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New Auranofin Analogs with Antibacterial Properties against Burkholderia Clinical Isolates
Bacteria of the genus Burkholderia include pathogenic Burkholderia mallei, Burkholderia pseudomallei and the Burkholderia cepacia complex (Bcc). These Gram-negative pathogens have intrinsic drug resistance, which makes treatment of infections difficult. Bcc affects individuals with cystic fibrosis (...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697972/ https://www.ncbi.nlm.nih.gov/pubmed/34943654 http://dx.doi.org/10.3390/antibiotics10121443 |
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author | Maydaniuk, Dustin Wu, Bin Truong, Dang Liyanage, Sajani H. Hogan, Andrew M. Yap, Zhong Ling Yan, Mingdi Cardona, Silvia T. |
author_facet | Maydaniuk, Dustin Wu, Bin Truong, Dang Liyanage, Sajani H. Hogan, Andrew M. Yap, Zhong Ling Yan, Mingdi Cardona, Silvia T. |
author_sort | Maydaniuk, Dustin |
collection | PubMed |
description | Bacteria of the genus Burkholderia include pathogenic Burkholderia mallei, Burkholderia pseudomallei and the Burkholderia cepacia complex (Bcc). These Gram-negative pathogens have intrinsic drug resistance, which makes treatment of infections difficult. Bcc affects individuals with cystic fibrosis (CF) and the species B. cenocepacia is associated with one of the worst clinical outcomes. Following the repurposing of auranofin as an antibacterial against Gram-positive bacteria, we previously synthetized auranofin analogs with activity against Gram-negatives. In this work, we show that two auranofin analogs, MS-40S and MS-40, have antibiotic activity against Burkholderia clinical isolates. The compounds are bactericidal against B. cenocepacia and kill stationary-phase cells and persisters without selecting for multistep resistance. Caenorhabditis elegans and Galleria mellonella tolerated high concentrations of MS-40S and MS-40, demonstrating that these compounds have low toxicity in these model organisms. In summary, we show that MS-40 and MS-40S have antimicrobial properties that warrant further investigations to determine their therapeutic potential against Burkholderia infections. |
format | Online Article Text |
id | pubmed-8697972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86979722021-12-24 New Auranofin Analogs with Antibacterial Properties against Burkholderia Clinical Isolates Maydaniuk, Dustin Wu, Bin Truong, Dang Liyanage, Sajani H. Hogan, Andrew M. Yap, Zhong Ling Yan, Mingdi Cardona, Silvia T. Antibiotics (Basel) Article Bacteria of the genus Burkholderia include pathogenic Burkholderia mallei, Burkholderia pseudomallei and the Burkholderia cepacia complex (Bcc). These Gram-negative pathogens have intrinsic drug resistance, which makes treatment of infections difficult. Bcc affects individuals with cystic fibrosis (CF) and the species B. cenocepacia is associated with one of the worst clinical outcomes. Following the repurposing of auranofin as an antibacterial against Gram-positive bacteria, we previously synthetized auranofin analogs with activity against Gram-negatives. In this work, we show that two auranofin analogs, MS-40S and MS-40, have antibiotic activity against Burkholderia clinical isolates. The compounds are bactericidal against B. cenocepacia and kill stationary-phase cells and persisters without selecting for multistep resistance. Caenorhabditis elegans and Galleria mellonella tolerated high concentrations of MS-40S and MS-40, demonstrating that these compounds have low toxicity in these model organisms. In summary, we show that MS-40 and MS-40S have antimicrobial properties that warrant further investigations to determine their therapeutic potential against Burkholderia infections. MDPI 2021-11-24 /pmc/articles/PMC8697972/ /pubmed/34943654 http://dx.doi.org/10.3390/antibiotics10121443 Text en © 2021 by the authors. 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 | Article Maydaniuk, Dustin Wu, Bin Truong, Dang Liyanage, Sajani H. Hogan, Andrew M. Yap, Zhong Ling Yan, Mingdi Cardona, Silvia T. New Auranofin Analogs with Antibacterial Properties against Burkholderia Clinical Isolates |
title | New Auranofin Analogs with Antibacterial Properties against Burkholderia Clinical Isolates |
title_full | New Auranofin Analogs with Antibacterial Properties against Burkholderia Clinical Isolates |
title_fullStr | New Auranofin Analogs with Antibacterial Properties against Burkholderia Clinical Isolates |
title_full_unstemmed | New Auranofin Analogs with Antibacterial Properties against Burkholderia Clinical Isolates |
title_short | New Auranofin Analogs with Antibacterial Properties against Burkholderia Clinical Isolates |
title_sort | new auranofin analogs with antibacterial properties against burkholderia clinical isolates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697972/ https://www.ncbi.nlm.nih.gov/pubmed/34943654 http://dx.doi.org/10.3390/antibiotics10121443 |
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