Anti-inflammatory and Antimicrobial Potential of Three Natural Polyketides Isolated from Endophytic Fungus Phomopsis sp CAM212 against to Dysenteric Causing Pathogens

Marie Louise Medoua, Sylvain Nsangou Pechangou, B. E. Enang II, Assam Assam Jean Paul, E. Njoya, F. N. Njayou, P. Moundipa
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Abstract

Aims: The present work aimed to evaluate the anti-amoebic, antibacterial, and anti-inflammatory potential of three natural polyketides from Phomopsis sp. CAM212. Study Design: Clinical isolates of E.histolytica, E.coli ATCC25922 strain, primary peritoneal mouse macrophages and three polyketides were used. Places and Duration of Study: Laboratory of Pharmacology and Toxicology, Laboratory of Medical Microbiology, Faculty of Science, University of Yaounde 1 between May and December 2022. Methodology: During this work, we evaluated the ability of three natural polyketides from Phomopsis sp to inhibit the growth of germs responsible for amoebic and bacillary dysentery. First, the anti-amoebic activity was carried out on clinical isolates of E. histolytica in polyxenic culture. Subsequently, we evaluated the antibacterial potential on a strain of E. coli ATCC25922. Finally, the anti-inflammatory potentials were evaluated on a primary culture of SC activated macrophages through inhibition of nitric oxide (NO) production, activation of phosphatase alcaline (ALP) and inhibition of 5-lipoxygenase (5-LOX). Results: It emerges from this work that among compounds, phomopsinin B, presented the highest anti-amoebic potential (84.4 % inhibition after 72h) and the highest antibacterial potential (MIC=12.5µg/mL and MBC/MIC=2). Phomopsini A and phomopsini A acetate showed moderate anti amoebic and antibacterial potentials. However, all these activities remain lower than that of metronidazole and ciprofloxacin (90% of amoebic inhibition after 72h; MIC=0.72µg/mL and MBC/MIC=4). Subsequently, all tested compounds were nontoxic on primary macrophages. Phomopsinin B exhibited a great anti-inflammatory potential through the inhibition of NO production (IC50=1.72±0.91µg/mL); inihibition of 5-LOX activity (IC50=36.97±7.12µg/mL) and activation of ALP activity (IC50=0.13±0.01µg/mL) as compared to Baicalin the standard. The anti-inflammatory potential of phomopsinin A and phomopsinin A acetate were lower compared to baicalin. Conclusion: Ultimately, among compounds tested, phomopsinin B exhibited the best anti-amoebic, antibacterial and ant-inflammatory potential similar to the respective standards within the limits of the tests carried out.
从内生真菌Phomopsis sp CAM212中分离的三种天然聚酮对痢疾致病菌的抗炎和抗菌作用
目的:评价三种天然多酮类化合物CAM212的抗阿米巴、抗菌和抗炎活性。研究设计:采用临床分离的溶组织芽胞杆菌、大肠杆菌ATCC25922株、原代小鼠腹腔巨噬细胞和三种聚酮。学习地点和时间:2022年5月至12月,雅温得第一大学理学院药理学和毒理学实验室,医学微生物实验室。方法:在这项工作中,我们评估了三种天然多酮从磷藓sp抑制细菌的生长负责阿米巴和细菌性痢疾的能力。首先,对临床分离的溶组织芽胞杆菌进行了多种培养的抗阿米巴活性研究。随后,我们评估了大肠杆菌ATCC25922菌株的抗菌潜力。最后,通过抑制一氧化氮(NO)的产生、磷酸酶碱性(ALP)的激活和5-脂氧合酶(5-LOX)的抑制,在SC活化的巨噬细胞原代培养中评估其抗炎能力。结果:phomopsinin B对阿米巴的抑制作用最强(72h后抑制率为84.4%),抑菌作用最强(MIC=12.5µg/mL, MBC/MIC=2)。麻藻A和醋酸麻藻A表现出中等的抗阿米巴和抗菌潜能。但这些活性均低于甲硝唑和环丙沙星(72h后阿米巴抑制率为90%;MIC=0.72µg/mL, MBC/MIC=4)。随后,所有测试的化合物对原代巨噬细胞无毒。Phomopsinin B通过抑制NO生成显示出很强的抗炎潜能(IC50=1.72±0.91µg/mL);抑制5-LOX活性(IC50=36.97±7.12µg/mL)和ALP活性(IC50=0.13±0.01µg/mL)。与黄芩苷相比,青蒿素A和青蒿素A醋酸酯具有较低的抗炎潜能。结论:在所测化合物中,phomopsinin B的抗阿米巴、抗菌和抗炎潜能在试验范围内均达到各自标准。
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