Carbapenem activities against Pseudomonas aeruginosa:: Respective contributions of OprD and efflux systems

被引:222
作者
Köhler, T [1 ]
Michea-Hamzehpour, M [1 ]
Epp, SF [1 ]
Pechere, JC [1 ]
机构
[1] Ctr Med Univ Geneva, Dept Genet & Microbiol, CH-1211 Geneva 4, Switzerland
关键词
D O I
10.1128/AAC.43.2.424
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
While meropenem MICs were strongly influenced by the presence or absence of the MexAB-OprM efflux pump in both OprD-proficient and -deficient strain backgrounds, MICs of imipenem and of ER-35786 remained unchanged, demonstrating that meropenem is a substrate of MexAB-OprM but not imipenem and ER-35786. In vitro, all three carbapenems selected loss of OprD as a first mechanism of resistance. However, in an OprD-deficient background, meropenem was able to select MexAB-OprM overproducers as a secondary resistance mechanism, while ER-35786 selected a mutant cross-resistant to sparfloxacin and cefpirome.
引用
收藏
页码:424 / 427
页数:4
相关论文
共 26 条
  • [1] OUTER-MEMBRANE PERMEABILITY IN PSEUDOMONAS-AERUGINOSA - COMPARISON OF A WILD-TYPE WITH AN ANTIBIOTIC-SUPERSUSCEPTIBLE MUTANT
    ANGUS, BL
    CAREY, AM
    CARON, DA
    KROPINSKI, AMB
    HANCOCK, REW
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1982, 21 (02) : 299 - 309
  • [2] MECHANISMS OF RESISTANCE TO BETA-LACTAM ANTIBIOTICS AMONGST PSEUDOMONAS-AERUGINOSA ISOLATES COLLECTED IN THE UK IN 1993
    CHEN, HY
    YUAN, M
    LIVERMORE, DM
    [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 1995, 43 (04) : 300 - 309
  • [3] Epp S, UNPUB
  • [4] ACTIVITY OF CARBAPENEM BMS-181139 AGAINST PSEUDOMONAS-AERUGINOSA IS NOT DEPENDENT ON PORIN PROTEIN D2
    FUNGTOMC, JC
    GRADELSKI, E
    KOLEK, B
    MINASSIAN, B
    PUCCI, M
    KESSLER, RE
    BONNER, DP
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (02) : 386 - 393
  • [5] Characterization of the MexC-MexD-OprJ multidrug efflux system in ΔmexA-mexB-oprM mutants of Pseudomonas aeruginosa
    Gotoh, N
    Tsujimoto, H
    Tsuda, M
    Okamoto, K
    Nomura, A
    Wada, T
    Nakahashi, M
    Nishino, T
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (08) : 1938 - 1943
  • [6] GENETIC ORGANIZATION OF ARGININE-BIOSYNTHESIS IN PSEUDOMONAS-AERUGINOSA
    HAAS, D
    HOLLOWAY, BW
    SCHAMBOCK, A
    LEISINGER, T
    [J]. MOLECULAR & GENERAL GENETICS, 1977, 154 (01): : 7 - 22
  • [7] JORGENSEN JH, 1997, METHODS DILUTION ANT
  • [8] Differential selection of multidrug efflux systems by quinolones in Pseudomonas aeruginosa
    Kohler, T
    MicheaHamzehpour, M
    Plesiat, P
    Kahr, AL
    Pechere, JC
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (11) : 2540 - 2543
  • [9] Characterization of MexE-MexF-OprN, a positively regulated multidrug efflux system of Pseudomonas aeruginosa
    Kohler, T
    MicheaHamzehpour, M
    Henze, U
    Gotoh, N
    Curty, LK
    Pechere, JC
    [J]. MOLECULAR MICROBIOLOGY, 1997, 23 (02) : 345 - 354
  • [10] ROLE OF MEXA-MEXB-OPRM IN ANTIBIOTIC EFFLUX IN PSEUDOMONAS-AERUGINOSA
    LI, XZ
    NIKAIDO, H
    POOLE, K
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (09) : 1948 - 1953