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Sulfated endospermic nanocellulose crystals prevent the transmission of SARS-CoV-2 and HIV-1

Biomaterials with antimicrobial activity are gaining attention due to their biodegradability and efficacy in interacting with a wide range of microorganisms. A new cellulose nano-biomaterial, endospermic nanocellulose crystals (ENC) obtained from parenchymal tissue of ivory nut endosperm, has a natu...

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Autores principales: Carvajal-Barriga, Enrique Javier, Fitzgerald, Wendy, Dimitriadis, Emilios K., Margolis, Leonid, Fields, R. Douglas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141831/
https://www.ncbi.nlm.nih.gov/pubmed/37117231
http://dx.doi.org/10.1038/s41598-023-33686-y
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author Carvajal-Barriga, Enrique Javier
Fitzgerald, Wendy
Dimitriadis, Emilios K.
Margolis, Leonid
Fields, R. Douglas
author_facet Carvajal-Barriga, Enrique Javier
Fitzgerald, Wendy
Dimitriadis, Emilios K.
Margolis, Leonid
Fields, R. Douglas
author_sort Carvajal-Barriga, Enrique Javier
collection PubMed
description Biomaterials with antimicrobial activity are gaining attention due to their biodegradability and efficacy in interacting with a wide range of microorganisms. A new cellulose nano-biomaterial, endospermic nanocellulose crystals (ENC) obtained from parenchymal tissue of ivory nut endosperm, has a natural capacity as a universal binder. This feature is enhanced when it is chemically functionalized, and can be exploited in the fight against microbes. We tested the ability of sulfated ENC in aqueous suspension to encapsulate viruses through a crosslinking reaction mediated by cations. 0.25% w/v ENC suspensions efficiently encapsulated spike (S) protein, preventing its interaction with ACE2 receptor. ENC was further able to encapsulate SARS-CoV-2 pseudoviruses and prevent infection of 293T-hsACE2 cells. ENC also suppressed infection of MT-4 cells with HIV-1(LAI.04). This antiviral activity of sulfated ENC is due to the irreversible interaction of ENC with viral particles mediated by crosslinking, as antiviral activity was less effective in the absence of cations. Additionally, ENC was used as a matrix to immobilize recombinant ACE2 receptors and anti-S IgG, creating molecular lures that efficiently inhibited SARS-CoV-2 infections in vitro. These results show that sulfated ENC from ivory nuts can be used as an efficient antiviral material.
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spelling pubmed-101418312023-04-30 Sulfated endospermic nanocellulose crystals prevent the transmission of SARS-CoV-2 and HIV-1 Carvajal-Barriga, Enrique Javier Fitzgerald, Wendy Dimitriadis, Emilios K. Margolis, Leonid Fields, R. Douglas Sci Rep Article Biomaterials with antimicrobial activity are gaining attention due to their biodegradability and efficacy in interacting with a wide range of microorganisms. A new cellulose nano-biomaterial, endospermic nanocellulose crystals (ENC) obtained from parenchymal tissue of ivory nut endosperm, has a natural capacity as a universal binder. This feature is enhanced when it is chemically functionalized, and can be exploited in the fight against microbes. We tested the ability of sulfated ENC in aqueous suspension to encapsulate viruses through a crosslinking reaction mediated by cations. 0.25% w/v ENC suspensions efficiently encapsulated spike (S) protein, preventing its interaction with ACE2 receptor. ENC was further able to encapsulate SARS-CoV-2 pseudoviruses and prevent infection of 293T-hsACE2 cells. ENC also suppressed infection of MT-4 cells with HIV-1(LAI.04). This antiviral activity of sulfated ENC is due to the irreversible interaction of ENC with viral particles mediated by crosslinking, as antiviral activity was less effective in the absence of cations. Additionally, ENC was used as a matrix to immobilize recombinant ACE2 receptors and anti-S IgG, creating molecular lures that efficiently inhibited SARS-CoV-2 infections in vitro. These results show that sulfated ENC from ivory nuts can be used as an efficient antiviral material. Nature Publishing Group UK 2023-04-28 /pmc/articles/PMC10141831/ /pubmed/37117231 http://dx.doi.org/10.1038/s41598-023-33686-y Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 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
Carvajal-Barriga, Enrique Javier
Fitzgerald, Wendy
Dimitriadis, Emilios K.
Margolis, Leonid
Fields, R. Douglas
Sulfated endospermic nanocellulose crystals prevent the transmission of SARS-CoV-2 and HIV-1
title Sulfated endospermic nanocellulose crystals prevent the transmission of SARS-CoV-2 and HIV-1
title_full Sulfated endospermic nanocellulose crystals prevent the transmission of SARS-CoV-2 and HIV-1
title_fullStr Sulfated endospermic nanocellulose crystals prevent the transmission of SARS-CoV-2 and HIV-1
title_full_unstemmed Sulfated endospermic nanocellulose crystals prevent the transmission of SARS-CoV-2 and HIV-1
title_short Sulfated endospermic nanocellulose crystals prevent the transmission of SARS-CoV-2 and HIV-1
title_sort sulfated endospermic nanocellulose crystals prevent the transmission of sars-cov-2 and hiv-1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141831/
https://www.ncbi.nlm.nih.gov/pubmed/37117231
http://dx.doi.org/10.1038/s41598-023-33686-y
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