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Inhibitory Effect of Epigallocatechin Gallate-Silver Nanoparticles and Their Lysozyme Bioconjugates on Biofilm Formation and Cytotoxicity
[Image: see text] Biofilms are multicellular communities of microbial cells that grow on natural and synthetic surfaces. They have become the major cause for hospital-acquired infections because once they form, they are very difficult to eradicate. Nanotechnology offers means to fight biofilm-associ...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490750/ https://www.ncbi.nlm.nih.gov/pubmed/35977081 http://dx.doi.org/10.1021/acsabm.2c00409 |
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author | Meesaragandla, Brahmaiah Hayet, Shahar Fine, Tamir Janke, Una Chai, Liraz Delcea, Mihaela |
author_facet | Meesaragandla, Brahmaiah Hayet, Shahar Fine, Tamir Janke, Una Chai, Liraz Delcea, Mihaela |
author_sort | Meesaragandla, Brahmaiah |
collection | PubMed |
description | [Image: see text] Biofilms are multicellular communities of microbial cells that grow on natural and synthetic surfaces. They have become the major cause for hospital-acquired infections because once they form, they are very difficult to eradicate. Nanotechnology offers means to fight biofilm-associated infections. Here, we report on the synthesis of silver nanoparticles (AgNPs) with the antibacterial ligand epigallocatechin gallate (EGCG) and the formation of a lysozyme protein corona on AgNPs, as shown by UV–vis, dynamic light scattering, and circular dichroism analyses. We further tested the activity of EGCG-AgNPs and their lysozyme bioconjugates on the viability of Bacillus subtilis cells and biofilm formation. Our results showed that, although EGCG-AgNPs presented no antibacterial activity on planktonic B. subtilis cells, they inhibited B. subtilis biofilm formation at concentrations larger than 40 nM, and EGCG-AgNP-lysozyme bioconjugates inhibited biofilms at concentrations above 80 nM. Cytotoxicity assays performed with human cells showed a reverse trend, where EGCG-AgNPs barely affected human cell viability while EGCG-AgNP-lysozyme bioconjugates severely hampered viability. Our results therefore demonstrate that EGCG-AgNPs may be used as noncytotoxic antibiofilm agents. |
format | Online Article Text |
id | pubmed-9490750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94907502022-09-22 Inhibitory Effect of Epigallocatechin Gallate-Silver Nanoparticles and Their Lysozyme Bioconjugates on Biofilm Formation and Cytotoxicity Meesaragandla, Brahmaiah Hayet, Shahar Fine, Tamir Janke, Una Chai, Liraz Delcea, Mihaela ACS Appl Bio Mater [Image: see text] Biofilms are multicellular communities of microbial cells that grow on natural and synthetic surfaces. They have become the major cause for hospital-acquired infections because once they form, they are very difficult to eradicate. Nanotechnology offers means to fight biofilm-associated infections. Here, we report on the synthesis of silver nanoparticles (AgNPs) with the antibacterial ligand epigallocatechin gallate (EGCG) and the formation of a lysozyme protein corona on AgNPs, as shown by UV–vis, dynamic light scattering, and circular dichroism analyses. We further tested the activity of EGCG-AgNPs and their lysozyme bioconjugates on the viability of Bacillus subtilis cells and biofilm formation. Our results showed that, although EGCG-AgNPs presented no antibacterial activity on planktonic B. subtilis cells, they inhibited B. subtilis biofilm formation at concentrations larger than 40 nM, and EGCG-AgNP-lysozyme bioconjugates inhibited biofilms at concentrations above 80 nM. Cytotoxicity assays performed with human cells showed a reverse trend, where EGCG-AgNPs barely affected human cell viability while EGCG-AgNP-lysozyme bioconjugates severely hampered viability. Our results therefore demonstrate that EGCG-AgNPs may be used as noncytotoxic antibiofilm agents. American Chemical Society 2022-08-17 2022-09-19 /pmc/articles/PMC9490750/ /pubmed/35977081 http://dx.doi.org/10.1021/acsabm.2c00409 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Meesaragandla, Brahmaiah Hayet, Shahar Fine, Tamir Janke, Una Chai, Liraz Delcea, Mihaela Inhibitory Effect of Epigallocatechin Gallate-Silver Nanoparticles and Their Lysozyme Bioconjugates on Biofilm Formation and Cytotoxicity |
title | Inhibitory Effect
of Epigallocatechin Gallate-Silver
Nanoparticles and Their Lysozyme Bioconjugates on Biofilm Formation
and Cytotoxicity |
title_full | Inhibitory Effect
of Epigallocatechin Gallate-Silver
Nanoparticles and Their Lysozyme Bioconjugates on Biofilm Formation
and Cytotoxicity |
title_fullStr | Inhibitory Effect
of Epigallocatechin Gallate-Silver
Nanoparticles and Their Lysozyme Bioconjugates on Biofilm Formation
and Cytotoxicity |
title_full_unstemmed | Inhibitory Effect
of Epigallocatechin Gallate-Silver
Nanoparticles and Their Lysozyme Bioconjugates on Biofilm Formation
and Cytotoxicity |
title_short | Inhibitory Effect
of Epigallocatechin Gallate-Silver
Nanoparticles and Their Lysozyme Bioconjugates on Biofilm Formation
and Cytotoxicity |
title_sort | inhibitory effect
of epigallocatechin gallate-silver
nanoparticles and their lysozyme bioconjugates on biofilm formation
and cytotoxicity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490750/ https://www.ncbi.nlm.nih.gov/pubmed/35977081 http://dx.doi.org/10.1021/acsabm.2c00409 |
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