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SK-03-92 Drug Kills Intracellular Mycobacterium tuberculosis

Background: Tuberculosis affects millions of people worldwide. The emergence of drug-resistant Mycobacterium tuberculosis strains has made treatment more difficult. A drug discovery project initiated to screen natural products identified a lead stilbene compound, and structure function analysis of h...

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Autor principal: Schwan, William R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525840/
https://www.ncbi.nlm.nih.gov/pubmed/37760682
http://dx.doi.org/10.3390/antibiotics12091385
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author Schwan, William R.
author_facet Schwan, William R.
author_sort Schwan, William R.
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description Background: Tuberculosis affects millions of people worldwide. The emergence of drug-resistant Mycobacterium tuberculosis strains has made treatment more difficult. A drug discovery project initiated to screen natural products identified a lead stilbene compound, and structure function analysis of hundreds of analogs led to the discovery of the SK-03-92 stilbene lead compound with activity against several non-tuberculoid mycobacteria. Methods: For this study, an MIC analysis and intracellular killing assay were performed to test SK-03-92 against M. tuberculosis grown in vitro as well as within murine macrophage cells. Results: The MIC analysis showed that SK-03-92 had activity against M. tuberculosis in the range of 0.39 to 6.25 μg/mL, including activity against single-drug-resistant strains. Further, an intracellular kill assay demonstrated that the SK-03-92 lead compound killed M. tuberculosis cells within murine macrophage cells. Conclusion: Together, the data show the SK-03-92 lead compound can kill M. tuberculosis bacteria within mammalian macrophages.
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spelling pubmed-105258402023-09-28 SK-03-92 Drug Kills Intracellular Mycobacterium tuberculosis Schwan, William R. Antibiotics (Basel) Communication Background: Tuberculosis affects millions of people worldwide. The emergence of drug-resistant Mycobacterium tuberculosis strains has made treatment more difficult. A drug discovery project initiated to screen natural products identified a lead stilbene compound, and structure function analysis of hundreds of analogs led to the discovery of the SK-03-92 stilbene lead compound with activity against several non-tuberculoid mycobacteria. Methods: For this study, an MIC analysis and intracellular killing assay were performed to test SK-03-92 against M. tuberculosis grown in vitro as well as within murine macrophage cells. Results: The MIC analysis showed that SK-03-92 had activity against M. tuberculosis in the range of 0.39 to 6.25 μg/mL, including activity against single-drug-resistant strains. Further, an intracellular kill assay demonstrated that the SK-03-92 lead compound killed M. tuberculosis cells within murine macrophage cells. Conclusion: Together, the data show the SK-03-92 lead compound can kill M. tuberculosis bacteria within mammalian macrophages. MDPI 2023-08-30 /pmc/articles/PMC10525840/ /pubmed/37760682 http://dx.doi.org/10.3390/antibiotics12091385 Text en © 2023 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Schwan, William R.
SK-03-92 Drug Kills Intracellular Mycobacterium tuberculosis
title SK-03-92 Drug Kills Intracellular Mycobacterium tuberculosis
title_full SK-03-92 Drug Kills Intracellular Mycobacterium tuberculosis
title_fullStr SK-03-92 Drug Kills Intracellular Mycobacterium tuberculosis
title_full_unstemmed SK-03-92 Drug Kills Intracellular Mycobacterium tuberculosis
title_short SK-03-92 Drug Kills Intracellular Mycobacterium tuberculosis
title_sort sk-03-92 drug kills intracellular mycobacterium tuberculosis
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525840/
https://www.ncbi.nlm.nih.gov/pubmed/37760682
http://dx.doi.org/10.3390/antibiotics12091385
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