Serendipitous Discovery of a Highly Active and Selective Resistance-Modifying Agent for Colistin-Resistant Gram-Negative Bacteria.

Yuefeng Gao, Somnath Dutta, Xiang Wang
Author Information
  1. Yuefeng Gao: Department of Chemistry, University of Colorado, Boulder, Colorado 80309, United States. ORCID
  2. Somnath Dutta: Department of Chemistry, University of Colorado, Boulder, Colorado 80309, United States. ORCID
  3. Xiang Wang: Department of Chemistry, University of Colorado, Boulder, Colorado 80309, United States. ORCID

Abstract

Antibiotic resistance is a growing global health concern. Colistin is one of the last-resort antibiotics that treats multidrug-resistant (MDR) Gram-negative bacterial infection. However, bacteria resistant to colistin have become increasingly prevalent. Using a bacterial whole-cell screen of a fragment-based library, one compound was discovered to resensitize MDR AR-0493 to colistin with low mammalian toxicity. Interestingly, postscreening validation studies identified a highly related yet distinct compound as the actual substance responsible for the activity. Further studies showed that this novel resistance-modifying agent is not only very potent but also highly selective to potentiate the activity of polymyxin family antibiotics in a wide range of MDR Gram-negative bacteria. Thus, it may be further developed as a combination therapy to prolong the life span of colistin in the clinic.

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Grants

  1. R33 AI121581/NIAID NIH HHS

Word Cloud

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