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Nickel chelation therapy as an approach to combat multi-drug resistant enteric pathogens
The nickel (Ni)-specific chelator dimethylglyoxime (DMG) has been used for many years to detect, quantitate or decrease Ni levels in various environments. Addition of DMG at millimolar levels has a bacteriostatic effect on some enteric pathogens, including multidrug resistant (MDR) strains of Salmon...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761267/ https://www.ncbi.nlm.nih.gov/pubmed/31554822 http://dx.doi.org/10.1038/s41598-019-50027-0 |
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author | Benoit, Stéphane L. Schmalstig, Alan A. Glushka, John Maier, Susan E. Edison, Arthur S. Maier, Robert J. |
author_facet | Benoit, Stéphane L. Schmalstig, Alan A. Glushka, John Maier, Susan E. Edison, Arthur S. Maier, Robert J. |
author_sort | Benoit, Stéphane L. |
collection | PubMed |
description | The nickel (Ni)-specific chelator dimethylglyoxime (DMG) has been used for many years to detect, quantitate or decrease Ni levels in various environments. Addition of DMG at millimolar levels has a bacteriostatic effect on some enteric pathogens, including multidrug resistant (MDR) strains of Salmonella Typhimurium and Klebsiella pneumoniae. DMG inhibited activity of two Ni-containing enzymes, Salmonella hydrogenase and Klebsiella urease. Oral delivery of nontoxic levels of DMG to mice previously inoculated with S. Typhimurium led to a 50% survival rate, while 100% of infected mice in the no-DMG control group succumbed to salmonellosis. Pathogen colonization numbers from livers and spleens of mice were 10- fold reduced by DMG treatment of the Salmonella-infected mice. Using Nuclear Magnetic Resonance, we were able to detect DMG in the livers of DMG-(orally) treated mice. Inoculation of Galleria mellonella (wax moth) larvae with DMG prior to injection of either MDR K. pneumoniae or MDR S. Typhimurium led to 40% and 60% survival, respectively, compared to 100% mortality of larvae infected with either pathogen, but without prior DMG administration. Our results suggest that DMG-mediated Ni-chelation could provide a novel approach to combat enteric pathogens, including recalcitrant multi-drug resistant strains. |
format | Online Article Text |
id | pubmed-6761267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67612672019-10-02 Nickel chelation therapy as an approach to combat multi-drug resistant enteric pathogens Benoit, Stéphane L. Schmalstig, Alan A. Glushka, John Maier, Susan E. Edison, Arthur S. Maier, Robert J. Sci Rep Article The nickel (Ni)-specific chelator dimethylglyoxime (DMG) has been used for many years to detect, quantitate or decrease Ni levels in various environments. Addition of DMG at millimolar levels has a bacteriostatic effect on some enteric pathogens, including multidrug resistant (MDR) strains of Salmonella Typhimurium and Klebsiella pneumoniae. DMG inhibited activity of two Ni-containing enzymes, Salmonella hydrogenase and Klebsiella urease. Oral delivery of nontoxic levels of DMG to mice previously inoculated with S. Typhimurium led to a 50% survival rate, while 100% of infected mice in the no-DMG control group succumbed to salmonellosis. Pathogen colonization numbers from livers and spleens of mice were 10- fold reduced by DMG treatment of the Salmonella-infected mice. Using Nuclear Magnetic Resonance, we were able to detect DMG in the livers of DMG-(orally) treated mice. Inoculation of Galleria mellonella (wax moth) larvae with DMG prior to injection of either MDR K. pneumoniae or MDR S. Typhimurium led to 40% and 60% survival, respectively, compared to 100% mortality of larvae infected with either pathogen, but without prior DMG administration. Our results suggest that DMG-mediated Ni-chelation could provide a novel approach to combat enteric pathogens, including recalcitrant multi-drug resistant strains. Nature Publishing Group UK 2019-09-25 /pmc/articles/PMC6761267/ /pubmed/31554822 http://dx.doi.org/10.1038/s41598-019-50027-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Benoit, Stéphane L. Schmalstig, Alan A. Glushka, John Maier, Susan E. Edison, Arthur S. Maier, Robert J. Nickel chelation therapy as an approach to combat multi-drug resistant enteric pathogens |
title | Nickel chelation therapy as an approach to combat multi-drug resistant enteric pathogens |
title_full | Nickel chelation therapy as an approach to combat multi-drug resistant enteric pathogens |
title_fullStr | Nickel chelation therapy as an approach to combat multi-drug resistant enteric pathogens |
title_full_unstemmed | Nickel chelation therapy as an approach to combat multi-drug resistant enteric pathogens |
title_short | Nickel chelation therapy as an approach to combat multi-drug resistant enteric pathogens |
title_sort | nickel chelation therapy as an approach to combat multi-drug resistant enteric pathogens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761267/ https://www.ncbi.nlm.nih.gov/pubmed/31554822 http://dx.doi.org/10.1038/s41598-019-50027-0 |
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