Using a Chemical Genetic Screen to Enhance Our Understanding of the Antimicrobial Properties of Gallium against Escherichia coli

被引:17
|
作者
Gugala, Natalie [1 ]
Chatfield-Reed, Kate [2 ]
Turner, Raymond J. [1 ]
Chua, Gordon [1 ]
机构
[1] Univ Calgary, Dept Biol Sci, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
[2] Univ Hosp, Seidman Canc Ctr, 11100 Euclid Ave, Cleveland, OH 44106 USA
来源
GENES | 2019年 / 10卷 / 01期
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
Escherichia coli; gallium; antimicrobial agents; metal toxicity; metal resistance; metal-based antimicrobials; RIBONUCLEOSIDE DIPHOSPHATE REDUCTASE; OUTER-MEMBRANE PROTEIN; IRON-UPTAKE; TRANSCRIPTIONAL RESPONSE; NUCLEOTIDE-SEQUENCE; OXIDATIVE STRESS; IN-VITRO; MECHANISMS; INHIBITION; BINDING;
D O I
10.3390/genes10010034
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The diagnostic and therapeutic agent gallium offers multiple clinical and commercial uses including the treatment of cancer and the localization of tumors, among others. Further, this metal has been proven to be an effective antimicrobial agent against a number of microbes. Despite the latter, the fundamental mechanisms of gallium action have yet to be fully identified and understood. To further the development of this antimicrobial, it is imperative that we understand the mechanisms by which gallium interacts with cells. As a result, we screened the Escherichia coli Keio mutant collection as a means of identifying the genes that are implicated in prolonged gallium toxicity or resistance and mapped their biological processes to their respective cellular system. We discovered that the deletion of genes functioning in response to oxidative stress, DNA or iron-sulfur cluster repair, and nucleotide biosynthesis were sensitive to gallium, while Ga resistance comprised of genes involved in iron/siderophore import, amino acid biosynthesis and cell envelope maintenance. Altogether, our explanations of these findings offer further insight into the mechanisms of gallium toxicity and resistance in E. coli.
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页数:24
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