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Correlative ex situ and Liquid-Cell TEM Observation of Bacterial Cell Membrane Damage Induced by Rough Surface Topology

BACKGROUND: Nanoscale surface roughness has been suggested to have antibacterial and antifouling properties. Several existing models have attempted to explain the antibacterial mechanism of nanoscale rough surfaces without direct observation. Here, conventional and liquid-cell TEM are implemented to...

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Autores principales: Banner, David J, Firlar, Emre, Jakubonis, Justas, Baggia, Yusuf, Osborn, Jodi K, Shahbazian-Yassar, Reza, Megaridis, Constantine M, Shokuhfar, Tolou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093104/
https://www.ncbi.nlm.nih.gov/pubmed/32256069
http://dx.doi.org/10.2147/IJN.S232230
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author Banner, David J
Firlar, Emre
Jakubonis, Justas
Baggia, Yusuf
Osborn, Jodi K
Shahbazian-Yassar, Reza
Megaridis, Constantine M
Shokuhfar, Tolou
author_facet Banner, David J
Firlar, Emre
Jakubonis, Justas
Baggia, Yusuf
Osborn, Jodi K
Shahbazian-Yassar, Reza
Megaridis, Constantine M
Shokuhfar, Tolou
author_sort Banner, David J
collection PubMed
description BACKGROUND: Nanoscale surface roughness has been suggested to have antibacterial and antifouling properties. Several existing models have attempted to explain the antibacterial mechanism of nanoscale rough surfaces without direct observation. Here, conventional and liquid-cell TEM are implemented to observe nanoscale bacteria/surface roughness interaction. The visualization of such interactions enables the inference of possible antibacterial mechanisms. METHODS AND RESULTS: Nanotextures are synthesized on biocompatible polymer microparticles (MPs) via plasma etching. Both conventional and liquid-phase transmission electron microscopy observations suggest that these MPs may cause cell lysis via bacterial binding to a single protrusion of the nanotexture. The bacterium/protrusion interaction locally compromises the cell wall, thus causing bacterial death. This study suggests that local mechanical damage and leakage of the cytosol kill the bacteria first, with subsequent degradation of the cell envelope. CONCLUSION: Nanoscale surface roughness may act via a penetrative bactericidal mechanism. This insight suggests that future research may focus on optimizing bacterial binding to individual nanoscale projections in addition to stretching bacteria between nanopillars. Further, antibacterial nanotextures may find use in novel applications employing particles in addition to nanotextures on fibers or films.
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spelling pubmed-70931042020-04-01 Correlative ex situ and Liquid-Cell TEM Observation of Bacterial Cell Membrane Damage Induced by Rough Surface Topology Banner, David J Firlar, Emre Jakubonis, Justas Baggia, Yusuf Osborn, Jodi K Shahbazian-Yassar, Reza Megaridis, Constantine M Shokuhfar, Tolou Int J Nanomedicine Original Research BACKGROUND: Nanoscale surface roughness has been suggested to have antibacterial and antifouling properties. Several existing models have attempted to explain the antibacterial mechanism of nanoscale rough surfaces without direct observation. Here, conventional and liquid-cell TEM are implemented to observe nanoscale bacteria/surface roughness interaction. The visualization of such interactions enables the inference of possible antibacterial mechanisms. METHODS AND RESULTS: Nanotextures are synthesized on biocompatible polymer microparticles (MPs) via plasma etching. Both conventional and liquid-phase transmission electron microscopy observations suggest that these MPs may cause cell lysis via bacterial binding to a single protrusion of the nanotexture. The bacterium/protrusion interaction locally compromises the cell wall, thus causing bacterial death. This study suggests that local mechanical damage and leakage of the cytosol kill the bacteria first, with subsequent degradation of the cell envelope. CONCLUSION: Nanoscale surface roughness may act via a penetrative bactericidal mechanism. This insight suggests that future research may focus on optimizing bacterial binding to individual nanoscale projections in addition to stretching bacteria between nanopillars. Further, antibacterial nanotextures may find use in novel applications employing particles in addition to nanotextures on fibers or films. Dove 2020-03-20 /pmc/articles/PMC7093104/ /pubmed/32256069 http://dx.doi.org/10.2147/IJN.S232230 Text en © 2020 Banner et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Banner, David J
Firlar, Emre
Jakubonis, Justas
Baggia, Yusuf
Osborn, Jodi K
Shahbazian-Yassar, Reza
Megaridis, Constantine M
Shokuhfar, Tolou
Correlative ex situ and Liquid-Cell TEM Observation of Bacterial Cell Membrane Damage Induced by Rough Surface Topology
title Correlative ex situ and Liquid-Cell TEM Observation of Bacterial Cell Membrane Damage Induced by Rough Surface Topology
title_full Correlative ex situ and Liquid-Cell TEM Observation of Bacterial Cell Membrane Damage Induced by Rough Surface Topology
title_fullStr Correlative ex situ and Liquid-Cell TEM Observation of Bacterial Cell Membrane Damage Induced by Rough Surface Topology
title_full_unstemmed Correlative ex situ and Liquid-Cell TEM Observation of Bacterial Cell Membrane Damage Induced by Rough Surface Topology
title_short Correlative ex situ and Liquid-Cell TEM Observation of Bacterial Cell Membrane Damage Induced by Rough Surface Topology
title_sort correlative ex situ and liquid-cell tem observation of bacterial cell membrane damage induced by rough surface topology
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093104/
https://www.ncbi.nlm.nih.gov/pubmed/32256069
http://dx.doi.org/10.2147/IJN.S232230
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