Bacterial antibiotic efflux systems of medical importance

被引:64
作者
Köhler, T
Pechère, JC
Plésiat, P
机构
[1] Ctr Med Univ Geneva, Dept Genet & Microbiol, CH-1211 Geneva 4, Switzerland
[2] Univ Hosp Ctr Besancon, F-25030 Besancon, France
关键词
multidrug resistance; microorganisms; efflux; resistance mechanism;
D O I
10.1007/s000180050024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multidrug efflux systems endow on bacterial cells the ability to limit the access of antimicrobial agents to their targets. By actively pumping out antibiotic molecules, these systems prevent the intracellular accumulation necessary for antibiotics to exert their lethal activity. Drug efflux appears to be one of the most widespread antibiotic resistance mechanisms among microorganisms, since it has been demonstrated to occur in many Gram-positive and Gram-negative bacteria including medically important species like staphylococci, streptococci, enterobacteria and opportunistic pathogens like Pseudomonas aeruginosa. Efflux pumps can be specific for only one substrate or accommodate a more or less wide range of noxious products. Export of structurally unrelated compounds confers a multidrug-resistance phenotype on bacterial cells. Therapeutically critical levels of resistance can be achieved by overexpression of efflux systems, especially in those species such as P. aeruginosa which possess a low outer membrane permeability. It is suspected that the dual physiological function of active efflux systems is both the secretion of intracellular metabolites and the protection against a variety of harmful substances that the microorganism may encounter in its natural environment.
引用
收藏
页码:771 / 778
页数:8
相关论文
共 62 条
  • [1] EMERGENCE OF QUINOLONE-IMIPENEM CROSS-RESISTANCE IN PSEUDOMONAS-AERUGINOSA AFTER FLUOROQUINOLONE THERAPY
    AUBERT, G
    POZZETTO, B
    DORCHE, G
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1992, 29 (03) : 307 - 312
  • [2] Prevalence of a putative efflux mechanism among fluoroquinolone-resistant clinical isolates of Streptococcus pneumoniae
    Brenwald, NP
    Gill, MJ
    Wise, R
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (08) : 2032 - 2035
  • [3] ROLE OF MUTATIONS IN DNA GYRASE GENES IN CIPROFLOXACIN RESISTANCE OF PSEUDOMONAS-AERUGINOSA SUSCEPTIBLE OR RESISTANT TO IMIPENEM
    CAMBAU, E
    PERANI, E
    DIB, C
    PETINON, C
    TRIAS, J
    JARLIER, V
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (10) : 2248 - 2252
  • [4] Molecular cloning and functional analysis of a novel macrolide-resistance determinant, mefA, from Streptococcus pyogenes
    Clancy, J
    Petitpas, J
    DibHajj, F
    Yuan, W
    Cronan, M
    Kamath, AV
    Bergeron, J
    Retsema, JA
    [J]. MOLECULAR MICROBIOLOGY, 1996, 22 (05) : 867 - 879
  • [5] DISTRIBUTION OF GENES ENCODING ERYTHROMYCIN RIBOSOMAL METHYLASES AND AN ERYTHROMYCIN EFFLUX PUMP IN EPIDEMIOLOGICALLY DISTINCT GROUPS OF STAPHYLOCOCCI
    EADY, EA
    ROSS, JI
    TIPPER, JL
    WALTERS, CE
    COVE, JH
    NOBLE, WC
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1993, 31 (02) : 211 - 217
  • [6] FRAIMOV, 1997, ASM ABSTR
  • [7] NFXC-TYPE QUINOLONE RESISTANCE IN A CLINICAL ISOLATE OF PSEUDOMONAS-AERUGINOSA
    FUKUDA, H
    HOSAKA, M
    IYOBE, S
    GOTOH, N
    NISHINO, T
    HIRAI, K
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (03) : 790 - 792
  • [8] Identification of an efflux pump gene, pmrA, associated with fluoroquinolone resistance in Streptococcus pneumoniae
    Gill, MJ
    Brenwald, NP
    Wise, R
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (01) : 187 - 189
  • [9] THE TET(K) GENE OF PLASMID PT181 OF STAPHYLOCOCCUS-AUREUS ENCODES AN EFFLUX PROTEIN THAT CONTAINS 14 TRANSMEMBRANE HELICES
    GUAY, GG
    KHAN, SA
    ROTHSTEIN, DM
    [J]. PLASMID, 1993, 30 (02) : 163 - 166
  • [10] RESISTANCE OF NEISSERIA-GONORRHOEAE TO ANTIMICROBIAL HYDROPHOBIC AGENTS IS MODULATED BY THE MTRRCDE EFFLUX SYSTEM
    HAGMAN, KE
    PAN, WB
    SPRATT, BG
    BALTHAZAR, JT
    JUDD, RC
    SHAFER, WM
    [J]. MICROBIOLOGY-SGM, 1995, 141 : 611 - 622