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Five nanometer size highly positive silver nanoparticles are bactericidal targeting cell wall and adherent fimbriae expression

To tackle growing antibiotic resistance (AR) and hospital-acquired infections (HAIs), novel antimicrobials are warranted that are effective against HAIs and safer for human use. We hypothesize that small 5 nm size positively charged nanoparticles could specifically target bacterial cell wall and adh...

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Autores principales: Pokhrel, Lok R., Jacobs, Zachary L., Dikin, Dmitriy, Akula, Shaw M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039075/
https://www.ncbi.nlm.nih.gov/pubmed/35468937
http://dx.doi.org/10.1038/s41598-022-10778-9
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author Pokhrel, Lok R.
Jacobs, Zachary L.
Dikin, Dmitriy
Akula, Shaw M.
author_facet Pokhrel, Lok R.
Jacobs, Zachary L.
Dikin, Dmitriy
Akula, Shaw M.
author_sort Pokhrel, Lok R.
collection PubMed
description To tackle growing antibiotic resistance (AR) and hospital-acquired infections (HAIs), novel antimicrobials are warranted that are effective against HAIs and safer for human use. We hypothesize that small 5 nm size positively charged nanoparticles could specifically target bacterial cell wall and adherent fimbriae expression, serving as the next generation antibacterial agent. Herein we show highly positively charged, 5 nm amino-functionalized silver nanoparticles (NH(2)–AgNPs) were bactericidal; highly negatively charged, 45 nm citrate-functionalized AgNPs (Citrate–AgNPs) were nontoxic; and Ag(+) ions were bacteriostatic forming honeycomb-like potentially resistant phenotype, at 10 µg Ag/mL in E. coli. Further, adherent fimbriae were expressed with Citrate–AgNPs (0.5–10 µg/mL), whereas NH(2)–AgNPs (0.5–10 µg/mL) or Ag(+) ions (only at 10 µg/mL) inhibited fimbriae expression. Our results also showed no lipid peroxidation in human lung epithelial and dermal fibroblast cells upon NH(2)–AgNPs treatments, suggesting NH(2)–AgNPs as a biocompatible antibacterial candidate. Potent bactericidal effects demonstrated by biocompatible NH(2)–AgNPs and the lack of toxicity of Citrate–AgNPs lend credence to the hypothesis that small size, positively charged AgNPs may serve as a next-generation antibacterial agent, potentially addressing the rising HAIs and patient health and safety.
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spelling pubmed-90390752022-04-27 Five nanometer size highly positive silver nanoparticles are bactericidal targeting cell wall and adherent fimbriae expression Pokhrel, Lok R. Jacobs, Zachary L. Dikin, Dmitriy Akula, Shaw M. Sci Rep Article To tackle growing antibiotic resistance (AR) and hospital-acquired infections (HAIs), novel antimicrobials are warranted that are effective against HAIs and safer for human use. We hypothesize that small 5 nm size positively charged nanoparticles could specifically target bacterial cell wall and adherent fimbriae expression, serving as the next generation antibacterial agent. Herein we show highly positively charged, 5 nm amino-functionalized silver nanoparticles (NH(2)–AgNPs) were bactericidal; highly negatively charged, 45 nm citrate-functionalized AgNPs (Citrate–AgNPs) were nontoxic; and Ag(+) ions were bacteriostatic forming honeycomb-like potentially resistant phenotype, at 10 µg Ag/mL in E. coli. Further, adherent fimbriae were expressed with Citrate–AgNPs (0.5–10 µg/mL), whereas NH(2)–AgNPs (0.5–10 µg/mL) or Ag(+) ions (only at 10 µg/mL) inhibited fimbriae expression. Our results also showed no lipid peroxidation in human lung epithelial and dermal fibroblast cells upon NH(2)–AgNPs treatments, suggesting NH(2)–AgNPs as a biocompatible antibacterial candidate. Potent bactericidal effects demonstrated by biocompatible NH(2)–AgNPs and the lack of toxicity of Citrate–AgNPs lend credence to the hypothesis that small size, positively charged AgNPs may serve as a next-generation antibacterial agent, potentially addressing the rising HAIs and patient health and safety. Nature Publishing Group UK 2022-04-25 /pmc/articles/PMC9039075/ /pubmed/35468937 http://dx.doi.org/10.1038/s41598-022-10778-9 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
Pokhrel, Lok R.
Jacobs, Zachary L.
Dikin, Dmitriy
Akula, Shaw M.
Five nanometer size highly positive silver nanoparticles are bactericidal targeting cell wall and adherent fimbriae expression
title Five nanometer size highly positive silver nanoparticles are bactericidal targeting cell wall and adherent fimbriae expression
title_full Five nanometer size highly positive silver nanoparticles are bactericidal targeting cell wall and adherent fimbriae expression
title_fullStr Five nanometer size highly positive silver nanoparticles are bactericidal targeting cell wall and adherent fimbriae expression
title_full_unstemmed Five nanometer size highly positive silver nanoparticles are bactericidal targeting cell wall and adherent fimbriae expression
title_short Five nanometer size highly positive silver nanoparticles are bactericidal targeting cell wall and adherent fimbriae expression
title_sort five nanometer size highly positive silver nanoparticles are bactericidal targeting cell wall and adherent fimbriae expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039075/
https://www.ncbi.nlm.nih.gov/pubmed/35468937
http://dx.doi.org/10.1038/s41598-022-10778-9
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