COMPARATIVE MIC PROFILING OF COLISTIN AND POLYMYXIN B REVEALS SPECIES-SPECIFIC SUSCEPTIBILITY AND DILUTION DISCORDANCE AMONG GRAM-NEGATIVE BACTERIA
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Abstract
Resistance in Gram-negative bacteria has increased dependence on last-line drugs like colistin and polymyxin B, but their minimum inhibitory concentration (MIC) may differ across species. This study compared species-specific colistin and polymyxin B MIC profiles and quantified paired dilution agreement and discordance among Gram-negative bacterial isolates. A total of 160 isolates of Klebsiella pneumoniae, Escherichia coli, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp. were included in the retrospective quantitative study. Medians, IQR's, MIC50 and MIC90 were used to characterize MIC distributions, and non-parametric tests were used to test species differences, paired MIC differences and correlations. Overall MIC50/MIC90 values were 0.25/16 for colistin and 0.125/0.5 for polymyxin B. Colistin MICs differed significantly across species (H = 9.346, p = 0.025), whereas polymyxin B MICs did not (p = 0.434). Paired MICs differed significantly (W = 67.5, p < 0.001; r = 0.838) and showed a moderate positive correlation (ρ = 0.580, p < 0.001). Agreement was 65.6% within ±1 dilution and 77.5% within ±2 dilutions, while 22.5% of pairs differed by more than two dilution steps. These findings demonstrate related but non-equivalent MIC patterns, supporting organism-specific interpretation of colistin and polymyxin B susceptibility.
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