Apotransferrin in Combination with Ciprofloxacin Slows Bacterial Replication, Prevents Resistance Amplification, and Increases Antimicrobial Regimen Effect [Experimental Therapeutics]

There has been a renewed interest in combining traditional small-molecule antimicrobial agents with non-traditional therapies to potentiate antimicrobial effects. Apotransferrin, which decreases iron availability to microbes, is one such approach. We conducted a 48-h one-compartment in vitro infection model to explore the impact of apotransferrin on the bactericidal activity of ciprofloxacin. The challenge panel included four Klebsiella pneumoniae isolates, with ciprofloxacin minimum inhibitory concentrations (MIC) values ranging from 0.08 to 32 mg/L. Each challenge isolate was subjected to an ineffective ciprofloxacin monotherapy exposure (free-drug area under the concentration-time curve over 24 h divided by the MIC [AUC:MIC ratio] ranging from 0.19 to 96.6) with and without apotransferrin. As expected, the no-treatment and apotransferrin control arms showed unaltered, prototypical logarithmic bacterial growth. We identified relationships between exposure and change in bacterial density for ciprofloxacin alone (R² = 0.64) and ciprofloxacin in combination with apotransferrin (R² = 0.84). Addition of apotransferrin to ciprofloxacin enabled a remarkable reduction in bacterial density, across a wide range of ciprofloxacin exposures. For instance, at a ciprofloxacin AUC:MIC ratio of 20, ciprofloxacin monotherapy resulted in nearly 2 log₁₀ CFU increase in bacterial density, while the combination of apotransferrin and ciprofloxacin resulted in 2 log₁₀ CFU reduction in bacterial density. Furthermore, addition of apotransferrin significantly reduced the emergence of ciprofloxacin-resistant subpopulations compared to monotherapy. These data demonstrate that decreasing the rate of bacterial replication with apotransferrin in combination with antimicrobial therapy represents an opportunity to increase the magnitude of bactericidal effect and suppress the growth rate of drug-resistant subpopulations.

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