Unraveling the Physiological Complexities of Antibiotic Lethality

被引:193
|
作者
Dwyer, Daniel J. [1 ]
Collins, James J. [2 ,3 ,4 ,5 ]
Walker, Graham C. [6 ]
机构
[1] Univ Maryland, Inst Phys Sci & Technol, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA
[2] Boston Univ, Dept Biomed Engn, Howard Hughes Med Inst, Boston, MA 02215 USA
[3] Boston Univ, Ctr Synthet Biol, Boston, MA 02215 USA
[4] Harvard Univ, Wyss Inst, Boston, MA 02115 USA
[5] Boston Univ, Sch Med, Boston, MA 02118 USA
[6] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
antibiotics; cell death; reactive oxygen species; metabolism; pathogens; ESCHERICHIA-COLI-CELLS; OXIDATIVE STRESS; HYDROGEN-PEROXIDE; STAPHYLOCOCCUS-AUREUS; NITRIC-OXIDE; ACINETOBACTER-BAUMANNII; DNA-DAMAGE; MYCOBACTERIUM-TUBERCULOSIS; PSEUDOMONAS-AERUGINOSA; OXIDIZED NUCLEOTIDES;
D O I
10.1146/annurev-pharmtox-010814-124712
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We face an impending crisis in our ability to treat infectious disease brought about by the emergence of antibiotic-resistant pathogens and a decline in the development of new antibiotics. Urgent action is needed. This review focuses on a less well-understood aspect of antibiotic action: the complex metabolic events that occur subsequent to the interaction of antibiotics with their molecular targets and play roles in antibiotic lethality. Independent lines of evidence from studies of the action of bactericidal antibiotics on diverse bacteria collectively suggest that the initial interactions of drugs with their targets cannot fully account for the antibiotic lethality and that these interactions elicit the production of reactive oxidants including reactive oxygen species that contribute to bacterial cell death. Recent challenges to this concept are considered in the context of the broader literature of this emerging area of research. Possible ways that this new knowledge might be exploited to improve antibiotic therapy are also considered.
引用
收藏
页码:313 / 332
页数:20
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