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莫尔登克氏木(Moldenke)提取物的植物化学成分、抗菌及抗生素抗性调节活性,劳森氏木(Lawson)及L. 对多重耐药菌的作用

Phytochemical Composition, Antibacterial, and Antibiotic-Resistance Modulatory Activity of Extracts of Moldenke M. A. Lawson, and L. Against Multidrug-Resistant .

作者信息

Mouozong Richard, Fankam Aimé Gabriel, Diffo Varelle Lambou, Matieta Valaire Yemene, Megaptche Fabrice Junior, Kuete Victor

机构信息

Department of Biochemistry, University of Dschang, Dschang, Cameroon.

出版信息

Scientifica (Cairo). 2024 Dec 24;2024:3403280. doi: 10.1155/sci5/3403280. eCollection 2024.

Abstract

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 and extracts alone and in combination with antibiotics against multidrug-resistant (MDR) . 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 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. leaf extract demonstrated the highest phenolic content (151.59 mg GAE/g), while 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, leaf extract (MIC/8), although weakly active, had improved by 2 to 64-fold the activity of imipenem, streptomycin, kanamycin, and ceftriaxone against MDR . It also showed synergy (ΣFIC ≤ 0.5) with streptomycin, ampicillin, tetracycline, and vancomycin against PA3. The overall results indicate that the tested extracts, especially those from and leaves, necessitate further exploration for the development of natural drugs to treat infections caused by MDR .

摘要

是一种关键级别的病原体,对大多数传统抗生素具有很强的抗性。因此,寻找新型药物来对抗这种细菌引起的感染至关重要。本研究旨在评估单独以及与抗生素联合使用时,[提取物名称]和[提取物名称]提取物对多重耐药(MDR)[细菌名称]的抗菌活性。使用标准的定性和定量分析方法进行植物化学分析。采用微量稀释法评估提取物的抗菌和抗生素抗性调节活性。使用棋盘肉汤微量稀释法研究抗生素与[植物名称]叶提取物之间的相互作用。在所有提取物中均检测到酚类和黄酮类物质,而其他植物化学类别则选择性分布。[植物名称]叶提取物显示出最高的酚类含量(151.59 mg GAE/g),而[植物名称]叶(LML)提取物显示出最高的黄酮类含量(24.51 mg QE/g)。这些提取物表现出抗菌活性,最低抑菌浓度(MIC)范围为128至2048 μg/mL。LML提取物表现出最佳的抗假单胞菌活性,对ATCC 27853的MIC为128 μg/mL,对一些MDR分离株(PA1、PA2和PA7)的MIC为256 μg/mL。此外,[植物名称]叶提取物(MIC/8)虽然活性较弱,但使亚胺培南、链霉素、卡那霉素和头孢曲松对MDR [细菌名称]的活性提高了2至64倍。它还与链霉素、氨苄西林、四环素和万古霉素对[细菌名称]PA3表现出协同作用(ΣFIC≤0.5)。总体结果表明,所测试的提取物,特别是来自[植物名称]和[植物名称]叶的提取物,有必要进一步探索以开发用于治疗MDR [细菌名称]引起的感染的天然药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/11688135/18f7eb7e06d2/SCIENTIFICA2024-3403280.001.jpg

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