The Murine Gammaherpesvirus Immediate-Early Rta Synergizes with IRF4, Targeting Expression of the Viral M1 Superantigen to Plasma Cells

• Type of Material: Article
• Authors: Brigid M. O'Flaherty, Emory University; Tanushree Soni, Emory University; Brian Wakeman, Emory University; Sam Speck, Emory University
• Language: English
• Date: 2014-08
• Publisher: Public Library of Science
• Publication Version: Final Published Version
• Copyright Statement: © 2014 O'Flaherty et al.
• Final Published Version (URL): http://www.plospathogens.org/article/info%3Adoi%2F10.1371%2Fjournal.ppat.1004302
• Title of Journal or Parent Work: PLoS Pathogens
• ISSN: 1553-7366
• Volume: 10
• Issue: 8
• Start Page: e1004302
• End Page: e1004302
• Grant/Funding Information: This research was supported by NIH R01 AI073830.
• Research Categories: Biology, Microbiology; Biology, Virology; Health Sciences, Immunology

Abstract

MHV68 is a murine gammaherpesvirus that infects laboratory mice and thus provides a tractable small animal model for characterizing critical aspects of gammaherpesvirus pathogenesis. Having evolved with their natural host, herpesviruses encode numerous gene products that are involved in modulating host immune responses to facilitate the establishment and maintenance of lifelong chronic infection. One such protein, MHV68 M1, is a secreted protein that has no known homologs, but has been shown to play a critical role in controlling virus reactivation from latently infected macrophages. We have previous demonstrated that M1 drives the activation and expansion of Vβ4+ CD8+ T cells, which are thought to be involved in controlling MHV68 reactivation through the secretion of interferon gamma. The mechanism of action and regulation of M1 expression are poorly understood. To gain insights into the function of M1, we set out to evaluate the site of expression and transcriptional regulation of the M1 gene. Here, using a recombinant virus expressing a fluorescent protein driven by the M1 gene promoter, we identify plasma cells as the major cell type expressing M1 at the peak of infection in the spleen. In addition, we show that M1 gene transcription is regulated by both the essential viral immediate-early transcriptional activator Rta and cellular interferon regulatory factor 4 (IRF4), which together potently synergize to drive M1 gene expression. Finally, we show that IRF4, a cellular transcription factor essential for plasma cell differentiation, can directly interact with Rta. The latter observation raises the possibility that the interaction of Rta and IRF4 may be involved in regulating a number of viral and cellular genes during MHV68 reactivation linked to plasma cell differentiation.