Abstract

Antibiotic-resistant nosocomial infections are an emerging public health issue; carbapenem-resistant gram-negative bacteria such as Acinetobacter baumannii are among the pathogens against which new therapeutic agents are desperately needed. Drug repurposing has recently emerged as an alternative approach to rapidly identifying effective drugs and drug combinations to combat drug resistant bacteria. We performed a drug repurposing screen against a highly virulent, multidrug resistant, Acinetobacter baumannii strain AB5075. This strain, isolated from a patient, is resistant to 25 first-line antibiotics for gram-negative bacteria. A compound screen using a bacterial growth assay led to identification and confirmation of 43 active compounds. Among these confirmed compounds, seven are approved drugs or pharmacologically active compounds for non-antimicrobial indications. Three of these drugs, 5-fluorouracil, fluspirilene, and Bay 11-7082 resensitized strain AB5075 to azithromycin and colistin in a two-drug combination format. The approach using a drug repurposing screen with a pathogen sample isolated from a patient and a high throughput bacterial growth assay led to the successful identification of new drug combinations to overcome a multidrug resistant bacterial infection.

Highlights

  • The emergence and dissemination of drug-resistant bacterial infections are a public health issue

  • As suggested by the antimicrobial susceptibility testing guideline for Acinetobacter spp. from the Clinical and Laboratory Standards Institute (CLSI), experimental endpoints were setting at 22–24 h for the following studies

  • We describe the optimization and validation of a high throughput growth assay to measure the viability of a multidrug resistant Acinetobacter baumannii strain, Acinetobacter baumannii 5075 (AB5075)

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Summary

Introduction

The emergence and dissemination of drug-resistant bacterial infections are a public health issue. Acinetobacter baumannii is one of the major causes for the nosocomial infections in critically ill patients. Treatment of Acinetobacter baumannii can be extremely difficult, especially for the carbapenem resistant strains. Colistin and tigecycline are the last resorts for carbapenem resistant Acinetobacter baumannii. Colistin and tigecycline resistant strains have been reported worldwide (Deng et al, 2014; Oikonomou et al, 2015). In light of the rapid expansion of imipenem resistance in 35 countries, increasing from 24 to 74% in just 11 years (Xie et al, 2018), the development of novel drugs to combat Acinetobacter baumannii infections is an urgent need

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