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The replication of a mouse adapted SARS-CoV in a mouse cell line stably expressing the murine SARS-CoV receptor mACE2 efficiently induces the expression of proinflammatory cytokines

Identifieur interne : 002722 ( Ncbi/Merge ); précédent : 002721; suivant : 002723

The replication of a mouse adapted SARS-CoV in a mouse cell line stably expressing the murine SARS-CoV receptor mACE2 efficiently induces the expression of proinflammatory cytokines

Auteurs : Jose A. Regla-Nava [Espagne] ; Jose M. Jimenez-Guarde O [Espagne] ; Jose L. Nieto-Torres [Espagne] ; Thomas M. Gallagher [États-Unis] ; Luis Enjuanes [Espagne] ; Marta L. Dediego [Espagne]

Source :

RBID : PMC:3805046

Descripteurs français

English descriptors

Abstract

Highlights

Delayed brain tumor (DBT) mouse cell lines stably expressing the murine angiotensin converting enzyme 2 (mACE2) have been generated.

The cell lines are highly susceptible to mouse-adapted SARS-CoV infection.

SARS-CoV-MA15 efficiently induced the expression of proinflammatory cytokines and IFN-β in DBT-mACE2 cells.

DBT-mACE2 cells provide a good experimental system that is species-homologous to the in vivo systems for evaluating SARS-CoV-host interaction studies.


Url:
DOI: 10.1016/j.jviromet.2013.07.039
PubMed: 23911968
PubMed Central: 3805046

