Influence of pH on adaptive resistance of Pseudomonas aeruginosa to aminoglycosides and their postantibiotic effects

被引:34
作者
Xiong, YQ [1 ]
Caillon, J [1 ]
Drugeon, H [1 ]
Potel, G [1 ]
Baron, D [1 ]
机构
[1] CTR HOSP UNIV,FAC MED,LAB ANTIBIOL CLIN & EXPTL,F-44035 NANTES,FRANCE
关键词
D O I
10.1128/AAC.40.1.35
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adaptive resistance to aminoglycosides in Pseudomonas aeruginosa and other gram-negative bacilli is usually induced by the initial exposure to the drug. We investigated the influence of pH on the adaptive resistance of a clinical P. aeruginosa strain to aminoglycosides in vitro and on their postantibiotic effects, For adaptive resistance, the first-exposure concentrations of both amikacin and netilmicin were one, two, four, and eight times the MIC of each drug and the second-exposure concentrations were two times the MIC of each drug, Adaptive resistance was greater and more prolonged with higher initial aminoglycoside concentrations, and the bactericidal effects of the aminoglycosides were concentration dependent at pH 7.4, At pH 6.5, the killing rates of amikacin and netilmicin were far lower than those observed at pH 7.4, At pH 5.5, amikacin and netilmicin exerted practically no bactericidal effect on the P. aeruginosa strain used, However, with media at pH 5.5 and 6.5, adaptive resistance of P, aeruginosa preexposed to amikacin and netilmicin was also clearly exhibited, with the degree of adaptive resistance depending on the bactericidal effects of both drugs on nonpreexposed controls, Maximal adaptive resistance occurred between 0 and 4 h after preexposure. The postantibiotic effects of amikacin and netilmicin against the P, aeruginosa strain were shown to be concentration dependent and were reduced at acidic pHs, No changes in outer and inner membrane proteins occurred during the adaptive-resistance interval.
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页码:35 / 39
页数:5
相关论文
共 18 条
[1]  
AMSTERDAM D, 1991, ANTIBIOTICS LAB MED, P53
[2]   ADAPTIVE RESISTANCE FOLLOWING SINGLE DOSES OF GENTAMICIN IN A DYNAMIC INVITRO MODEL [J].
BARCLAY, ML ;
BEGG, EJ ;
CHAMBERS, ST .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (09) :1951-1957
[3]   ROLES OF RIBOSOMAL-BINDING, MEMBRANE-POTENTIAL, AND ELECTRON-TRANSPORT IN BACTERIAL UPTAKE OF STREPTOMYCIN AND GENTAMICIN [J].
BRYAN, LE ;
KWAN, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1983, 23 (06) :835-845
[4]  
Craig W.A., 1991, Antibiotics in Laboratory Medicine, V3rd ed., P403
[5]   ADAPTIVE RESISTANCE TO AMINOGLYCOSIDE ANTIBIOTICS FROM 1ST-EXPOSURE DOWN-REGULATION [J].
DAIKOS, GL ;
JACKSON, GG ;
LOLANS, VT ;
LIVERMORE, DM .
JOURNAL OF INFECTIOUS DISEASES, 1990, 162 (02) :414-420
[6]   1ST-EXPOSURE ADAPTIVE RESISTANCE TO AMINOGLYCOSIDE ANTIBIOTICS INVIVO WITH MEANING FOR OPTIMAL CLINICAL USE [J].
DAIKOS, GL ;
LOLANS, VT ;
JACKSON, GG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (01) :117-123
[7]   ROLE OF THE MEMBRANE-POTENTIAL IN BACTERIAL-RESISTANCE TO AMINOGLYCOSIDE ANTIBIOTICS [J].
DAMPER, PD ;
EPSTEIN, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1981, 20 (06) :803-808
[8]  
DAVIES JE, 1991, ANTIBIOTICS LAB MED, P691
[9]   QUANTITATIVE ASSOCIATION BETWEEN ELECTRICAL POTENTIAL ACROSS THE CYTOPLASMIC MEMBRANE AND EARLY GENTAMICIN UPTAKE AND KILLING IN STAPHYLOCOCCUS-AUREUS [J].
EISENBERG, ES ;
MANDEL, LJ ;
KABACK, HR ;
MILLER, MH .
JOURNAL OF BACTERIOLOGY, 1984, 157 (03) :863-867
[10]   TOBRAMYCIN UPTAKE IN ESCHERICHIA-COLI IS DRIVEN BY EITHER ELECTRICAL POTENTIAL OR ATP [J].
FRAIMOW, HS ;
GREENMAN, JB ;
LEVITON, IM ;
DOUGHERTY, TJ ;
MILLER, MH .
JOURNAL OF BACTERIOLOGY, 1991, 173 (09) :2800-2808