Serveur d'exploration SRAS

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Viral detection by electron microscopy: past, present and future

Identifieur interne : 003247 ( Main/Exploration ); précédent : 003246; suivant : 003248

Viral detection by electron microscopy: past, present and future

Auteurs : Philippe Roingeard [France]

Source :

RBID : ISTEX:D5B887EF1F5D0FE0A08C328B5F822D8A99B865B0

Abstract

Viruses are very small and most of them can be seen only by TEM (transmission electron microscopy). TEM has therefore made a major contribution to virology, including the discovery of many viruses, the diagnosis of various viral infections and fundamental investigations of virus—host cell interactions. However, TEM has gradually been replaced by more sensitive methods, such as the PCR. In research, new imaging techniques for fluorescence light microscopy have supplanted TEM, making it possible to study live cells and dynamic interactions between viruses and the cellular machinery. Nevertheless, TEM remains essential for certain aspects of virology. It is very useful for the initial identification of unknown viral agents in particular outbreaks, and is recommended by regulatory agencies for investigation of the viral safety of biological products and/or the cells used to produce them. In research, only TEM has a resolution sufficiently high for discrimination between aggregated viral proteins and structured viral particles. Recent examples of different viral assembly models illustrate the value of TEM for improving our understanding of virus—cell interactions.

Url:
DOI: 10.1042/BC20070173


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Viral detection by electron microscopy: past, present and future</title>
<author>
<name sortKey="Roingeard, Philippe" sort="Roingeard, Philippe" uniqKey="Roingeard P" first="Philippe" last="Roingeard">Philippe Roingeard</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:D5B887EF1F5D0FE0A08C328B5F822D8A99B865B0</idno>
<date when="2008" year="2008">2008</date>
<idno type="doi">10.1042/BC20070173</idno>
<idno type="url">https://api.istex.fr/ark:/67375/WNG-7BJW4JQL-F/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000C63</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000C63</idno>
<idno type="wicri:Area/Istex/Curation">000C63</idno>
<idno type="wicri:Area/Istex/Checkpoint">000F21</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">000F21</idno>
<idno type="wicri:doubleKey">0248-4900:2008:Roingeard P:viral:detection:by</idno>
<idno type="wicri:Area/Main/Merge">003349</idno>
<idno type="wicri:Area/Main/Curation">003247</idno>
<idno type="wicri:Area/Main/Exploration">003247</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main">Viral detection by electron microscopy: past, present and future</title>
<author>
<name sortKey="Roingeard, Philippe" sort="Roingeard, Philippe" uniqKey="Roingeard P" first="Philippe" last="Roingeard">Philippe Roingeard</name>
<affiliation wicri:level="3">
<country xml:lang="fr">France</country>
<wicri:regionArea>INSERM ERI 19 and Electron Microscopy Facility, Université François Rabelais and CHRU de Tours, Tours</wicri:regionArea>
<placeName>
<region type="region">Centre-Val de Loire</region>
<region type="old region">Région Centre</region>
<settlement type="city">Tours</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="1">
<country wicri:rule="url">France</country>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j" type="main">Biology of the Cell</title>
<title level="j" type="alt">BIOLOGY OF THE CELL</title>
<idno type="ISSN">0248-4900</idno>
<idno type="eISSN">1768-322X</idno>
<imprint>
<biblScope unit="vol">100</biblScope>
<biblScope unit="issue">8</biblScope>
<biblScope unit="page" from="491">491</biblScope>
<biblScope unit="page" to="501">501</biblScope>
<biblScope unit="page-count">11</biblScope>
<publisher>Blackwell Publishing Ltd</publisher>
<pubPlace>Oxford, UK</pubPlace>
<date type="published" when="2008-08">2008-08</date>
</imprint>
<idno type="ISSN">0248-4900</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0248-4900</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Viruses are very small and most of them can be seen only by TEM (transmission electron microscopy). TEM has therefore made a major contribution to virology, including the discovery of many viruses, the diagnosis of various viral infections and fundamental investigations of virus—host cell interactions. However, TEM has gradually been replaced by more sensitive methods, such as the PCR. In research, new imaging techniques for fluorescence light microscopy have supplanted TEM, making it possible to study live cells and dynamic interactions between viruses and the cellular machinery. Nevertheless, TEM remains essential for certain aspects of virology. It is very useful for the initial identification of unknown viral agents in particular outbreaks, and is recommended by regulatory agencies for investigation of the viral safety of biological products and/or the cells used to produce them. In research, only TEM has a resolution sufficiently high for discrimination between aggregated viral proteins and structured viral particles. Recent examples of different viral assembly models illustrate the value of TEM for improving our understanding of virus—cell interactions.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>France</li>
</country>
<region>
<li>Centre-Val de Loire</li>
<li>Région Centre</li>
</region>
<settlement>
<li>Tours</li>
</settlement>
</list>
<tree>
<country name="France">
<region name="Centre-Val de Loire">
<name sortKey="Roingeard, Philippe" sort="Roingeard, Philippe" uniqKey="Roingeard P" first="Philippe" last="Roingeard">Philippe Roingeard</name>
</region>
<name sortKey="Roingeard, Philippe" sort="Roingeard, Philippe" uniqKey="Roingeard P" first="Philippe" last="Roingeard">Philippe Roingeard</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/SrasV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003247 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 003247 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    SrasV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:D5B887EF1F5D0FE0A08C328B5F822D8A99B865B0
   |texte=   Viral detection by electron microscopy: past, present and future
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Tue Apr 28 14:49:16 2020. Site generation: Sat Mar 27 22:06:49 2021