Inhibitors of efflux pumps in Gram-negative bacteria

被引:183
作者
Pagès, JM
Masi, M
Barbe, J
机构
[1] Univ Mediterranee, Fac Med, IFR48, EA2197, F-13385 Marseille, France
[2] Univ Mediterranee, Fac Pharm, IFR48, CNRS,UMR6178,GERCTOP, F-13385 Marseille, France
关键词
D O I
10.1016/j.molmed.2005.06.006
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
In Gram-negative bacteria, efflux complexes, consisting of an inner-membrane pump, a periplasmic adaptor protein and outer-membrane channel, provide an efficient means for the export of structurally unrelated drugs, causing the multidrug-resistance phenotype. Resistance due to this antibiotic efflux is an increasing problem worldwide. A new molecular challenge is to combat this transport by searching for new molecules to block efflux and thus restore drug susceptibility to resistant clinical strains. Recent data shed new light on the structure and activity of the archetypal efflux pumps AcrAB-ToIC and MexAB-OprM. Here, we describe recent insights into the molecular mechanisms of bacterial efflux pumps and their inhibitors. Current progress for the clinical use of efflux-pump inhibitors and new strategies to combat the drug-efflux mechanisms will be discussed.
引用
收藏
页码:382 / 389
页数:8
相关论文
共 70 条
[51]   The AcrAB-TolC efflux pump contributes to multidrug resistance in the nosocomial pathogen Enterobacter aerogenes [J].
Pradel, E ;
Pagès, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (08) :2640-2643
[52]   Bile-salt-mediated induction of antimicrobial and bile resistance in Salmonella typhimurium [J].
Prouty, AM ;
Brodsky, IE ;
Falkow, S ;
Gunn, JS .
MICROBIOLOGY-SGM, 2004, 150 :775-783
[53]   Conformationally-restricted analogues of efflux pump inhibitors that potentiate the activity of levofloxacin in Pseudomonas aeruginosa [J].
Renau, TE ;
Léger, R ;
Filonova, L ;
Flamme, EM ;
Wang, M ;
Yen, R ;
Madsen, D ;
Griffith, D ;
Chamberland, S ;
Dudley, MN ;
Lee, VJ ;
Lomovskaya, O ;
Watkins, WJ ;
Ohta, T ;
Nakayama, K ;
Ishida, Y .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (16) :2755-2758
[54]   Peptidomimetics of efflux pump inhibitors potentiate the activity of levofloxacin in Pseudomonas aeruginosa [J].
Renau, TE ;
Léger, R ;
Yen, R ;
She, MW ;
Flamme, EM ;
Sangalang, J ;
Gannon, CL ;
Chamberland, S ;
Lomovskaya, O ;
Lee, VJ .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (05) :763-766
[55]   Effect of an efflux pump inhibitor on the MIC of nalidixic acid for Acinetobacter baumannii and Stenotrophomonas maltophilia clinical isolates [J].
Ribera, A ;
Ruiz, J ;
de Anta, MTJ ;
Vila, J .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 (04) :697-U10
[56]   Bile salts and fatty acids induce the expression of Escherichia coli AcrAB multidrug efflux pump through their interaction with Rob regulatory protein [J].
Rosenberg, EY ;
Bertenthal, D ;
Nilles, ML ;
Bertrand, KP ;
Nikaido, H .
MOLECULAR MICROBIOLOGY, 2003, 48 (06) :1609-1619
[57]   Phylogeny of multidrug transporters [J].
Saier, MH ;
Paulsen, IT .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2001, 12 (03) :205-213
[58]   The efflux pump inhibitor Phe-Arg-β-naphthylamide does not abolish the activity of the Stenotrophomonas maltophilia SmeDEF multidrug efflux pump [J].
Sánchez, P ;
Le, U ;
Martínez, JL .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (04) :1042-1045
[59]   Role of AcrR and RamA in fluoroquinolone resistance in clinical Klebsiella pneumoniae isolates from Singapore [J].
Schneiders, T ;
Amyes, SGB ;
Levy, SB .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (09) :2831-2837
[60]   Antiinfective biotechs face partnering gap [J].
Sheridan, C .
NATURE BIOTECHNOLOGY, 2005, 23 (02) :155-156