Murine gamma herpesvirus 68 hijacks MAVS and IKKβ to abrogate NFκB activation and antiviral cytokine production

Xiaonan Dong, Pinghui Feng

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

Upon viral infection, mitochondrial antiviral signaling (MAVS) protein serves as a key adaptor to promote cytokine production. We report here that murine gamma herpesvirus 68 (γHV68), a model virus for oncogenic human gamma herpesviruses, subverts cytokine production via the MAVS adaptor. During early infection, γHV68 hijacks MAVS and IKKβ to induce the site-specific phosphorylation of RelA, a crucial subunit of the transcriptionally active NFκB dimer, which primes RelA for the proteasome-mediated degradation. As such, γHV68 efficiently abrogated NFκB activation and cytokine gene expression. Conversely, uncoupling RelA degradation from γHV68 infection promoted NFκB activation and elevated cytokine production. Loss of MAVS increased cytokine production and immune cell infiltration in the lungs of γHV68-infected mice. Moreover, exogenous expression of the phosphorylation- and degradation-resistant RelA variant restored γHV68-induced cytokine production. Our findings uncover an intricate strategy whereby signaling via the upstream MAVS adaptor is intercepted by a pathogen to nullify the immediate downstream effector, RelA, of the innate immune pathway.

Original languageEnglish (US)
Article numbere1002336
JournalPLoS Pathogens
Volume7
Issue number11
DOIs
StatePublished - Nov 2011

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Rhadinovirus
Herpesviridae
Antiviral Agents
Cytokines
Phosphorylation
Herpesviridae Infections
Oncogenic Viruses
Virus Diseases
Proteasome Endopeptidase Complex
Gene Expression
Lung
Infection

ASJC Scopus subject areas

  • Microbiology
  • Parasitology
  • Virology
  • Immunology
  • Genetics
  • Molecular Biology

Cite this

Murine gamma herpesvirus 68 hijacks MAVS and IKKβ to abrogate NFκB activation and antiviral cytokine production. / Dong, Xiaonan; Feng, Pinghui.

In: PLoS Pathogens, Vol. 7, No. 11, e1002336, 11.2011.

Research output: Contribution to journalArticle

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