Relationships among Ciprofloxacin, Gatifloxacin, Levofloxacin, and Norfloxacin MICs for Fluoroquinolone-Resistant Escherichia coli Clinical Isolates

被引:69
作者
Boyd, Lauren Becnel [1 ]
Maynard, Merry J. [1 ]
Morgan-Linnell, Sonia K. [1 ]
Horton, Lori Banks [1 ]
Sucgang, Richard [2 ]
Hamill, Richard J. [1 ,5 ,7 ]
Jimenez, Javier Rojo [8 ]
Versalovic, James [1 ,6 ]
Steffen, David [4 ]
Zechiedrich, Lynn [1 ,2 ,3 ]
机构
[1] Baylor Coll Med, Dept Mol Virol & Microbiol, Houston, TX 77030 USA
[2] Baylor Coll Med, Verna & Marrs Mclean Dept Biochem & Mol Biol, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Pharmacol, Houston, TX 77030 USA
[4] Baylor Coll Med, Bioinformat Res Ctr, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[6] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[7] Med Ctr, Michael E DeBakey Vet Adm, Houston, TX 77030 USA
[8] Rice Univ, Dept Stat, Houston, TX 77005 USA
关键词
STAPHYLOCOCCUS-AUREUS; PSEUDOMONAS-AERUGINOSA; BACTERIAL-RESISTANCE; MUTATION-RATES; IN-VITRO; SELECTION; MUTANTS; EFFLUX; ANTIBIOTICS; STRATEGY;
D O I
10.1128/AAC.00722-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Fluoroquinolones are some of the most prescribed antibiotics in the United States. Previously, we and others showed that the fluoroquinolones exhibit a class effect with regard to the CLSI-established breakpoints for resistance, such that decreased susceptibility (i. e., an increased MIC) to one fluoroquinolone means a simultaneously decreased susceptibility to all. For defined strains, however, clear differences exist in the pharmacodynamic properties of each fluoroquinolone and the extent to which resistance-associated genotypes affect the MICs of each fluoroquinolone. In a pilot study of 920 clinical Escherichia coli isolates, we uncovered tremendous variation in norfloxacin MICs. The MICs for all of the fluoroquinolone-resistant isolates exceeded the resistance breakpoint, reaching 1,000 mu g/ml. Approximately 25% of the isolates (n = 214), representing the full range of resistant norfloxacin MICs, were selected for the simultaneous determinations of ciprofloxacin, gatifloxacin, levofloxacin, and norfloxacin MICs. We found that (i) great MIC variation existed for all four fluoroquinolones, (ii) the ciprofloxacin and levofloxacin MICs of > 90% of the fluoroquinolone-resistant isolates were higher than the resistance breakpoints, (iii) ciprofloxacin and levofloxacin MICs were distributed into two distinct groups, (iv) the MICs of two drug pairs (ciprofloxacin and norfloxacin by Kendall's Tau-b test and gatifloxacin and levofloxacin by paired t test) were similar with statistical significance but were different from each other, and (v) similar to 2% of isolates had unprecedented fluoroquinolone MIC relationships. Thus, although the fluoroquinolones can be considered equivalent with regard to clinical susceptibility or resistance, fluoroquinolone MICs differ dramatically for fluoroquinolone-resistant clinical isolates, likely because of differences in drug structure.
引用
收藏
页码:229 / 234
页数:6
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