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Conservation of a unique mechanism of immune evasion across the Lyssavirus genus.

Identifieur interne : 000121 ( Hal/Curation ); précédent : 000120; suivant : 000122

Conservation of a unique mechanism of immune evasion across the Lyssavirus genus.

Auteurs : L. Wiltzer [Australie] ; Florence Larrous [France] ; S. Oksayan [Australie] ; N. Ito [Japon] ; G A Marsh ; L F Wang [Canada] ; D. Blondel [France] ; Hervé Bourhy [France] ; D A Jans [Australie] ; G W Moseley [Australie]

Source :

RBID : Hal:pasteur-01481638

English descriptors

Abstract

The evasion of host innate immunity by Rabies virus, the prototype of the genus Lyssavirus, depends on a unique mechanism of selective targeting of interferon-activated STAT proteins by the viral phosphoprotein (P-protein). However, the immune evasion strategies of other lyssaviruses, including several lethal human pathogens, are unresolved. Here, we show that this mechanism is conserved between the most distantly related members of the genus, providing important insights into the pathogenesis and potential therapeutic targeting of lyssaviruses.


Url:
DOI: 10.1128/JVI.01249-12

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Hal:pasteur-01481638

Le document en format XML

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<p>The evasion of host innate immunity by Rabies virus, the prototype of the genus Lyssavirus, depends on a unique mechanism of selective targeting of interferon-activated STAT proteins by the viral phosphoprotein (P-protein). However, the immune evasion strategies of other lyssaviruses, including several lethal human pathogens, are unresolved. Here, we show that this mechanism is conserved between the most distantly related members of the genus, providing important insights into the pathogenesis and potential therapeutic targeting of lyssaviruses.</p>
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<funder>This research was supported by the National Health and Medical Research Council Australia project grant 1003244 to G.W.M., Senior Principal Research Fellowship 1002486 to D.A.J., Australian Research Council discovery project grant DP110101749 to G.W.M., D.A.J., and L.F.W., and European Union Seventh Framework Programme (FP7/2007-2013) PREDEMICS grant 278433 to F.L. and H.B. </funder>
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<idno type="stamp" n="UNIV-PARIS7" corresp="UNIV-PARIS">Université Denis Diderot - Paris VII</idno>
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<title xml:lang="en">Conservation of a unique mechanism of immune evasion across the Lyssavirus genus.</title>
<author role="aut">
<persName>
<forename type="first">L.</forename>
<surname>Wiltzer</surname>
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<author role="aut">
<persName>
<forename type="first">Florence</forename>
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<persName>
<forename type="first">G A</forename>
<surname>Marsh</surname>
</persName>
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</author>
<author role="aut">
<persName>
<forename type="first">L F</forename>
<surname>Wang</surname>
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<author role="aut">
<persName>
<forename type="first">D</forename>
<surname>Blondel</surname>
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</author>
<author role="aut">
<persName>
<forename type="first">Hervé</forename>
<surname>Bourhy</surname>
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<email type="md5">5c042ae4dc70a704d897924d6bd2e227</email>
<email type="domain">pasteur.fr</email>
<idno type="idhal" notation="string">herve-bourhy</idno>
<idno type="idhal" notation="numeric">11293</idno>
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<idno type="ORCID">https://orcid.org/0000-0002-2608-5589</idno>
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<forename type="first">D A</forename>
<surname>Jans</surname>
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<idno type="halauthorid">1504699</idno>
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</author>
<author role="aut">
<persName>
<forename type="first">G W</forename>
<surname>Moseley</surname>
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<idno type="halauthorid">1504700</idno>
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<idno type="halJournalId" status="VALID">6614</idno>
<idno type="issn">0022-538X</idno>
<idno type="eissn">1098-5514</idno>
<title level="j">Journal of Virology</title>
<imprint>
<publisher>American Society for Microbiology</publisher>
<biblScope unit="volume">86</biblScope>
<biblScope unit="issue">18</biblScope>
<biblScope unit="pp">10194-9</biblScope>
<date type="datePub">2012-09</date>
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<idno type="doi">10.1128/JVI.01249-12</idno>
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<langUsage>
<language ident="en">English</language>
</langUsage>
<textClass>
<keywords scheme="author">
<term xml:lang="en"> Signal Transduction/immunology</term>
<term xml:lang="en"> Sequence Homology</term>
<term xml:lang="en"> Amino Acid</term>
<term xml:lang="en"> Host-Pathogen Interactions/immunology</term>
<term xml:lang="en"> Humans</term>
<term xml:lang="en"> Immunity</term>
<term xml:lang="en"> Innate</term>
<term xml:lang="en"> Interferon Type I/metabolism</term>
<term xml:lang="en"> Lyssavirus/classification/*genetics/*immunology/pathogenicity</term>
<term xml:lang="en"> Molecular Sequence Data</term>
<term xml:lang="en"> Rabies virus/genetics/immunology/pathogenicity</term>
<term xml:lang="en"> Conserved Sequence</term>
<term xml:lang="en"> Animals</term>
<term xml:lang="en">Amino Acid Sequence</term>
<term xml:lang="en"> Species Specificity</term>
<term xml:lang="en"> STAT Transcription Factors/immunology</term>
<term xml:lang="en"> Viral Proteins/genetics/immunology</term>
</keywords>
<classCode scheme="mesh">Amino Acid Sequence</classCode>
<classCode scheme="mesh">Animals</classCode>
<classCode scheme="mesh">Immunity, Innate</classCode>
<classCode scheme="mesh">Interferon Type I</classCode>
<classCode scheme="mesh">Lyssavirus</classCode>
<classCode scheme="mesh">Molecular Sequence Data</classCode>
<classCode scheme="mesh">Rabies virus</classCode>
<classCode scheme="mesh">STAT Transcription Factors</classCode>
<classCode scheme="mesh">Sequence Homology, Amino Acid</classCode>
<classCode scheme="mesh">Signal Transduction</classCode>
<classCode scheme="mesh">Species Specificity</classCode>
<classCode scheme="mesh">Viral Proteins</classCode>
<classCode scheme="mesh">Conserved Sequence</classCode>
<classCode scheme="mesh">Host-Pathogen Interactions</classCode>
<classCode scheme="mesh">Humans</classCode>
<classCode scheme="halDomain" n="sdv.mp.vir">Life Sciences [q-bio]/Microbiology and Parasitology/Virology</classCode>
<classCode scheme="halTypology" n="ART">Journal articles</classCode>
</textClass>
<abstract xml:lang="en">
<p>The evasion of host innate immunity by Rabies virus, the prototype of the genus Lyssavirus, depends on a unique mechanism of selective targeting of interferon-activated STAT proteins by the viral phosphoprotein (P-protein). However, the immune evasion strategies of other lyssaviruses, including several lethal human pathogens, are unresolved. Here, we show that this mechanism is conserved between the most distantly related members of the genus, providing important insights into the pathogenesis and potential therapeutic targeting of lyssaviruses.</p>
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