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Thiol-Containing Metallo-β-Lactamase Inhibitors Resensitize Resistant Gram-Negative Bacteria to Meropenem
[Image: see text] The prevalence of infections caused by metallo-β-lactamase (MBL) expressing Gram-negative bacteria has grown at an alarming rate in recent years. Despite the fact that MBLs can deactivate virtually all β-lactam antibiotics, there are as of yet no approved drugs available that inhib...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644712/ https://www.ncbi.nlm.nih.gov/pubmed/28820574 http://dx.doi.org/10.1021/acsinfecdis.7b00094 |
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author | Tehrani, Kamaleddin Haj Mohammad Ebrahim Martin, Nathaniel I. |
author_facet | Tehrani, Kamaleddin Haj Mohammad Ebrahim Martin, Nathaniel I. |
author_sort | Tehrani, Kamaleddin Haj Mohammad Ebrahim |
collection | PubMed |
description | [Image: see text] The prevalence of infections caused by metallo-β-lactamase (MBL) expressing Gram-negative bacteria has grown at an alarming rate in recent years. Despite the fact that MBLs can deactivate virtually all β-lactam antibiotics, there are as of yet no approved drugs available that inhibit their activity. We here examine the ability of previously reported thiol-based MBL inhibitors to synergize with meropenem and cefoperazone against a panel of Gram-negative carbapenem-resistant isolates expressing different β-lactamases. Among the compounds tested, thiomandelic acid 3 and 2-mercapto-3-phenylpropionic acid 4 were found to efficiently potentiate the activity of meropenem, especially against an imipenemase (IMP) producing strain of K. pneumoniae. In light of the zinc-dependent hydrolytic mechanism employed by MBLs, biophysical studies using isothermal titration calorimetry were also performed, revealing a correlation between the synergistic activity of thiols 3 and 4 and their zinc-binding ability with measured K(d) values of 9.8 and 20.0 μM, respectively. |
format | Online Article Text |
id | pubmed-5644712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56447122017-10-19 Thiol-Containing Metallo-β-Lactamase Inhibitors Resensitize Resistant Gram-Negative Bacteria to Meropenem Tehrani, Kamaleddin Haj Mohammad Ebrahim Martin, Nathaniel I. ACS Infect Dis [Image: see text] The prevalence of infections caused by metallo-β-lactamase (MBL) expressing Gram-negative bacteria has grown at an alarming rate in recent years. Despite the fact that MBLs can deactivate virtually all β-lactam antibiotics, there are as of yet no approved drugs available that inhibit their activity. We here examine the ability of previously reported thiol-based MBL inhibitors to synergize with meropenem and cefoperazone against a panel of Gram-negative carbapenem-resistant isolates expressing different β-lactamases. Among the compounds tested, thiomandelic acid 3 and 2-mercapto-3-phenylpropionic acid 4 were found to efficiently potentiate the activity of meropenem, especially against an imipenemase (IMP) producing strain of K. pneumoniae. In light of the zinc-dependent hydrolytic mechanism employed by MBLs, biophysical studies using isothermal titration calorimetry were also performed, revealing a correlation between the synergistic activity of thiols 3 and 4 and their zinc-binding ability with measured K(d) values of 9.8 and 20.0 μM, respectively. American Chemical Society 2017-08-18 2017-10-13 /pmc/articles/PMC5644712/ /pubmed/28820574 http://dx.doi.org/10.1021/acsinfecdis.7b00094 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Tehrani, Kamaleddin Haj Mohammad Ebrahim Martin, Nathaniel I. Thiol-Containing Metallo-β-Lactamase Inhibitors Resensitize Resistant Gram-Negative Bacteria to Meropenem |
title | Thiol-Containing Metallo-β-Lactamase Inhibitors
Resensitize Resistant Gram-Negative Bacteria to Meropenem |
title_full | Thiol-Containing Metallo-β-Lactamase Inhibitors
Resensitize Resistant Gram-Negative Bacteria to Meropenem |
title_fullStr | Thiol-Containing Metallo-β-Lactamase Inhibitors
Resensitize Resistant Gram-Negative Bacteria to Meropenem |
title_full_unstemmed | Thiol-Containing Metallo-β-Lactamase Inhibitors
Resensitize Resistant Gram-Negative Bacteria to Meropenem |
title_short | Thiol-Containing Metallo-β-Lactamase Inhibitors
Resensitize Resistant Gram-Negative Bacteria to Meropenem |
title_sort | thiol-containing metallo-β-lactamase inhibitors
resensitize resistant gram-negative bacteria to meropenem |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644712/ https://www.ncbi.nlm.nih.gov/pubmed/28820574 http://dx.doi.org/10.1021/acsinfecdis.7b00094 |
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