Role of reactive oxygen species in antibiotic action and resistance

被引:374
作者
Dwyer, Daniel J. [1 ,2 ]
Kohanski, Michael A. [1 ,2 ,3 ]
Collins, James J. [1 ,2 ,3 ]
机构
[1] Boston Univ, Howard Hughes Med Inst, Dept Biomed Engn, Ctr BioDynam, Boston, MA 02215 USA
[2] Boston Univ, Ctr Adv Biotechnol, Boston, MA 02215 USA
[3] Boston Univ, Sch Med, Boston, MA 02118 USA
关键词
BASE-EXCISION-REPAIR; POLYMERASES POL-II; ESCHERICHIA-COLI; DNA-POLYMERASES; SOS RESPONSE; OXIDATIVE DAMAGE; GENE-EXPRESSION; MUTAGENESIS; SUPEROXIDE; MECHANISMS;
D O I
10.1016/j.mib.2009.06.018
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The alarming spread of bacterial strains exhibiting resistance to current antibiotic therapies necessitates that we elucidate the specific genetic and biochemical responses underlying drug-mediated cell killing, so as to increase the efficacy of available treatments and develop new antibacterials. Recent research aimed at identifying such cellular contributions has revealed that antibiotics induce changes in metabolism that promote the formation of reactive oxygen species, which play a role in cell death. Here we discuss the relationship between drug-induced oxidative stress, the SOS response and their potential combined contribution to resistance development. Additionally, we describe ways in which these responses are being taken advantage to combat bacterial infections and arrest the rise of resistant strains.
引用
收藏
页码:482 / 489
页数:8
相关论文
共 68 条
[1]   Molecular mechanisms of antibacterial multidrug resistance [J].
Alekshun, Michael N. ;
Levy, Stuart B. .
CELL, 2007, 128 (06) :1037-1050
[2]  
[Anonymous], 2005, DNA REPAIR MUTAGENES
[3]   Fe-s cluster assembly pathways in bacteria [J].
Ayala-Castro, Carla ;
Saini, Avneesh ;
Outten, F. Wayne .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2008, 72 (01) :110-+
[4]   DNA strand breaking by the hydroxyl radical is governed by the accessible surface areas of the hydrogen atoms of the DNA backbone [J].
Balasubramanian, B ;
Pogozelski, WK ;
Tullius, TD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) :9738-9743
[5]   SOS response promotes horizontal dissemination of antibiotic resistance genes [J].
Beaber, JW ;
Hochhut, B ;
Waldor, MK .
NATURE, 2004, 427 (6969) :72-74
[6]   Oxidative decay of DNA [J].
Beckman, KB ;
Ames, BN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (32) :19633-19636
[7]   Iron uptake by Escherichia coli [J].
Braun, V .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2003, 8 :S1409-S1421
[8]   Inhibition of mutation and combating the evolution of antibiotic resistance [J].
Cirz, RT ;
Chin, JK ;
Andes, DR ;
de Crécy-Lagard, V ;
Craig, WA ;
Romesberg, FE .
PLOS BIOLOGY, 2005, 3 (06) :1024-1033
[9]   Controlling mutation: intervening in evolution as a therapeutic strategy [J].
Cirz, Ryan T. ;
Romesberg, Floyd E. .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2007, 42 (05) :341-354
[10]   Inhibition of Escherichia coli RecA by rationally redesigned N-terminal helix [J].
Cline, Daniel J. ;
Holt, Shannon L. ;
Singleton, Scott F. .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2007, 5 (10) :1525-1528