The Effect of Dillapiole on the pathogenesis of Escherichia coli

K. Bailey
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Abstract

Dillapiole, a compound isolated from the plant, Foeniculum vulgare (Fennel, Hinojo), was previously discovered to have been effective at diminishing virulence factor expression of Francisella tularensis, a gram-negative bacterium with bioterror potential. The purpose of this work is to examine the therapeutic potential of dillapiole on other pathogenic bacteria such as Escherichia coli. E. coli is a motile, rod-shaped, gram-negative bacterium that is typically found in the intestines of animals and humans and can be an opportunistic pathogen. With the increase of multi-drug resistance among various bacteria, it is important for further research on new therapeutic agents. As in previous studies involving F. tularensis, data presented here suggest that dillapiole does not directly diminish the viability of E. coli.  Dubia cockroach infection assays were used to evaluate the ability of dillapiole to dampen the pathogenesis of E. coli.  Roaches infected with E. coli that were subsequently treated with dillapiole exhibited similar survival to those treated with tetracycline.  However, cockroaches that were treated with the vehicle (DMSO) exhibited reduced levels of survival.  This finding suggests that dillapiole might be dampening E. coli pathogenesis or could be modulating cockroach immunity.  Ongoing studies are focusing on the effect of dillapiole on E. coli virulence gene expression (Supported by NIH Grant P20GM103434 to the West Virginia IDeA Network for Biomedical Research Excellence).
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dillapole对大肠杆菌发病机制的影响
Dillapiole是一种从茴香植物Foeniculum vulgare(茴香,Hinojo)中分离出来的化合物,以前发现它可以有效地降低土拉弗朗西斯菌的毒力因子表达,土拉弗朗西斯菌是一种具有生物恐怖潜力的革兰氏阴性细菌。本工作的目的是研究dillapole对其他致病菌如大肠杆菌的治疗潜力。大肠杆菌是一种可运动的杆状革兰氏阴性细菌,通常存在于动物和人类的肠道中,可能是一种机会性病原体。随着各种细菌的多重耐药现象的增加,进一步研究新的治疗药物具有重要意义。正如先前涉及土拉菌的研究一样,本文提供的数据表明,dillapole不会直接降低大肠杆菌的生存能力。采用杜比亚蜚蠊感染试验,评价dillapole抑制大肠杆菌发病的能力。感染大肠杆菌的蟑螂随后用dillapole治疗,其存活率与用四环素治疗的蟑螂相似。然而,用载体(DMSO)处理的蟑螂表现出较低的存活率。这一发现表明dillapole可能抑制了大肠杆菌的发病机制或调节了蟑螂的免疫力。正在进行的研究主要集中在dillapole对大肠杆菌毒力基因表达的影响(由NIH资助P20GM103434资助西弗吉尼亚IDeA生物医学研究卓越网络)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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