A global view of antibiotic resistance

被引:240
作者
Luis Martinez, Jose [1 ,2 ]
Fajardo, Alicia [1 ,2 ]
Garmendia, Leonor [1 ,2 ]
Hernandez, Alvaro [1 ,2 ]
Francisco Linares, Juan [1 ,2 ]
Martinez-Solano, Laura [1 ,2 ]
Blanca Sanchez, Maria [1 ,2 ]
机构
[1] CSIC, Dept Biotecnol Microbiana, Ctr Nacl Biotecnol, Madrid 28049, Spain
[2] CIBERESP, Sao Paulo, Brazil
关键词
antibiotic resistance; bacterial evolution; fitness cost; hypermutation; horizontal gene transfer; HGT; MULTIDRUG EFFLUX PUMP; ENTERICA SEROVAR TYPHIMURIUM; HYPERMUTABLE PSEUDOMONAS-AERUGINOSA; SMALL-COLONY VARIANTS; DNA-POLYMERASE-IV; ESCHERICHIA-COLI; SALMONELLA-ENTERICA; GENE-EXPRESSION; STENOTROPHOMONAS-MALTOPHILIA; STREPTOCOCCUS-PNEUMONIAE;
D O I
10.1111/j.1574-6976.2008.00142.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Antibiotic resistance is one of the few examples of evolution that can be addressed experimentally. The present review analyses this resistance, focusing on the networks that regulate its acquisition and its effect on bacterial physiology. It is widely accepted that antibiotics and antibiotic resistance genes play fundamental ecological roles - as weapons and shields, respectively - in shaping the structures of microbial communities. Although this Darwinian view of the role of antibiotics is still valid, recent work indicates that antibiotics and resistance mechanisms may play other ecological roles and strongly influence bacterial physiology. The expression of antibiotic resistance determinants must therefore be tightly regulated and their activity forms part of global metabolic networks. In addition, certain bacterial modes of life can trigger transient phenotypic antibiotic resistance under some circumstances. Understanding resistance thus requires the analysis of the regulatory networks controlling bacterial evolvability, the physiological webs affected and the metabolic rewiring it incurs.
引用
收藏
页码:44 / 65
页数:22
相关论文
共 278 条
[1]   The MexGHI-OpmD multidrug efflux pump controls growth, antibiotic susceptibility and virulence in Pseudomonas aeruginosa via 4-quinolone-dependent cell-to-cell communication [J].
Aendekerk, S ;
Diggle, SP ;
Song, Z ;
Hoiby, N ;
Cornelis, P ;
Williams, P ;
Cámara, M .
MICROBIOLOGY-SGM, 2005, 151 :1113-1125
[2]   EFFECTS OF CIPROFLOXACIN ON PLASMID DNA SUPERCOILING OF ESCHERICHIA-COLI TOPOISOMERASE-I AND GYRASE MUTANTS [J].
ALEIXANDRE, V ;
HERRERA, G ;
URIOS, A ;
BLANCO, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (01) :20-23
[3]   Molecular mechanisms of antibacterial multidrug resistance [J].
Alekshun, Michael N. ;
Levy, Stuart B. .
CELL, 2007, 128 (06) :1037-1050
[4]   Regulation of chromosomally mediated multiple antibiotic resistance: the mar regulon [J].
Alekshun, MN ;
Levy, SB .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (10) :2067-2075
[5]   The mar regulon:: multiple resistance to antibiotics and other toxic chemicals [J].
Alekshun, MN ;
Levy, SB .
TRENDS IN MICROBIOLOGY, 1999, 7 (10) :410-413
[6]   Characterization of colony morphology variants isolated from Streptococcus pneumoniae biofilms [J].
Allegrucci, Magee ;
Sauer, Karin .
JOURNAL OF BACTERIOLOGY, 2007, 189 (05) :2030-2038
[7]   Cloning and characterization of SmeDEF, a novel multidrug efflux pump from Stenotrophomonas maltophilia [J].
Alonso, A ;
Martínez, JL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (11) :3079-3086
[8]   Overexpression of the multidrug efflux pump SmeDEF impairs Stenotrophomonas maltophilia physiology [J].
Alonso, A ;
Morales, G ;
Escalante, R ;
Campanario, E ;
Sastre, L ;
Martinez, JL .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 53 (03) :432-434
[9]   Multiple antibiotic resistance in Stenotrophomonas maltophilia [J].
Alonso, A ;
Martinez, JL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (05) :1140-1142
[10]   Environmental and clinical isolates of Pseudomonas aeruginosa show pathogenic and biodegradative properties irrespective of their origin [J].
Alonso, A ;
Rojo, F ;
Martínez, JL .
ENVIRONMENTAL MICROBIOLOGY, 1999, 1 (05) :421-430