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PMC:3805046

Le document en format XML

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<p id="par0005">Delayed brain tumor (DBT) mouse cell lines stably expressing the murine angiotensin converting enzyme 2 (mACE2) have been generated.</p>
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<p id="par0010">The cell lines are highly susceptible to mouse-adapted SARS-CoV infection.</p>
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<title level="j">Journal of Virological Methods</title>
<idno type="ISSN">0166-0934</idno>
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<title>Highlights</title>
<p>
<list list-type="simple" id="lis0005">
<list-item id="lsti0005">
<label></label>
<p id="par0005">Delayed brain tumor (DBT) mouse cell lines stably expressing the murine angiotensin converting enzyme 2 (mACE2) have been generated.</p>
</list-item>
<list-item id="lsti0010">
<label></label>
<p id="par0010">The cell lines are highly susceptible to mouse-adapted SARS-CoV infection.</p>
</list-item>
<list-item id="lsti0015">
<label></label>
<p id="par0015">SARS-CoV-MA15 efficiently induced the expression of proinflammatory cytokines and IFN-β in DBT-mACE2 cells.</p>
</list-item>
<list-item id="lsti0020">
<label></label>
<p id="par0020">DBT-mACE2 cells provide a good experimental system that is species-homologous to the in vivo systems for evaluating SARS-CoV-host interaction studies.</p>
</list-item>
</list>
</p>
</div>
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<title xml:lang="en">The replication of a mouse adapted SARS-CoV in a mouse cell line stably expressing the murine SARS-CoV receptor mACE2 efficiently induces the expression of proinflammatory cytokines.</title>
<author>
<name sortKey="Regla Nava, Jose A" sort="Regla Nava, Jose A" uniqKey="Regla Nava J" first="Jose A" last="Regla-Nava">Jose A. Regla-Nava</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Molecular and Cell Biology, Centro Nacional de Biotecnología (CNB-CSIC), Darwin 3, Campus Universidad Autónoma de Madrid, 28049 Madrid, Spain.</nlm:affiliation>
<country xml:lang="fr">Espagne</country>
<wicri:regionArea>Department of Molecular and Cell Biology, Centro Nacional de Biotecnología (CNB-CSIC), Darwin 3, Campus Universidad Autónoma de Madrid, 28049 Madrid</wicri:regionArea>
<placeName>
<region nuts="2" type="communauté">Communauté de Madrid</region>
<settlement type="city">Madrid</settlement>
</placeName>
<orgName type="university">Université autonome de Madrid</orgName>
</affiliation>
</author>
<author>
<name sortKey="Jimenez Guarde O, Jose M" sort="Jimenez Guarde O, Jose M" uniqKey="Jimenez Guarde O J" first="Jose M" last="Jimenez-Guarde O">Jose M. Jimenez-Guarde O</name>
</author>
<author>
<name sortKey="Nieto Torres, Jose L" sort="Nieto Torres, Jose L" uniqKey="Nieto Torres J" first="Jose L" last="Nieto-Torres">Jose L. Nieto-Torres</name>
</author>
<author>
<name sortKey="Gallagher, Thomas M" sort="Gallagher, Thomas M" uniqKey="Gallagher T" first="Thomas M" last="Gallagher">Thomas M. Gallagher</name>
</author>
<author>
<name sortKey="Enjuanes, Luis" sort="Enjuanes, Luis" uniqKey="Enjuanes L" first="Luis" last="Enjuanes">Luis Enjuanes</name>
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<author>
<name sortKey="Dediego, Marta L" sort="Dediego, Marta L" uniqKey="Dediego M" first="Marta L" last="Dediego">Marta L. Dediego</name>
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<idno type="RBID">pubmed:23911968</idno>
<idno type="pmid">23911968</idno>
<idno type="doi">10.1016/j.jviromet.2013.07.039</idno>
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<title xml:lang="en">The replication of a mouse adapted SARS-CoV in a mouse cell line stably expressing the murine SARS-CoV receptor mACE2 efficiently induces the expression of proinflammatory cytokines.</title>
<author>
<name sortKey="Regla Nava, Jose A" sort="Regla Nava, Jose A" uniqKey="Regla Nava J" first="Jose A" last="Regla-Nava">Jose A. Regla-Nava</name>
<affiliation wicri:level="4">
<nlm:affiliation>Department of Molecular and Cell Biology, Centro Nacional de Biotecnología (CNB-CSIC), Darwin 3, Campus Universidad Autónoma de Madrid, 28049 Madrid, Spain.</nlm:affiliation>
<country xml:lang="fr">Espagne</country>
<wicri:regionArea>Department of Molecular and Cell Biology, Centro Nacional de Biotecnología (CNB-CSIC), Darwin 3, Campus Universidad Autónoma de Madrid, 28049 Madrid</wicri:regionArea>
<placeName>
<region nuts="2" type="communauté">Communauté de Madrid</region>
<settlement type="city">Madrid</settlement>
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<author>
<name sortKey="Jimenez Guarde O, Jose M" sort="Jimenez Guarde O, Jose M" uniqKey="Jimenez Guarde O J" first="Jose M" last="Jimenez-Guarde O">Jose M. Jimenez-Guarde O</name>
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<author>
<name sortKey="Nieto Torres, Jose L" sort="Nieto Torres, Jose L" uniqKey="Nieto Torres J" first="Jose L" last="Nieto-Torres">Jose L. Nieto-Torres</name>
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<author>
<name sortKey="Gallagher, Thomas M" sort="Gallagher, Thomas M" uniqKey="Gallagher T" first="Thomas M" last="Gallagher">Thomas M. Gallagher</name>
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<author>
<name sortKey="Enjuanes, Luis" sort="Enjuanes, Luis" uniqKey="Enjuanes L" first="Luis" last="Enjuanes">Luis Enjuanes</name>
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<author>
<name sortKey="Dediego, Marta L" sort="Dediego, Marta L" uniqKey="Dediego M" first="Marta L" last="Dediego">Marta L. Dediego</name>
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<title level="j">Journal of virological methods</title>
<idno type="eISSN">1879-0984</idno>
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<term>Adaptation, Biological</term>
<term>Animals</term>
<term>Cell Line</term>
<term>Cytokines (biosynthesis)</term>
<term>Gene Expression</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Peptidyl-Dipeptidase A (genetics)</term>
<term>Peptidyl-Dipeptidase A (metabolism)</term>
<term>SARS Virus (growth & development)</term>
<term>SARS Virus (immunology)</term>
<term>Viral Load</term>
<term>Viral Plaque Assay</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adaptation biologique</term>
<term>Animaux</term>
<term>Charge virale</term>
<term>Cytokines (biosynthèse)</term>
<term>Expression des gènes</term>
<term>Lignée cellulaire</term>
<term>Méthode des plages virales</term>
<term>Peptidyl-Dipeptidase A (génétique)</term>
<term>Peptidyl-Dipeptidase A (métabolisme)</term>
<term>Souris</term>
<term>Souris de lignée BALB C</term>
<term>Virus du SRAS (croissance et développement)</term>
<term>Virus du SRAS (immunologie)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en">
<term>Cytokines</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Peptidyl-Dipeptidase A</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Peptidyl-Dipeptidase A</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr">
<term>Cytokines</term>
</keywords>
<keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr">
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" qualifier="growth & development" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Peptidyl-Dipeptidase A</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr">
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Peptidyl-Dipeptidase A</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adaptation, Biological</term>
<term>Animals</term>
<term>Cell Line</term>
<term>Gene Expression</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Viral Load</term>
<term>Viral Plaque Assay</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adaptation biologique</term>
<term>Animaux</term>
<term>Charge virale</term>
<term>Expression des gènes</term>
<term>Lignée cellulaire</term>
<term>Méthode des plages virales</term>
<term>Souris</term>
<term>Souris de lignée BALB C</term>
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<front>
<div type="abstract" xml:lang="en">Infection of conventional mice with a mouse adapted (MA15) severe acute respiratory syndrome (SARS) coronavirus (CoV) reproduces many aspects of human SARS such as pathological changes in lung, viremia, neutrophilia, and lethality. However, established mouse cell lines highly susceptible to mouse-adapted SARS-CoV infection are not available. In this work, efficiently transfectable mouse cell lines stably expressing the murine SARS-CoV receptor angiotensin converting enzyme 2 (ACE2) have been generated. These cells yielded high SARS-CoV-MA15 titers and also served as excellent tools for plaque assays. In addition, in these cell lines, SARS-CoV-MA15 induced the expression of proinflammatory cytokines and IFN-β, mimicking what has been observed in experimental animal models infected with SARS-CoV and SARS patients. These cell lines are valuable tools to perform in vitro studies in a mouse cell system that reflects the species used for in vivo studies of SARS-CoV-MA15 pathogenesis. </div>
</front>
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