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A Macromolecule Reversing Antibiotic Resistance Phenotype and Repurposing Drugs as Potent Antibiotics.

Xin DingChuan YangWilfried MoreiraPeiyan YuanBalamurugan PeriaswamyPaola Florez de SessionsHuimin ZhaoJeremy TanAshlynn LeeKai Xun OngNathaniel ParkZhen Chang LiangJames L HedrickYi Yan Yang
Published in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2020)
In order to mitigate antibiotic resistance, a new strategy to increase antibiotic potency and reverse drug resistance is needed. Herein, the translocation mechanism of an antimicrobial guanidinium-functionalized polycarbonate is leveraged in combination with traditional antibiotics to afford a potent treatment for drug-resistant bacteria. Particularly, this polymer-antibiotic combination approach reverses rifampicin resistance phenotype in Acinetobacter baumannii demonstrating a 2.5 × 105-fold reduction in minimum inhibitory concentration (MIC) and a 4096-fold reduction in minimum bactericidal concentration (MBC). This approach also enables the repurposing of auranofin as an antibiotic against multidrug-resistant (MDR) Gram-negative bacteria with a 512-fold MIC and 128-fold MBC reduction, respectively. Finally, the in vivo efficacy of polymer-rifampicin combination is demonstrated in a MDR bacteremia mouse model. This combination approach lays foundational ground rules for a new class of antibiotic adjuvants capable of reversing drug resistance phenotype and repurposing drugs against MDR Gram-negative bacteria.
Keyphrases
  • multidrug resistant
  • drug resistant
  • acinetobacter baumannii
  • gram negative
  • klebsiella pneumoniae
  • mouse model
  • staphylococcus aureus
  • pseudomonas aeruginosa
  • molecularly imprinted
  • simultaneous determination