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Nanohole-boosted electron transport between nanomaterials and bacteria as a concept for nano–bio interactions

Biofilms contribute to bacterial infection and drug resistance and are a serious threat to global human health. Antibacterial nanomaterials have attracted considerable attention, but the inhibition of biofilms remains a major challenge. Herein, we propose a nanohole-boosted electron transport (NBET)...

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Autores principales: Shi, Tonglei, Hou, Xuan, Guo, Shuqing, Zhang, Lei, Wei, Changhong, Peng, Ting, Hu, Xiangang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820612/
https://www.ncbi.nlm.nih.gov/pubmed/33479209
http://dx.doi.org/10.1038/s41467-020-20547-9
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author Shi, Tonglei
Hou, Xuan
Guo, Shuqing
Zhang, Lei
Wei, Changhong
Peng, Ting
Hu, Xiangang
author_facet Shi, Tonglei
Hou, Xuan
Guo, Shuqing
Zhang, Lei
Wei, Changhong
Peng, Ting
Hu, Xiangang
author_sort Shi, Tonglei
collection PubMed
description Biofilms contribute to bacterial infection and drug resistance and are a serious threat to global human health. Antibacterial nanomaterials have attracted considerable attention, but the inhibition of biofilms remains a major challenge. Herein, we propose a nanohole-boosted electron transport (NBET) antibiofilm concept. Unlike known antibacterial mechanisms (e.g., reactive oxygen species production and cell membrane damage), nanoholes with atomic vacancies and biofilms serve as electronic donors and receptors, respectively, and thus boost the high electron transport capacity between nanomaterials and biofilms. Electron transport effectively destroys the critical components (proteins, intercellularly adhered polysaccharides and extracellular DNA) of biofilms, and the nanoholes also significantly downregulate the expression of genes related to biofilm formation. The anti-infection capacity is thoroughly verified both in vitro (human cells) and in vivo (rat ocular and mouse intestinal infection models), and the nanohole-enabled nanomaterials are found to be highly biocompatible. Importantly, compared with typical antibiotics, nanomaterials are nonresistant and thereby exhibit high potential for use in various applications. As a proof-of-principle demonstration, these findings hold promise for the use of NBET in treatments for pathogenic bacterial infection and antibiotic drug resistance.
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spelling pubmed-78206122021-01-29 Nanohole-boosted electron transport between nanomaterials and bacteria as a concept for nano–bio interactions Shi, Tonglei Hou, Xuan Guo, Shuqing Zhang, Lei Wei, Changhong Peng, Ting Hu, Xiangang Nat Commun Article Biofilms contribute to bacterial infection and drug resistance and are a serious threat to global human health. Antibacterial nanomaterials have attracted considerable attention, but the inhibition of biofilms remains a major challenge. Herein, we propose a nanohole-boosted electron transport (NBET) antibiofilm concept. Unlike known antibacterial mechanisms (e.g., reactive oxygen species production and cell membrane damage), nanoholes with atomic vacancies and biofilms serve as electronic donors and receptors, respectively, and thus boost the high electron transport capacity between nanomaterials and biofilms. Electron transport effectively destroys the critical components (proteins, intercellularly adhered polysaccharides and extracellular DNA) of biofilms, and the nanoholes also significantly downregulate the expression of genes related to biofilm formation. The anti-infection capacity is thoroughly verified both in vitro (human cells) and in vivo (rat ocular and mouse intestinal infection models), and the nanohole-enabled nanomaterials are found to be highly biocompatible. Importantly, compared with typical antibiotics, nanomaterials are nonresistant and thereby exhibit high potential for use in various applications. As a proof-of-principle demonstration, these findings hold promise for the use of NBET in treatments for pathogenic bacterial infection and antibiotic drug resistance. Nature Publishing Group UK 2021-01-21 /pmc/articles/PMC7820612/ /pubmed/33479209 http://dx.doi.org/10.1038/s41467-020-20547-9 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shi, Tonglei
Hou, Xuan
Guo, Shuqing
Zhang, Lei
Wei, Changhong
Peng, Ting
Hu, Xiangang
Nanohole-boosted electron transport between nanomaterials and bacteria as a concept for nano–bio interactions
title Nanohole-boosted electron transport between nanomaterials and bacteria as a concept for nano–bio interactions
title_full Nanohole-boosted electron transport between nanomaterials and bacteria as a concept for nano–bio interactions
title_fullStr Nanohole-boosted electron transport between nanomaterials and bacteria as a concept for nano–bio interactions
title_full_unstemmed Nanohole-boosted electron transport between nanomaterials and bacteria as a concept for nano–bio interactions
title_short Nanohole-boosted electron transport between nanomaterials and bacteria as a concept for nano–bio interactions
title_sort nanohole-boosted electron transport between nanomaterials and bacteria as a concept for nano–bio interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820612/
https://www.ncbi.nlm.nih.gov/pubmed/33479209
http://dx.doi.org/10.1038/s41467-020-20547-9
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