دورية أكاديمية
The varicella-zoster virus ORF47 kinase interferes with host innate immune response by inhibiting the activation of IRF3.
| العنوان: | The varicella-zoster virus ORF47 kinase interferes with host innate immune response by inhibiting the activation of IRF3. |
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| المؤلفون: | Vandevenne, Patricia, Lebrun, Marielle, El Mjiyad, Nadia, Ote, Isabelle, Di Valentin, Emmanuel, Habraken, Yvette, Dortu, Estelle, Piette, Jacques, Sadzot-Delvaux, Catherine |
| المساهمون: | Giga-Signal Transduction - ULiège |
| المصدر: | PLoS ONE, 9 (2) (2011-02) |
| بيانات النشر: | Public Library of Science |
| سنة النشر: | 2011 |
| المجموعة: | University of Liège: ORBi (Open Repository and Bibliography) |
| مصطلحات موضوعية: | Varicella zoster virus, Innate immunity, Life sciences, Biochemistry, biophysics & molecular biology, Sciences du vivant, Biochimie, biophysique & biologie moléculaire |
| الوصف: | peer reviewed ; The innate immune response constitutes the first line of host defence that limits viral spread and plays an important role in the activation of adaptive immune response. Viral components are recognized by specific host pathogen recognition receptors triggering the activation of IRF3. IRF3, along with NF-kappaB, is a key regulator of IFN-beta expression. Until now, the role of IRF3 in the activation of the innate immune response during Varicella-Zoster Virus (VZV) infection has been poorly studied. In this work, we demonstrated for the first time that VZV rapidly induces an atypical phosphorylation of IRF3 that is inhibitory since it prevents subsequent IRF3 homodimerization and induction of target genes. Using a mutant virus unable to express the viral kinase ORF47p, we demonstrated that (i) IRF3 slower-migrating form disappears; (ii) IRF3 is phosphorylated on serine 396 again and recovers the ability to form homodimers; (iii) amounts of IRF3 target genes such as IFN-beta and ISG15 mRNA are greater than in cells infected with the wild-type virus; and (iv) IRF3 physically interacts with ORF47p. These data led us to hypothesize that the viral kinase ORF47p is involved in the atypical phosphorylation of IRF3 during VZV infection, which prevents its homodimerization and subsequent induction of target genes such as IFN-beta and ISG15. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| تدمد: | 1932-6203 |
| العلاقة: | urn:issn:1932-6203; https://orbi.uliege.be/handle/2268/103006Test; info:hdl:2268/103006; https://orbi.uliege.be/bitstream/2268/103006/1/Vandevenne.pdfTest; scopus-id:2-s2.0-79951801158; info:pmid:21347389 |
| DOI: | 10.1371/journal.pone.0016870 |
| الإتاحة: | https://doi.org/10.1371/journal.pone.0016870Test https://orbi.uliege.be/handle/2268/103006Test https://orbi.uliege.be/bitstream/2268/103006/1/Vandevenne.pdfTest |
| حقوق: | open access ; http://purl.org/coar/access_right/c_abf2Test ; info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.90070FF9 |
| قاعدة البيانات: | BASE |
Full Text Finder | تدمد: | 19326203 |
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| DOI: | 10.1371/journal.pone.0016870 |