Journal
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume 59, Issue 8, Pages 4835-4844Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.00692-15
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Funding
- NIH [AI083632, R01-AI104499, R01-AI104952]
- University of Alabama at Birmingham (UAB) Center for AIDS Research (CFAR), an NIH [P30 AI027767]
- NIH NIAID
- NIH NIMH
- NIH NIDA
- NIH NICHD
- NIH NHLBI
- NIH NIA
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Tuberculosis is a severe disease affecting millions worldwide. Unfortunately, treatment strategies are hampered both by the prohibitively long treatment regimen and the rise of drug-resistant strains. Significant effort has been expended in the search for new treatments, but few options have successfully emerged, and new treatment modalities are desperately needed. Recently, there has been growing interest in the synergistic antibacterial effects of copper ions (Cu-II/I) in combination with certain small molecular compounds, and we have previously reported development of a drug screening strategy to harness the intrinsic bactericidal properties of Cu-II/I. Here, we describe the copper-dependent a ntimycobacterial properties of disulfiram, an FDA-approved and well-tolerated sobriety aid. Disulfiram was inhibitory to mycobacteria only in the presence of Cu-II/I and exerted its bactericidal activity well below the active concentration of Cu-II/I or disulfiram alone. No other physiologically relevant bivalent transition metals (e.g., Fe-II, Ni-II Mn-II, and Co-II) exhibited this effect. We demonstrate that the movement of the disulfiram-copper complex across the cell envelope is porin independent and can inhibit intracellular protein functions. Additionally, the complex is able to synergistically induce intracellular copper stress responses significantly more than Cu-II/I alone. Our data suggest that by complexing with disulfiram, Cu-II/I is likely allowed unfettered access to vulnerable intracellular components, bypassing the normally sufficient copper homeostatic machinery. Overall, the synergistic antibacterial activity of Cu-II/I and disulfiram reveals the susceptibility of the copper homeostasis system of Mycobacterium tuberculosis to chemical attacks and establishes compounds that act in concert with copper as a new class of bacterial inhibitors.
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