In-vitro susceptibility of pathogenic and intermediate Leptospira species towards antibiotics and herb extracts.

V Ulok, L M Bilung, T M Guan, A S Tahar, R Ngui, K Apun
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Abstract

Leptospirosis is a severe and potentially fatal re-emerging zoonotic and waterborne disease caused by pathogenic and intermediate species of Leptospira. Given the high global rates of morbidity and mortality associated with this disease, there is an urgent need to explore alternative therapeutic agents to enhance treatment options. This study investigates the anti-leptospiral efficacy of several common antibiotics-penicillin G, doxycycline, ampicillin, amoxicillin, cefotaxime, chloramphenicol, and erythromycin, as well as extracts from local herbs, Hydnophytum formicarum Jack and Boesenbergia stenophylla, against pathogenic and intermediate Leptospira strains. A broth microdilution method determined the minimum inhibitory concentration (MIC) for the antibiotics and herb extracts. Both herbs were extracted using four different solvents: ethyl acetate, methanol, hexane, and chloroform. The extracts were then analysed using gas chromatography-mass spectrometry (GC-MS) to identify their phytochemical compounds. The results demonstrated that cefotaxime and erythromycin exhibited the highest anti-leptospiral activity, with MIC values of 0.2 µg/mL. This was followed by amoxicillin and ampicillin (0.2-0.39 µg/mL), penicillin G (0.39-3.13 µg/mL), chloramphenicol (0.78-3.13 µg/mL), and doxycycline (0.78-12.5 µg/mL). H. formicarum Jack and B. stenophylla extract extractions displayed the lowest MICs (62.5 µg/mL) for the ethyl acetate, methanol, and hexane extracts. They contained various phytochemical constituents, including some with anti-leptospiral properties. These findings indicate that different strains of Leptospira respond with varying levels of inhibition to the antibiotics and herb extracts studied. The extracts from H. formicarum Jack and B. stenophylla may have potential as anti-leptospiral drugs. However, further in-vivo studies are needed to better understand their efficacy against Leptospira.

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致病性和中间型钩端螺旋体对抗生素和草药提取物的体外敏感性。
钩端螺旋体病是由致病性和中间种钩端螺旋体引起的一种严重和可能致命的再次出现的人畜共患病和水传播疾病。鉴于与该疾病相关的全球高发病率和死亡率,迫切需要探索替代治疗药物以加强治疗选择。本研究考察了几种常用的抗生素——青霉素G、强力霉素、氨苄西林、阿莫西林、头孢噻肟、氯霉素和红霉素,以及当地草药水杨和窄叶草提取物对致病性和中间型钩端螺旋体菌株的抗钩端螺旋体疗效。用微量肉汤稀释法测定了抗生素和草药提取物的最低抑菌浓度。两种草药分别用四种不同的溶剂提取:乙酸乙酯、甲醇、己烷和氯仿。然后使用气相色谱-质谱(GC-MS)对提取物进行分析,以确定其植物化学成分。结果表明,头孢噻肟和红霉素的抗钩端螺旋体活性最高,MIC值为0.2µg/mL。其次是阿莫西林和氨苄西林(0.2-0.39µg/mL)、青霉素g(0.39-3.13µg/mL)、氯霉素(0.78-3.13µg/mL)和强力霉素(0.78-12.5µg/mL)。乙酸乙酯、甲醇和己烷提取物的mic最低(62.5µg/mL)。它们含有多种植物化学成分,包括一些具有抗钩端螺旋体特性的成分。这些结果表明,不同的钩端螺旋体菌株对所研究的抗生素和草药提取物有不同程度的抑制反应。密螺旋体和窄叶螺旋体提取物可能具有开发抗钩端螺旋体药物的潜力。然而,需要进一步的体内研究来更好地了解它们对钩端螺旋体的疗效。
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