Claire O. Kelly, E. Young, J. Gibson, S. McGovern, Emma Beatty, Kendall Soulder, J. Rice, Ryan J. Percifield, D. Primerano, Nicole L. Garrison, Deanna M Schmitt
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Whole genome sequencing of resazurin-resistant (Rzr) Ft LVS mutants revealed four mutations found in 93% of the isolates sequenced. Three mutations were within the coding regions of FTL_0421, FTL_0895, and FTL_1504 and the other mutation was 50 bp upstream of FTL_0445, likely disrupting expression of this gene. The focus of my project was to explore the role of FTL_0895 in resazurin susceptibility. To confirm this gene plays a role in the reduced susceptibility of the Rzr strains to resazurin, we cloned the wild-type copy of FTL_0895 into the Francisella vector pABST which contains the robust groE promotor of Ft. The resulting plasmid will be electroporated into one of the Rzr mutants and we will test the susceptibility of the complemented strain to resazurin, using time kill and agar dilution assays. 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To confirm this gene plays a role in the reduced susceptibility of the Rzr strains to resazurin, we cloned the wild-type copy of FTL_0895 into the Francisella vector pABST which contains the robust groE promotor of Ft. The resulting plasmid will be electroporated into one of the Rzr mutants and we will test the susceptibility of the complemented strain to resazurin, using time kill and agar dilution assays. 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引用次数: 0
摘要
对抗生素治疗的耐药性,加上抗生素发现的减少,导致一度“可治愈”的细菌感染造成的死亡人数稳步增加。开发新药对于防止未来更多的生命损失至关重要。我们发现化合物reazurin对革兰氏阴性菌包括土拉菌Francisella tularensis (Ft)具有抗菌活性,然而,某些菌株对reazurin产生了耐药性。了解Ft如何对瑞祖菌素产生耐药性将有助于确定瑞祖菌素引发其抗菌作用的机制。reazurin -resistant (Rzr) Ft LVS突变体的全基因组测序显示,在93%的测序分离株中发现4个突变。三个突变位于FTL_0421、FTL_0895和FTL_1504编码区,另一个突变位于FTL_0445上游50 bp,可能破坏了该基因的表达。我的项目重点是探索FTL_0895在resazurin易感性中的作用。为了证实该基因在降低Rzr菌株对resazurin的敏感性中起作用,我们将FTL_0895的野生型拷贝克隆到含有Ft强健groE启动子的Francisella载体pABST中。所得到的质粒将被电孔插入其中一个Rzr突变体中,我们将使用时间杀死和agar稀释试验来测试补充菌株对resazurin的敏感性。如果补充菌株对resazurin的敏感性恢复,则可以确定FTL_0895是resazurin的潜在靶点。
Role of FTL_0895 in Francisella tularensis Susceptibility to Resazurin.
Resistance to antibiotic treatments coupled with the decline in antibiotic discovery has resulted in a steady increase in deaths caused by once “curable” bacterial infections. Developing new drugs is crucial to prevent more loss of life in the future. We discovered the compound resazurin exhibits antimicrobial activity against gram-negative bacteria including Francisella tularensis (Ft), however, certain strains of Ft have developed resistance to resazurin. Understanding how Ft develops resistance to resazurin will help with defining the mechanism by which resazurin elicits its antimicrobial effect. Whole genome sequencing of resazurin-resistant (Rzr) Ft LVS mutants revealed four mutations found in 93% of the isolates sequenced. Three mutations were within the coding regions of FTL_0421, FTL_0895, and FTL_1504 and the other mutation was 50 bp upstream of FTL_0445, likely disrupting expression of this gene. The focus of my project was to explore the role of FTL_0895 in resazurin susceptibility. To confirm this gene plays a role in the reduced susceptibility of the Rzr strains to resazurin, we cloned the wild-type copy of FTL_0895 into the Francisella vector pABST which contains the robust groE promotor of Ft. The resulting plasmid will be electroporated into one of the Rzr mutants and we will test the susceptibility of the complemented strain to resazurin, using time kill and agar dilution assays. If the susceptibility of the complemented strain to resazurin is restored, then it can be determined that FTL_0895 is a potential target of resazurin.