Cargando…
Concentration of SARS-CoV-2-Infected Cell Culture Supernatants for Detection of Virus-like Particles by Scanning Electron Microscopy
There is currently a need for new rapid viral diagnostic electron microscopy methods. Although the gold standard remains the transmission electron microscopy (TEM) negative staining method for electron microscopic examination of samples containing a virus, difficulties can arise when the virus parti...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698492/ https://www.ncbi.nlm.nih.gov/pubmed/36366486 http://dx.doi.org/10.3390/v14112388 |
_version_ | 1784838832615587840 |
---|---|
author | Le Bideau, Marion Robresco, Lea Baudoin, Jean-Pierre La Scola, Bernard |
author_facet | Le Bideau, Marion Robresco, Lea Baudoin, Jean-Pierre La Scola, Bernard |
author_sort | Le Bideau, Marion |
collection | PubMed |
description | There is currently a need for new rapid viral diagnostic electron microscopy methods. Although the gold standard remains the transmission electron microscopy (TEM) negative staining method for electron microscopic examination of samples containing a virus, difficulties can arise when the virus particle content of the sample that has to be examined is poor. Such samples include supernatants of virus-infected cells that can be difficult to examine, as sometimes only a few virus particles are released in the culture medium upon infection. In addition to TEM, scanning electron microscopy (SEM) can also be used for visualizing virus particles. One advantage of SEM over TEM is its ability to rapidly screen several large specimens, such as microscopy slides. In this study, we investigated this possibility and tested different coating molecules as well as the effect of centrifugation for analyzing SARS-CoV-2-virus-infected cell culture supernatants deposited on microscopy glass slides by SEM. We found that centrifugation of 25XConcanavalinA-coated microscopy glass slides in shell vials provided an improved method for concentrating SARS-CoV-2-virus-infected cell supernatants for virus-like particle detection by SEM. |
format | Online Article Text |
id | pubmed-9698492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96984922022-11-26 Concentration of SARS-CoV-2-Infected Cell Culture Supernatants for Detection of Virus-like Particles by Scanning Electron Microscopy Le Bideau, Marion Robresco, Lea Baudoin, Jean-Pierre La Scola, Bernard Viruses Article There is currently a need for new rapid viral diagnostic electron microscopy methods. Although the gold standard remains the transmission electron microscopy (TEM) negative staining method for electron microscopic examination of samples containing a virus, difficulties can arise when the virus particle content of the sample that has to be examined is poor. Such samples include supernatants of virus-infected cells that can be difficult to examine, as sometimes only a few virus particles are released in the culture medium upon infection. In addition to TEM, scanning electron microscopy (SEM) can also be used for visualizing virus particles. One advantage of SEM over TEM is its ability to rapidly screen several large specimens, such as microscopy slides. In this study, we investigated this possibility and tested different coating molecules as well as the effect of centrifugation for analyzing SARS-CoV-2-virus-infected cell culture supernatants deposited on microscopy glass slides by SEM. We found that centrifugation of 25XConcanavalinA-coated microscopy glass slides in shell vials provided an improved method for concentrating SARS-CoV-2-virus-infected cell supernatants for virus-like particle detection by SEM. MDPI 2022-10-28 /pmc/articles/PMC9698492/ /pubmed/36366486 http://dx.doi.org/10.3390/v14112388 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Le Bideau, Marion Robresco, Lea Baudoin, Jean-Pierre La Scola, Bernard Concentration of SARS-CoV-2-Infected Cell Culture Supernatants for Detection of Virus-like Particles by Scanning Electron Microscopy |
title | Concentration of SARS-CoV-2-Infected Cell Culture Supernatants for Detection of Virus-like Particles by Scanning Electron Microscopy |
title_full | Concentration of SARS-CoV-2-Infected Cell Culture Supernatants for Detection of Virus-like Particles by Scanning Electron Microscopy |
title_fullStr | Concentration of SARS-CoV-2-Infected Cell Culture Supernatants for Detection of Virus-like Particles by Scanning Electron Microscopy |
title_full_unstemmed | Concentration of SARS-CoV-2-Infected Cell Culture Supernatants for Detection of Virus-like Particles by Scanning Electron Microscopy |
title_short | Concentration of SARS-CoV-2-Infected Cell Culture Supernatants for Detection of Virus-like Particles by Scanning Electron Microscopy |
title_sort | concentration of sars-cov-2-infected cell culture supernatants for detection of virus-like particles by scanning electron microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698492/ https://www.ncbi.nlm.nih.gov/pubmed/36366486 http://dx.doi.org/10.3390/v14112388 |
work_keys_str_mv | AT lebideaumarion concentrationofsarscov2infectedcellculturesupernatantsfordetectionofviruslikeparticlesbyscanningelectronmicroscopy AT robrescolea concentrationofsarscov2infectedcellculturesupernatantsfordetectionofviruslikeparticlesbyscanningelectronmicroscopy AT baudoinjeanpierre concentrationofsarscov2infectedcellculturesupernatantsfordetectionofviruslikeparticlesbyscanningelectronmicroscopy AT lascolabernard concentrationofsarscov2infectedcellculturesupernatantsfordetectionofviruslikeparticlesbyscanningelectronmicroscopy |