Serveur d'exploration MERS

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MERS-CoV and H5N1 influenza virus antagonize antigen presentation by altering the epigenetic landscape

Identifieur interne : 000913 ( Main/Exploration ); précédent : 000912; suivant : 000914

MERS-CoV and H5N1 influenza virus antagonize antigen presentation by altering the epigenetic landscape

Auteurs : Vineet D. Menachery ; Alexandra Sch Fer ; Kristin E. Burnum-Johnson ; Hugh D. Mitchell ; Amie J. Eisfeld ; Kevin B. Walters ; Carrie D. Nicora ; Samuel O. Purvine ; Cameron P. Casey ; Matthew E. Monroe ; Karl K. Weitz ; Kelly G. Stratton ; Bobbie-Jo M. Webb-Robertson ; Lisa E. Gralinski ; Thomas O. Metz ; Richard D. Smith ; Katrina M. Waters ; Amy C. Sims ; Yoshihiro Kawaoka [États-Unis, Japon] ; Ralph S. Baric

Source :

RBID : PMC:5798318

Descripteurs français

English descriptors

Abstract

Significance

Both highly pathogenic avian influenza virus and Middle East respiratory syndrome coronavirus (MERS-CoV) infections are characterized by severe disease and high mortality. The continued threat of their emergence from zoonotic populations underscores an important need to understand the dynamics of their infection. By comparing the host responses across other related respiratory virus infections, these studies have identified a common avenue used by MERS-CoV and A/influenza/Vietnam/1203/2004 (H5N1-VN1203) influenza to antagonize antigen presentation through epigenetic modulation. Overall, the use of cross-comparisons provides an additional approach to leverage systems biology data to identify key pathways and strategies used by viruses to subvert host immune responses and may be critical in developing both vaccines and therapeutic treatment.


Url:
DOI: 10.1073/pnas.1706928115
PubMed: 29339515
PubMed Central: 5798318


Affiliations:


