Small Molecule Restores Itaconate Sensitivity in Salmonella enterica: A Potential New Approach to Treating Bacterial Infections

被引:17
作者
Hammerer, Fabien [1 ]
Chang, Justin H. [1 ]
Duncan, Dustin [1 ]
Ruiz, Angel Castaneda [1 ]
Auclair, Karine [1 ]
机构
[1] McGill Univ, Dept Chem, Montreal, PQ H3A 0B8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
antibiotics; intracellular pathogen; itaconate degradation; medicinal chemistry; pantothenate; GLYOXYLATE CYCLE; ESCHERICHIA-COLI; MACROPHAGES; METABOLISM; REQUIRES; ACID; PATHOGENICITY; PSEUDOMONAS; RESISTANCE; EVOLUTION;
D O I
10.1002/cbic.201600078
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
In the context of increasing global antibiotic resistance, the need for alternative therapeutic targets is great. Although new antibiotics and resistance inhibitors provide temporary solutions, they are bound to become obsolete. In this work, we propose a new approach, coined bacterio-modulation that aims to restore macrophage potency towards bacterial strains that are able to survive in phagolysosomes. One key defense in the macrophage's arsenal is itaconate, an endogenous molecule with antimicrobial activity. Some intracellular pathogens have evolved to produce itaconate-degrading enzymes, which are required for intracellular proliferation and to promote pathogenicity. We herein present the first molecule able to resensitize Salmonella enterica to itaconate.
引用
收藏
页码:1513 / 1517
页数:5
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