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Amikacin potentiator activity of zinc complexed to a pyrithione derivative with enhanced solubility
Resistance to amikacin in Gram-negatives is usually mediated by the 6'-N-acetyltransferase type Ib [AAC(6')-Ib], which catalyzes the transfer of an acetyl group from acetyl CoA to the 6' position of the antibiotic molecule. A path to continue the effective use of amikacin against resi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741805/ https://www.ncbi.nlm.nih.gov/pubmed/34997203 http://dx.doi.org/10.1038/s41598-021-04724-4 |
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author | Magallon, Jesus Vu, Peter Reeves, Craig Kwan, Stella Phan, Kimberly Oakley-Havens, Crista L. Rocha, Kenneth Jimenez, Veronica Ramirez, María Soledad Tolmasky, Marcelo E. |
author_facet | Magallon, Jesus Vu, Peter Reeves, Craig Kwan, Stella Phan, Kimberly Oakley-Havens, Crista L. Rocha, Kenneth Jimenez, Veronica Ramirez, María Soledad Tolmasky, Marcelo E. |
author_sort | Magallon, Jesus |
collection | PubMed |
description | Resistance to amikacin in Gram-negatives is usually mediated by the 6'-N-acetyltransferase type Ib [AAC(6')-Ib], which catalyzes the transfer of an acetyl group from acetyl CoA to the 6' position of the antibiotic molecule. A path to continue the effective use of amikacin against resistant infections is to combine it with inhibitors of the inactivating reaction. We have recently observed that addition of Zn(2+) to in-vitro enzymatic reactions, obliterates acetylation of the acceptor antibiotic. Furthermore, when added to amikacin-containing culture medium in complex to ionophores such as pyrithione (ZnPT), it prevents the growth of resistant strains. An undesired property of ZnPT is its poor water-solubility, a problem that currently affects a large percentage of newly designed drugs. Water-solubility helps drugs to dissolve in body fluids and be transported to the target location. We tested a pyrithione derivative described previously (Magda et al. Cancer Res 68:5318–5325, 2008) that contains the amphoteric group di(ethyleneglycol)-methyl ether at position 5 (compound 5002), a modification that enhances the solubility. Compound 5002 in complex with zinc (Zn5002) was tested to assess growth inhibition of amikacin-resistant Acinetobacter baumannii and Klebsiella pneumoniae strains in the presence of the antibiotic. Zn5002 complexes in combination with amikacin at different concentrations completely inhibited growth of the tested strains. However, the concentrations needed to achieve growth inhibition were higher than those required to achieve the same results using ZnPT. Time-kill assays showed that the effect of the combination amikacin/Zn5002 was bactericidal. These results indicate that derivatives of pyrithione with enhanced water-solubility, a property that would make them drugs with better bioavailability and absorption, are a viable option for designing inhibitors of the resistance to amikacin mediated by AAC(6')-Ib, an enzyme commonly found in the clinics. |
format | Online Article Text |
id | pubmed-8741805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87418052022-01-10 Amikacin potentiator activity of zinc complexed to a pyrithione derivative with enhanced solubility Magallon, Jesus Vu, Peter Reeves, Craig Kwan, Stella Phan, Kimberly Oakley-Havens, Crista L. Rocha, Kenneth Jimenez, Veronica Ramirez, María Soledad Tolmasky, Marcelo E. Sci Rep Article Resistance to amikacin in Gram-negatives is usually mediated by the 6'-N-acetyltransferase type Ib [AAC(6')-Ib], which catalyzes the transfer of an acetyl group from acetyl CoA to the 6' position of the antibiotic molecule. A path to continue the effective use of amikacin against resistant infections is to combine it with inhibitors of the inactivating reaction. We have recently observed that addition of Zn(2+) to in-vitro enzymatic reactions, obliterates acetylation of the acceptor antibiotic. Furthermore, when added to amikacin-containing culture medium in complex to ionophores such as pyrithione (ZnPT), it prevents the growth of resistant strains. An undesired property of ZnPT is its poor water-solubility, a problem that currently affects a large percentage of newly designed drugs. Water-solubility helps drugs to dissolve in body fluids and be transported to the target location. We tested a pyrithione derivative described previously (Magda et al. Cancer Res 68:5318–5325, 2008) that contains the amphoteric group di(ethyleneglycol)-methyl ether at position 5 (compound 5002), a modification that enhances the solubility. Compound 5002 in complex with zinc (Zn5002) was tested to assess growth inhibition of amikacin-resistant Acinetobacter baumannii and Klebsiella pneumoniae strains in the presence of the antibiotic. Zn5002 complexes in combination with amikacin at different concentrations completely inhibited growth of the tested strains. However, the concentrations needed to achieve growth inhibition were higher than those required to achieve the same results using ZnPT. Time-kill assays showed that the effect of the combination amikacin/Zn5002 was bactericidal. These results indicate that derivatives of pyrithione with enhanced water-solubility, a property that would make them drugs with better bioavailability and absorption, are a viable option for designing inhibitors of the resistance to amikacin mediated by AAC(6')-Ib, an enzyme commonly found in the clinics. Nature Publishing Group UK 2022-01-07 /pmc/articles/PMC8741805/ /pubmed/34997203 http://dx.doi.org/10.1038/s41598-021-04724-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Magallon, Jesus Vu, Peter Reeves, Craig Kwan, Stella Phan, Kimberly Oakley-Havens, Crista L. Rocha, Kenneth Jimenez, Veronica Ramirez, María Soledad Tolmasky, Marcelo E. Amikacin potentiator activity of zinc complexed to a pyrithione derivative with enhanced solubility |
title | Amikacin potentiator activity of zinc complexed to a pyrithione derivative with enhanced solubility |
title_full | Amikacin potentiator activity of zinc complexed to a pyrithione derivative with enhanced solubility |
title_fullStr | Amikacin potentiator activity of zinc complexed to a pyrithione derivative with enhanced solubility |
title_full_unstemmed | Amikacin potentiator activity of zinc complexed to a pyrithione derivative with enhanced solubility |
title_short | Amikacin potentiator activity of zinc complexed to a pyrithione derivative with enhanced solubility |
title_sort | amikacin potentiator activity of zinc complexed to a pyrithione derivative with enhanced solubility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741805/ https://www.ncbi.nlm.nih.gov/pubmed/34997203 http://dx.doi.org/10.1038/s41598-021-04724-4 |
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