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Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant

Silver (Ag) is known to possess antimicrobial properties which is commonly attributed to soluble Ag ions. Here, we showed that Ag nanoparticles (NPs) potently inhibited SARS-CoV-2 infection using two different pseudovirus neutralization assays. We also evaluated a set of Ag nanoparticles of differen...

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Autores principales: Gupta, Govind, Hamawandi, Bejan, Sheward, Daniel J., Murrell, Ben, Hanke, Leo, McInerney, Gerald, Blosi, Magda, Costa, Anna L., Toprak, Muhammet S., Fadeel, Bengt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790969/
https://www.ncbi.nlm.nih.gov/pubmed/36578508
http://dx.doi.org/10.3389/fbioe.2022.1083232
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author Gupta, Govind
Hamawandi, Bejan
Sheward, Daniel J.
Murrell, Ben
Hanke, Leo
McInerney, Gerald
Blosi, Magda
Costa, Anna L.
Toprak, Muhammet S.
Fadeel, Bengt
author_facet Gupta, Govind
Hamawandi, Bejan
Sheward, Daniel J.
Murrell, Ben
Hanke, Leo
McInerney, Gerald
Blosi, Magda
Costa, Anna L.
Toprak, Muhammet S.
Fadeel, Bengt
author_sort Gupta, Govind
collection PubMed
description Silver (Ag) is known to possess antimicrobial properties which is commonly attributed to soluble Ag ions. Here, we showed that Ag nanoparticles (NPs) potently inhibited SARS-CoV-2 infection using two different pseudovirus neutralization assays. We also evaluated a set of Ag nanoparticles of different sizes with varying surface properties, including polyvinylpyrrolidone (PVP)-coated and poly (ethylene glycol) (PEG)-modified Ag nanoparticles, and found that only the bare (unmodified) nanoparticles were able to prevent virus infection. For comparison, TiO(2) nanoparticles failed to intercept the virus. Proteins and lipids may adsorb to nanoparticles forming a so-called bio-corona; however, Ag nanoparticles pre-incubated with pulmonary surfactant retained their ability to block virus infection in the present model. Furthermore, the secondary structure of the spike protein of SARS-CoV-2 was perturbed by the Ag nanoparticles, but not by the ionic control (AgNO(3)) nor by the TiO(2) nanoparticles. Finally, Ag nanoparticles were shown to be non-cytotoxic towards the human lung epithelial cell line BEAS-2B and this was confirmed by using primary human nasal epithelial cells. These results further support that Ag nanoparticles may find use as anti-viral agents.
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spelling pubmed-97909692022-12-27 Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant Gupta, Govind Hamawandi, Bejan Sheward, Daniel J. Murrell, Ben Hanke, Leo McInerney, Gerald Blosi, Magda Costa, Anna L. Toprak, Muhammet S. Fadeel, Bengt Front Bioeng Biotechnol Bioengineering and Biotechnology Silver (Ag) is known to possess antimicrobial properties which is commonly attributed to soluble Ag ions. Here, we showed that Ag nanoparticles (NPs) potently inhibited SARS-CoV-2 infection using two different pseudovirus neutralization assays. We also evaluated a set of Ag nanoparticles of different sizes with varying surface properties, including polyvinylpyrrolidone (PVP)-coated and poly (ethylene glycol) (PEG)-modified Ag nanoparticles, and found that only the bare (unmodified) nanoparticles were able to prevent virus infection. For comparison, TiO(2) nanoparticles failed to intercept the virus. Proteins and lipids may adsorb to nanoparticles forming a so-called bio-corona; however, Ag nanoparticles pre-incubated with pulmonary surfactant retained their ability to block virus infection in the present model. Furthermore, the secondary structure of the spike protein of SARS-CoV-2 was perturbed by the Ag nanoparticles, but not by the ionic control (AgNO(3)) nor by the TiO(2) nanoparticles. Finally, Ag nanoparticles were shown to be non-cytotoxic towards the human lung epithelial cell line BEAS-2B and this was confirmed by using primary human nasal epithelial cells. These results further support that Ag nanoparticles may find use as anti-viral agents. Frontiers Media S.A. 2022-12-12 /pmc/articles/PMC9790969/ /pubmed/36578508 http://dx.doi.org/10.3389/fbioe.2022.1083232 Text en Copyright © 2022 Gupta, Hamawandi, Sheward, Murrell, Hanke, McInerney, Blosi, Costa, Toprak and Fadeel. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Gupta, Govind
Hamawandi, Bejan
Sheward, Daniel J.
Murrell, Ben
Hanke, Leo
McInerney, Gerald
Blosi, Magda
Costa, Anna L.
Toprak, Muhammet S.
Fadeel, Bengt
Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant
title Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant
title_full Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant
title_fullStr Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant
title_full_unstemmed Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant
title_short Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant
title_sort silver nanoparticles with excellent biocompatibility block pseudotyped sars-cov-2 in the presence of lung surfactant
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790969/
https://www.ncbi.nlm.nih.gov/pubmed/36578508
http://dx.doi.org/10.3389/fbioe.2022.1083232
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