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Activating a Silver Lipoate Nanocluster with a Penicillin Backbone Induces a Synergistic Effect against S. aureus Biofilm
[Image: see text] Many antibiotic resistances to penicillin have been reported, making them obsolete against multiresistant bacteria. Because penicillins act by inhibiting cell wall production while silver particles disrupt the cell wall directly, a synergetic effect is anticipated when both modes o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933807/ https://www.ncbi.nlm.nih.gov/pubmed/31891070 http://dx.doi.org/10.1021/acsomega.9b02908 |
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author | Lara, Humberto H. Black, David M. Moon, Christine Orr, Elizabeth Lopez, Priscilla Alvarez, Marcos M. Baghdasarian, Glen Lopez-Ribot, Jose Whetten, Robert L. |
author_facet | Lara, Humberto H. Black, David M. Moon, Christine Orr, Elizabeth Lopez, Priscilla Alvarez, Marcos M. Baghdasarian, Glen Lopez-Ribot, Jose Whetten, Robert L. |
author_sort | Lara, Humberto H. |
collection | PubMed |
description | [Image: see text] Many antibiotic resistances to penicillin have been reported, making them obsolete against multiresistant bacteria. Because penicillins act by inhibiting cell wall production while silver particles disrupt the cell wall directly, a synergetic effect is anticipated when both modes of action are incorporated into a chimera cluster. To test this hypothesis, the lipoate ligands (LA) of a silver cluster (Ag(29)) of known composition (Ag(29)LA(12))([3−]) were covalently conjugated to 6-aminopenicillanic acid, a molecule with a β-lactam backbone. Indeed, the partially conjugated cluster inhibited an Staphylococcus aureus biofilm, in a dose–response manner, with a half-maximal inhibitory concentration IC(50) of 2.3 μM, an improvement over 60 times relative to the unconjugated cluster (IC(50) = 140 μM). An enhancement of several orders of magnitude over 6-APA alone (unconjugated) was calculated (IC(50) = 10 000 μM). Cell wall damage is documented via scanning electron microscopy. A synergistic effect of the conjugate was calculated by the combination index method described by Chou–Talalay. This hybrid nanoantibiotic opens a new front against multidrug-resistant pathogens. |
format | Online Article Text |
id | pubmed-6933807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-69338072019-12-30 Activating a Silver Lipoate Nanocluster with a Penicillin Backbone Induces a Synergistic Effect against S. aureus Biofilm Lara, Humberto H. Black, David M. Moon, Christine Orr, Elizabeth Lopez, Priscilla Alvarez, Marcos M. Baghdasarian, Glen Lopez-Ribot, Jose Whetten, Robert L. ACS Omega [Image: see text] Many antibiotic resistances to penicillin have been reported, making them obsolete against multiresistant bacteria. Because penicillins act by inhibiting cell wall production while silver particles disrupt the cell wall directly, a synergetic effect is anticipated when both modes of action are incorporated into a chimera cluster. To test this hypothesis, the lipoate ligands (LA) of a silver cluster (Ag(29)) of known composition (Ag(29)LA(12))([3−]) were covalently conjugated to 6-aminopenicillanic acid, a molecule with a β-lactam backbone. Indeed, the partially conjugated cluster inhibited an Staphylococcus aureus biofilm, in a dose–response manner, with a half-maximal inhibitory concentration IC(50) of 2.3 μM, an improvement over 60 times relative to the unconjugated cluster (IC(50) = 140 μM). An enhancement of several orders of magnitude over 6-APA alone (unconjugated) was calculated (IC(50) = 10 000 μM). Cell wall damage is documented via scanning electron microscopy. A synergistic effect of the conjugate was calculated by the combination index method described by Chou–Talalay. This hybrid nanoantibiotic opens a new front against multidrug-resistant pathogens. American Chemical Society 2019-12-13 /pmc/articles/PMC6933807/ /pubmed/31891070 http://dx.doi.org/10.1021/acsomega.9b02908 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Lara, Humberto H. Black, David M. Moon, Christine Orr, Elizabeth Lopez, Priscilla Alvarez, Marcos M. Baghdasarian, Glen Lopez-Ribot, Jose Whetten, Robert L. Activating a Silver Lipoate Nanocluster with a Penicillin Backbone Induces a Synergistic Effect against S. aureus Biofilm |
title | Activating a Silver
Lipoate Nanocluster with a Penicillin
Backbone Induces a Synergistic Effect against S. aureus Biofilm |
title_full | Activating a Silver
Lipoate Nanocluster with a Penicillin
Backbone Induces a Synergistic Effect against S. aureus Biofilm |
title_fullStr | Activating a Silver
Lipoate Nanocluster with a Penicillin
Backbone Induces a Synergistic Effect against S. aureus Biofilm |
title_full_unstemmed | Activating a Silver
Lipoate Nanocluster with a Penicillin
Backbone Induces a Synergistic Effect against S. aureus Biofilm |
title_short | Activating a Silver
Lipoate Nanocluster with a Penicillin
Backbone Induces a Synergistic Effect against S. aureus Biofilm |
title_sort | activating a silver
lipoate nanocluster with a penicillin
backbone induces a synergistic effect against s. aureus biofilm |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933807/ https://www.ncbi.nlm.nih.gov/pubmed/31891070 http://dx.doi.org/10.1021/acsomega.9b02908 |
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