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PLoS Pathog. 2010 Jul 29;6(7):e1001001. doi: 10.1371/journal.ppat.1001001.

Murine gamma-herpesvirus 68 hijacks MAVS and IKKbeta to initiate lytic replication.

Author information

1
Department of Microbiology, UT Southwestern Medical Center, Dallas, Texas, USA.

Abstract

Upon viral infection, the mitochondrial antiviral signaling (MAVS)-IKKbeta pathway is activated to restrict viral replication. Manipulation of immune signaling events by pathogens has been an outstanding theme of host-pathogen interaction. Here we report that the loss of MAVS or IKKbeta impaired the lytic replication of gamma-herpesvirus 68 (gammaHV68), a model herpesvirus for human Kaposi's sarcoma-associated herpesvirus and Epstein-Barr virus. gammaHV68 infection activated IKKbeta in a MAVS-dependent manner; however, IKKbeta phosphorylated and promoted the transcriptional activation of the gammaHV68 replication and transcription activator (RTA). Mutational analyses identified IKKbeta phosphorylation sites, through which RTA-mediated transcription was increased by IKKbeta, within the transactivation domain of RTA. Moreover, the lytic replication of recombinant gammaHV68 carrying mutations within the IKKbeta phosphorylation sites was greatly impaired. These findings support the conclusion that gammaHV68 hijacks the antiviral MAVS-IKKbeta pathway to promote viral transcription and lytic infection, representing an example whereby viral replication is coupled to host immune activation.

PMID:
20686657
PMCID:
PMC2912392
DOI:
10.1371/journal.ppat.1001001
[Indexed for MEDLINE]
Free PMC Article

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