Efflux pump inhibitors reduce the invasiveness of Pseudomonas aeruginosa

被引:59
作者
Hirakata, Yoichi [1 ,2 ,3 ]
Kondo, Akira [4 ]
Hoshino, Kazuki [5 ]
Yano, Hisakazu [1 ,2 ,3 ]
Arai, Kazuaki [1 ,2 ,3 ]
Hirotani, Ayako [2 ,3 ]
Kunishima, Hiroyuki [2 ,3 ]
Yamamoto, Natsuo [2 ,3 ]
Hatta, Masumitsu [2 ,3 ]
Kitagawa, Miho [2 ,3 ]
Kohno, Shigeru [4 ]
Kaku, Mitsuo [1 ,2 ,3 ]
机构
[1] Tohoku Univ, Dept Clin Microbiol Epidemiol Res & Management &, Grad Sch Med, Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Tohoku Univ, Dept Infect Control, Grad Sch Med, Aoba Ku, Sendai, Miyagi 9808574, Japan
[3] Tohoku Univ, Diagnost Lab, Grad Sch Med, Aoba Ku, Sendai, Miyagi 9808574, Japan
[4] Nagasaki Univ, Sch Med & Dent, Dept Internal Med 2, Nagasaki 8528501, Japan
[5] Daiichi Sankyo Co Ltd, Tokyo 1348630, Japan
关键词
Pseudomonas aeruginosa; Invasiveness; Efflux pump inhibitors; MDCK cell; New anti-infectious agent; INTRINSIC RESISTANCE; MEXAB-OPRM; SYSTEMS;
D O I
10.1016/j.ijantimicag.2009.06.007
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Efflux systems are thought to contribute to antimicrobial resistance in Pseudomonas aeruginosa. The mexAB-oprM deletion strain of P. aeruginosa PAO1 is compromised in its capacity to invade Madin-Darby canine kidney (MDCK) cells, suggesting that P. aeruginosa exports invasion determinants using a MexAB-OprM system. The influences of efflux pump inhibitors (EPIs), including the broad-spectrum EPI Phe-Arg-beta-naphthylamide (PA beta N) and MexAB-OprM-specific EPI D13-9001, on the invasion of wild-type (WT) P. aeruginosa PAO1 and its MexAB-OprM-overproducing nalB strain were examined. The invasiveness of PAO1 WT and nalB strains was inhibited in the presence of EPIs in a concentration-dependent manner. Reduction of the invasiveness of both strains was greater for D13-9001 compared with PA beta N. EPIs are thought to be useful in reducing the invasiveness and antimicrobial resistance of P. aeruginosa and thus may be promising as new anti-infectious agents. (C) 2009 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:343 / 346
页数:4
相关论文
共 11 条
[1]   Multidrug efflux systems play an important role in the invasiveness of Pseudomonas aeruginosa [J].
Hirakata, Y ;
Srikumar, R ;
Poole, K ;
Gotoh, N ;
Suematsu, T ;
Kohno, S ;
Kamihira, S ;
Hancock, REW ;
Speert, DP .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (01) :109-118
[2]   Penetration of clinical isolates of Pseudomonas aeruginosa through MDCK epithelial cell monolayers [J].
Hirakata, Y ;
Finlay, BB ;
Simpson, DA ;
Kohno, S ;
Kamihira, S ;
Speert, DP .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (02) :765-769
[3]   ROLE OF MEXA-MEXB-OPRM IN ANTIBIOTIC EFFLUX IN PSEUDOMONAS-AERUGINOSA [J].
LI, XZ ;
NIKAIDO, H ;
POOLE, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (09) :1948-1953
[4]   Contributions of MexAB-OprM and an EmrE homolog to intrinsic resistance of Pseudomonas aeruginosa to aminoglycosides and dyes [J].
Li, XZ ;
Poole, K ;
Nikaido, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (01) :27-33
[5]   Role of the multidrug efflux systems of Pseudomonas aeruginosa in organic solvent tolerance [J].
Li, XZ ;
Zhang, L ;
Poole, K .
JOURNAL OF BACTERIOLOGY, 1998, 180 (11) :2987-2991
[6]  
Li XZ, 1998, ANTIMICROB AGENTS CH, V42, P399
[7]   Identification and characterization of inhibitors of multidrug resistance efflux pumps in Pseudomonas aeruginosa:: Novel agents for combination therapy [J].
Lomovskaya, O ;
Warren, MS ;
Lee, A ;
Galazzo, J ;
Fronko, R ;
Lee, M ;
Blais, J ;
Cho, D ;
Chamberland, S ;
Renau, T ;
Leger, R ;
Hecker, S ;
Watkins, W ;
Hoshino, K ;
Ishida, H ;
Lee, VJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (01) :105-116
[8]   CROSS-RESISTANCE TO MEROPENEM, CEPHEMS, AND QUINOLONES IN PSEUDOMONAS-AERUGINOSA [J].
MASUDA, N ;
OHYA, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (09) :1847-1851
[9]  
Poole Keith, 2001, Current Topics in Medicinal Chemistry, V1, P59, DOI 10.2174/1568026013395605
[10]  
Schweizer HP, 1998, ANTIMICROB AGENTS CH, V42, P394