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Auranofin derivatives as potent bactericidal antimicrobials against cystic fibrosis pathogen Burkholderia cenocepacia
* 1 , 2 , 2 , 2 , 2 , 1
1  University of Manitoba
2  University of Massachusetts Lowell

Published: 26 April 2021 by MDPI in The 1st International Electronic Conference on Antibiotics session Poster (registering DOI)

The Burkholderia cepacia complex (Bcc), is a group of closely related bacterial pathogens which commonly infects people with the genetic disease cystic fibrosis. Bcc infections cause a severe drop in lung function and cepacia syndrome, a life-threatening type of sepsis. A species of the Bcc, Burkholderia cenocepacia is inherently resistant to many of the antibiotics currently used in the clinics, leading to persistent infections. One way of developing novel antibiotics is to repurpose approved drugs and develop them as antimicrobials. One example is auranofin; however, auranofin is inactive in many Gram-negative bacteria, possibly due to the presence of the highly impermeable outer membrane. We hypothesized that derivatives of auranofin could inhibit the growth of the multidrug resistant pathogen B. cenocepacia and these compounds could be possible candidates for further drug development. We have found two auranofin derivatives that are potent against B. cenocepacia and are comparable in activity to clinical antibiotics. The auranofin derivatives are bactericidal to both exponential and stationary phase cells and have lower minimum inhibitory concentrations (MICs) than clinical antibiotics. Further, these compounds can also kill persister cells created by other antibiotics. A continuously growing culture exposed to the drugs did not develop spontaneous resistance over the course of 24 days, showing resistance will not be easy to generate. Thus, the two auranofin derivatives have ideal characteristics to be further developed into antimicrobials to clear B. cenocepacia lung infections in cystic fibrosis patients.

Keywords: Antimicrobials; Burkholderia; cystic fibrosis; auranofin