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Species differences in ciprofloxacin resistance among Gram-negative bacteria: can "anti-mutant" ratios of the area under the concentration-time curve to the MIC be achieved clinically?

Elena N StrukovaYury A PortnoyStephen H ZinnerAlexander A Firsov
Published in: Journal of chemotherapy (Florence, Italy) (2017)
To explore if the 'anti-mutant' ratios of 24-h area under the concentration-time curve (AUC24) to the MIC overlap the clinically attainable AUC24/MICs, the selection of ciprofloxacin-resistant Escherichia coli, Pseudomonas aeruginosa and Klebsiella pneumoniae mutants was studied in dynamic model that simulates human pharmacokinetics of ciprofloxacin. Four strains each of E. coli and P. aeruginosa and three strains of K. pneumoniae were exposed to ciprofloxacin over a 50-400-fold range of the AUC24/MIC ratio. Based on population analysis data, areas under the bacterial mutant concentration-time curves (AUBCMs) were determined for subpopulations resistant to 4×, 8× and 16× MIC of the antibiotic. The emergence of resistance among three Gram-negative organisms was concentration dependent. Based on the AUBCM vs. AUC24/MIC curves, the predicted 'anti-mutant' AUC24/MIC ratios were clinically attainable with E. coli but not with P. aeruginosa and K. pneumoniae. The emergence of fluoroquinolone resistance in a clinical setting can be predicted using dynamic models.
Keyphrases
  • escherichia coli
  • pseudomonas aeruginosa
  • klebsiella pneumoniae
  • gram negative
  • multidrug resistant
  • wild type
  • biofilm formation
  • cystic fibrosis
  • endothelial cells
  • drug resistant
  • big data
  • deep learning