The Strengths of Scanning Electron Microscopy in Deciphering SARS-CoV-2 Infectious Cycle

Electron microscopy is a powerful tool in the field of microbiology. It has played a key role in the rapid diagnosis of viruses in patient samples and has contributed significantly to the clarification of virus structure and function, helping to guide the public health response to emerging viral inf...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in microbiology Vol. 11; p. 2014
Main Authors Brahim Belhaouari, Djamal, Fontanini, Anthony, Baudoin, Jean-Pierre, Haddad, Gabriel, Le Bideau, Marion, Bou Khalil, Jacques Yaacoub, Raoult, Didier, La Scola, Bernard
Format Journal Article
LanguageEnglish
Published Frontiers Media 19.08.2020
Frontiers Media S.A
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Electron microscopy is a powerful tool in the field of microbiology. It has played a key role in the rapid diagnosis of viruses in patient samples and has contributed significantly to the clarification of virus structure and function, helping to guide the public health response to emerging viral infections. In the present study, we used scanning electron microscopy (SEM) to study the infectious cycle of SARS-CoV-2 in Vero E6 cells and we controlled some key findings by classical transmission electronic microscopy (TEM). The replication cycle of the virus was followed from 1 to 36 h post-infection. Our results revealed that SARS-CoV-2 infected the cells through membrane fusion. Particles are formed in the peri-nuclear region from a budding of the endoplasmic reticulum-Golgi apparatus complex into morphogenesis matrix vesicae. New SARS-CoV-2 particles were expelled from the cells, through cell lysis or by fusion of virus containing vacuoles with the cell plasma membrane. Overall, this cycle is highly comparable to that of SARS-CoV. By providing a detailed and complete SARS-CoV-2 infectious cycle, SEM proves to be a very rapid and efficient tool compared to classical TEM.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMCID: PMC7466455
Reviewed by: Maria C. Silva, Federal University of ABC, Brazil; Joel D. Baines, Louisiana State University, United States
This article was submitted to Virology, a section of the journal Frontiers in Microbiology
Edited by: Fatah Kashanchi, George Mason University, United States
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2020.02014