Evaluating New Compounds to Treat Burkholderia pseudomallei Infections

Bibliographic Details
Title: Evaluating New Compounds to Treat Burkholderia pseudomallei Infections
Authors: Brittany N. Ross, Julia N. Myers, Laura A. Muruato, Daniel Tapia, Alfredo G. Torres
Source: Frontiers in Cellular and Infection Microbiology, Vol 8 (2018)
Publisher Information: Frontiers Media S.A., 2018.
Publication Year: 2018
Collection: LCC:Microbiology
Subject Terms: Burkholderia, antibiotic resistance, persistence, pathogen box, treatment, Microbiology, QR1-502
More Details: Burkholderia pseudomallei is the causative agent of melioidosis, a disease that requires long-term treatment regimens with no assurance of bacterial clearance. Clinical isolates are intrinsically resistant to most antibiotics and in recent years, isolates have been collected that display resistance to frontline drugs. With the expanding global burden of B. pseudomallei, there is a need to identify new compounds or improve current treatments to reduce risk of relapse. Using the Pathogen Box generated by Medicines for Malaria Venture, we screened a library of 400 compounds for bacteriostatic or bactericidal activity against B. pseudomallei K96243 and identified seven compounds that exhibited inhibitory effects. New compounds found to have function against B. pseudomallei were auranofin, rifampicin, miltefosine, MMV688179, and MMV688271. An additional two compounds currently used to treat melioidosis, doxycycline and levofloxacin, were also identified in the screen. We determined that the minimal inhibitory concentrations (MIC) for levofloxacin, doxycycline, and MMV688271 were below 12 μg/ml for 5 strains of B. pseudomallei. To assess persister frequency, bacteria were exposed to 100x MIC of each compound. Auranofin, MMV688179, and MMV688271 reduced the bacterial population to an average of 4.53 × 10−6% compared to ceftazidime, which corresponds to 25.1% survival. Overall, our data demonstrates that auranofin, MMV688197, and MMV688271 have the potential to become repurposed drugs for treating melioidosis infections and the first evidence that alternative therapeutics can reduce B. pseudomallei persistence.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2235-2988
Relation: https://www.frontiersin.org/article/10.3389/fcimb.2018.00210/full; https://doaj.org/toc/2235-2988
DOI: 10.3389/fcimb.2018.00210
Access URL: https://doaj.org/article/bb85445d0678490093a0f4b64a6f2f6a
Accession Number: edsdoj.bb85445d0678490093a0f4b64a6f2f6a
Database: Directory of Open Access Journals
More Details
ISSN:22352988
DOI:10.3389/fcimb.2018.00210
Published in:Frontiers in Cellular and Infection Microbiology
Language:English