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Antimicrobial activities of Eugenol and Cinnamaldehyde against the human gastric pathogen Helicobacter pylori

机译:丁香酚和肉桂醛对人胃病原体幽门螺杆菌的抗菌活性

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Background Eradication of Helicobacter pylori is an important objective in overcoming gastric diseases. Many regimens are currently available but none of them could achieve 100% success in eradication. Eugenol and cinnamaldehyde that are commonly used in various food preparations are known to possess antimicrobial activity against a wide spectrum of bacteria. Aim The present study was performed to assess the in vitro effects of eugenol and cinnamaldehyde against indigenous and standard H. pylori strains, their minimum inhibitory concentrations (MICs) and time course lethal effects at various pH. Methods A total of 31 strains (29 indigenous and one standard strain of H. pylori ATCC 26695, one strain of E. coli NCIM 2089) were screened. Agar dilution method was used for the determination of drug sensitivity patterns of isolates to the commonly used antibiotics and broth dilution method for the test compounds. Results Eugenol and cinnamaldehyde inhibited the growth of all the 30 H. pylori strains tested, at a concentration of 2 μg/ml, in the 9th and 12th hours of incubation respectively. At acidic pH, increased activity was observed for both the compounds. Furthermore, the organism did not develop any resistance towards these compounds even after 10 passages grown at sub-inhibitory concentrations. Conclusion These results indicate that the two bioactive compounds we tested may prevent H. pylori growth in vitro, without acquiring any resistance.
机译:背景技术根除幽门螺杆菌是克服胃病的重要目标。当前有许多方案,但没有一个方案可以100%成功地根除。众所周知,通常在各种食品制剂中使用的丁香酚和肉桂醛对多种细菌均具有抗菌活性。目的进行本研究以评估丁香酚和肉桂醛对本地和标准幽门螺杆菌菌株的体外作用,它们的最小抑菌浓度(MIC)和在不同pH下的时程致死作用。方法筛选出31株,其中29株为原产菌,一株为标准幽门螺杆菌ATCC 26695,一株为大肠杆菌NCIM 2089。琼脂稀释法用于确定分离株对常用抗生素的药物敏感性模式,肉汤稀释法用于测试化合物。结果丁香酚和肉桂醛分别在孵育的第9和12小时以2μg/ ml的浓度抑制了所有测试的30株幽门螺杆菌的生长。在酸性pH下,两种化合物的活性均得到提高。此外,即使在亚抑制浓度下生长了10次传代后,有机体也没有对这些化合物产生任何抗性。结论这些结果表明我们测试的两种生物活性化合物可能在体外阻止幽门螺杆菌生长,而没有获得任何抗药性。

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