单胞菌的植物化学成分、抗菌和耐药调节活性。
铜绿假单胞菌是一种对大多数常规抗生素具有很强耐药性的临界类病原体。因此,寻找新的药物来对抗这种细菌引起的感染是至关重要的。本研究旨在评价多花Lippia、Terminalia mollis和金鸡纳提取物单独及联合抗生素对多重耐药(MDR)铜绿假单胞菌(P. aeruginosa)的抗菌活性。采用标准的定性和定量方法进行植物化学分析。采用微量稀释法评价提取物的抑菌和耐药调节活性。采用棋盘肉汤微量稀释法研究抗生素与金鸡纳叶提取物的相互作用。在所有提取物中均检测到酚类和黄酮类,而其他植物化学类则选择性分布。黄酮含量最高的是白羊草叶提取物(24.51 mg QE/g),黄酮含量最高的是白羊草叶提取物(151.59 mg QE/g)。这些提取物具有抗菌活性,最低抑菌浓度(mic)为128 ~ 2048 μg/mL。LML提取物对ATCC 27853的MIC值为128 μg/mL,对部分MDR菌株(PA1、PA2和PA7)的MIC值为256 μg/mL。此外,山茱萸叶提取物(MIC/8)虽然活性较弱,但对耐多药铜绿假单胞菌的亚胺培南、链霉素、卡那霉素和头孢曲松的活性提高了2 ~ 64倍。与链霉素、氨苄西林、四环素、万古霉素对铜绿假单胞菌PA3有协同作用(ΣFIC≤0.5)。综上所述,这些提取物,尤其是多花假单胞菌和officinalis叶片提取物,值得进一步探索开发治疗耐多药铜绿假单胞菌感染的天然药物。
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来源期刊
Scientifica
Scientifica BIOLOGY-
CiteScore
6.70
自引率
0.00%
发文量
43
审稿时长
21 weeks
期刊介绍: Scientifica is a peer-reviewed, Open Access journal that publishes research articles, review articles, and clinical studies covering a wide range of subjects in the life sciences, environmental sciences, health sciences, and medicine. The journal is divided into the 65 subject areas.
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