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


Le document en format XML

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, Chapel Hill,
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27599;</nlm:aff>
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<addr-line>WI</addr-line>
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, Chapel Hill,
<addr-line>NC</addr-line>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Animals</term>
<term>Antigen Presentation</term>
<term>Antigenic Variation</term>
<term>Cell Line</term>
<term>Chlorocebus aethiops</term>
<term>DNA Methylation</term>
<term>Dogs</term>
<term>Down-Regulation</term>
<term>Epigenesis, Genetic</term>
<term>Histones (chemistry)</term>
<term>Humans</term>
<term>Influenza A Virus, H5N1 Subtype (pathogenicity)</term>
<term>Madin Darby Canine Kidney Cells</term>
<term>Major Histocompatibility Complex</term>
<term>Middle East Respiratory Syndrome Coronavirus (pathogenicity)</term>
<term>Mutation</term>
<term>Open Reading Frames</term>
<term>Proteomics</term>
<term>Vero Cells</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Animaux</term>
<term>Cadres ouverts de lecture</term>
<term>Cellules Vero</term>
<term>Cellules rénales canines Madin-Darby</term>
<term>Chiens</term>
<term>Complexe majeur d'histocompatibilité</term>
<term>Coronavirus du syndrome respiratoire du Moyen-Orient (pathogénicité)</term>
<term>Histone ()</term>
<term>Humains</term>
<term>Lignée cellulaire</term>
<term>Mutation</term>
<term>Méthylation de l'ADN</term>
<term>Protéomique</term>
<term>Présentation d'antigène</term>
<term>Régulation négative</term>
<term>Sous-type H5N1 du virus de la grippe A (pathogénicité)</term>
<term>Variation des antigènes</term>
<term>Épigenèse génétique</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>Histones</term>
</keywords>
<keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en">
<term>Influenza A Virus, H5N1 Subtype</term>
<term>Middle East Respiratory Syndrome Coronavirus</term>
</keywords>
<keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr">
<term>Coronavirus du syndrome respiratoire du Moyen-Orient</term>
<term>Sous-type H5N1 du virus de la grippe A</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Antigen Presentation</term>
<term>Antigenic Variation</term>
<term>Cell Line</term>
<term>Chlorocebus aethiops</term>
<term>DNA Methylation</term>
<term>Dogs</term>
<term>Down-Regulation</term>
<term>Epigenesis, Genetic</term>
<term>Humans</term>
<term>Madin Darby Canine Kidney Cells</term>
<term>Major Histocompatibility Complex</term>
<term>Mutation</term>
<term>Open Reading Frames</term>
<term>Proteomics</term>
<term>Vero Cells</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Cadres ouverts de lecture</term>
<term>Cellules Vero</term>
<term>Cellules rénales canines Madin-Darby</term>
<term>Chiens</term>
<term>Complexe majeur d'histocompatibilité</term>
<term>Histone</term>
<term>Humains</term>
<term>Lignée cellulaire</term>
<term>Mutation</term>
<term>Méthylation de l'ADN</term>
<term>Protéomique</term>
<term>Présentation d'antigène</term>
<term>Régulation négative</term>
<term>Variation des antigènes</term>
<term>Épigenèse génétique</term>
</keywords>
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</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<title>Significance</title>
<p>Both highly pathogenic avian influenza virus and Middle East respiratory syndrome coronavirus (MERS-CoV) infections are characterized by severe disease and high mortality. The continued threat of their emergence from zoonotic populations underscores an important need to understand the dynamics of their infection. By comparing the host responses across other related respiratory virus infections, these studies have identified a common avenue used by MERS-CoV and A/influenza/Vietnam/1203/2004 (H5N1-VN1203) influenza to antagonize antigen presentation through epigenetic modulation. Overall, the use of cross-comparisons provides an additional approach to leverage systems biology data to identify key pathways and strategies used by viruses to subvert host immune responses and may be critical in developing both vaccines and therapeutic treatment.</p>
</div>
</front>
<back>
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<list>
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<li>Japon</li>
<li>États-Unis</li>
</country>
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<li>Région de Kantō</li>
<li>Wisconsin</li>
</region>
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<li>Madison (Wisconsin)</li>
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</settlement>
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<name sortKey="Metz, Thomas O" sort="Metz, Thomas O" uniqKey="Metz T" first="Thomas O." last="Metz">Thomas O. Metz</name>
<name sortKey="Mitchell, Hugh D" sort="Mitchell, Hugh D" uniqKey="Mitchell H" first="Hugh D." last="Mitchell">Hugh D. Mitchell</name>
<name sortKey="Monroe, Matthew E" sort="Monroe, Matthew E" uniqKey="Monroe M" first="Matthew E." last="Monroe">Matthew E. Monroe</name>
<name sortKey="Nicora, Carrie D" sort="Nicora, Carrie D" uniqKey="Nicora C" first="Carrie D." last="Nicora">Carrie D. Nicora</name>
<name sortKey="Purvine, Samuel O" sort="Purvine, Samuel O" uniqKey="Purvine S" first="Samuel O." last="Purvine">Samuel O. Purvine</name>
<name sortKey="Sch Fer, Alexandra" sort="Sch Fer, Alexandra" uniqKey="Sch Fer A" first="Alexandra" last="Sch Fer">Alexandra Sch Fer</name>
<name sortKey="Sims, Amy C" sort="Sims, Amy C" uniqKey="Sims A" first="Amy C." last="Sims">Amy C. Sims</name>
<name sortKey="Smith, Richard D" sort="Smith, Richard D" uniqKey="Smith R" first="Richard D." last="Smith">Richard D. Smith</name>
<name sortKey="Stratton, Kelly G" sort="Stratton, Kelly G" uniqKey="Stratton K" first="Kelly G." last="Stratton">Kelly G. Stratton</name>
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<name sortKey="Waters, Katrina M" sort="Waters, Katrina M" uniqKey="Waters K" first="Katrina M." last="Waters">Katrina M. Waters</name>
<name sortKey="Webb Robertson, Bobbie Jo M" sort="Webb Robertson, Bobbie Jo M" uniqKey="Webb Robertson B" first="Bobbie-Jo M." last="Webb-Robertson">Bobbie-Jo M. Webb-Robertson</name>
<name sortKey="Weitz, Karl K" sort="Weitz, Karl K" uniqKey="Weitz K" first="Karl K." last="Weitz">Karl K. Weitz</name>
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<region name="Wisconsin">
<name sortKey="Kawaoka, Yoshihiro" sort="Kawaoka, Yoshihiro" uniqKey="Kawaoka Y" first="Yoshihiro" last="Kawaoka">Yoshihiro Kawaoka</name>
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<region name="Région de Kantō">
<name sortKey="Kawaoka, Yoshihiro" sort="Kawaoka, Yoshihiro" uniqKey="Kawaoka Y" first="Yoshihiro" last="Kawaoka">Yoshihiro Kawaoka</name>
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<name sortKey="Kawaoka, Yoshihiro" sort="Kawaoka, Yoshihiro" uniqKey="Kawaoka Y" first="Yoshihiro" last="Kawaoka">Yoshihiro Kawaoka</name>
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