Mutant prevention concentrations of ciprofloxacin for urinary tract infection isolates of Escherichia coli

被引:69
作者
Marcusson, LL
Olofsson, SK
Lindgren, PK
Cars, O
Hughes, D
机构
[1] Uppsala Univ, Ctr Biomed, Dept Cell & Mol Biol, S-75124 Uppsala, Sweden
[2] Uppsala Univ, Dept Med Sci, S-75122 Uppsala, Sweden
关键词
MPC; UTI; E; coli; mutant selection window;
D O I
10.1093/jac/dki136
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To measure the mutant prevention concentration (MPC) of ciprofloxacin for a set of urinary tract infection (UTI) Escherichia coli isolates with different levels of susceptibility and determine whether MPC can be predicted from MIC. Methods: MPC was defined as the lowest ciprofloxacin concentration that prevented the growth of resistant colonies when 1010 bacteria were spread on solid medium and incubated for 96 h at 37 degrees C. MIC was measured by Etest. Bacteria surviving (persisting) at MPC were isolated and quantified from agar plugs taken after 96h. The genes hipA and hipB were amplified by PCR from persisters and sequenced. Results: Isolates with MICs above the NCCLS breakpoint for ciprofloxacin resistance (4 mg/L) typically have MPCs greater than 32mg/L. Isolates with MICs below the breakpoint for ciprofloxacin susceptibility (1 mg/L) have MPCs up to 5 mg/L. MPC/MIC is similar to 16 for most susceptible isolates but there are several notable exceptions (MPC/MIC > 100). Resistant colonies arising one dilution step below MPC often had MIC > MPC. In every case tested, a proportion of cells survived (persisted), but did not grow into colonies, at MPC, without any increase in MIC. Conclusions: MPCs were determined for all ciprofloxacin-susceptible isolates. MPC is not accurately predicted from MIC. Colonies selected below MPC frequently have MIC > MPC, suggesting multiple mutations. A small fraction of cells from all strains tested survived for 96 h at MPC, without any associated increase in MIC. These survivors/persisters are not hipAB mutants.
引用
收藏
页码:938 / 943
页数:6
相关论文
共 51 条
[31]   Effect of chloramphenicol, erythromycin, moxifloxacin, penicillin and tetracycline concentration on the recovery of resistant mutants of Mycobacterium smegmatis and Staphylococcus aureus [J].
Lu, T ;
Zhao, XL ;
Li, XY ;
Hansen, G ;
Blondeau, J ;
Drlica, K .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 52 (01) :61-64
[32]   Quinolone resistance from a transferable plasmid [J].
Martínez-Martínez, L ;
Pascual, A ;
Jacoby, GA .
LANCET, 1998, 351 (9105) :797-799
[33]   HIPA, A NEWLY RECOGNIZED GENE OF ESCHERICHIA-COLI K-12 THAT AFFECTS FREQUENCY OF PERSISTENCE AFTER INHIBITION OF MUREIN SYNTHESIS [J].
MOYED, HS ;
BERTRAND, KP .
JOURNAL OF BACTERIOLOGY, 1983, 155 (02) :768-775
[34]   Establishment of a persistent Escherichia coli reservoir during the acute phase of a bladder infection [J].
Mulvey, MA ;
Schilling, JD ;
Hultgren, SJ .
INFECTION AND IMMUNITY, 2001, 69 (07) :4572-4579
[35]   EAU guidelines for the management of urinary and male genital tract infections - Urinary Tract Infection (UTI) Working Group of the Health Care Office (HCO) of the European Association of Urology (EAU) [J].
Naber, KG ;
Bergman, B ;
Bishop, MC ;
Bjerklund-Johansen, TE ;
Botto, H ;
Lobel, B ;
Cruz, FJ ;
Selvaggi, FP .
EUROPEAN UROLOGY, 2001, 40 (05) :576-588
[36]   Concentration-dependent selection of small phenotypic differences in TEM β-lactamase-mediated antibiotic resistance [J].
Negri, MC ;
Lipsitch, M ;
Blázquez, J ;
Levin, BR ;
Baquero, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (09) :2485-2491
[37]   Ineffectiveness of topoisomerase mutations in mediating clinically significant fluoroquinolone resistance in Escherichia coli in the absence of the AcrAB efflux pump [J].
Oethinger, M ;
Kern, WV ;
Jellen-Ritter, AS ;
McMurry, LM ;
Levy, SB .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (01) :10-13
[38]   Adaptive point mutation and adaptive amplification pathways in the Escherichia coli Lac system:: Stress responses producing genetic change [J].
Rosenberg, SM ;
Hastings, PJ .
JOURNAL OF BACTERIOLOGY, 2004, 186 (15) :4838-4843
[39]   Adaptive mutation:: How growth under selection stimulates Lac+ reversion by increasing target copy number [J].
Roth, JR ;
Andersson, DI .
JOURNAL OF BACTERIOLOGY, 2004, 186 (15) :4855-4860
[40]   CONDITIONAL IMPAIRMENT OF CELL-DIVISION AND ALTERED LETHALITY IN HIPA MUTANTS OF ESCHERICHIA-COLI K-12 [J].
SCHERRER, R ;
MOYED, HS .
JOURNAL OF BACTERIOLOGY, 1988, 170 (08) :3321-3326