3D Electron Microscopy (EM) and Correlative Light Electron Microscopy (CLEM) methods to study virus-host interactions

Viruses use different strategies to interact with their host and perform a successful viral infection that results in the formation of new infectious viral particles and their propagation to new hosts. Understanding how viruses interact with their hosts requires the use of high-resolution techniques...

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1. Verfasser: Romero-Brey, Inés (VerfasserIn)
Dokumenttyp: Kapitel/Artikel
Sprache:Englisch
Veröffentlicht: 28 August 2018
In: Influenza virus
Year: 2018, Pages: 213-236
DOI:10.1007/978-1-4939-8678-1_11
Online-Zugang:Verlag, Volltext: https://doi.org/10.1007/978-1-4939-8678-1_11
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Verfasserangaben:Inés Romero-Brey

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520 |a Viruses use different strategies to interact with their host and perform a successful viral infection that results in the formation of new infectious viral particles and their propagation to new hosts. Understanding how viruses interact with their hosts requires the use of high-resolution techniques for the direct visualization of these interactions. Here electron microscopy (EM) methods are described that allow the 3D ultrastructural analysis of virus-infected cells. These methods can be implemented with light microscopy (LM) to certainly allocate virus-infected cells or cells displaying a specific/interesting phenotype caused by the interaction of viral proteins with the cellular machinery. Some sample preparation procedures where LM is integrated, known as correlative light electron microscopy (CLEM), are also explained in this chapter. All of these methods are applicable to any kind of cultured cells, including influenza virus-infected cells. 
650 4 |a Chemical fixation 
650 4 |a Correlative light and electron microscopy 
650 4 |a Cryo-immobilization 
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650 4 |a Focused ion beam-scanning electron microscopy 
650 4 |a Freeze-substitution 
650 4 |a High-pressure freezing 
650 4 |a Ultrastructure 
650 4 |a Virus-induced cellular rearrangements 
650 4 |a Virus-infected cells 
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