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Publication : The gammaherpesvirus 68 viral cyclin facilitates expression of LANA.

First Author  Niemeyer BF Year  2021
Journal  PLoS Pathog Volume  17
Issue  11 Pages  e1010019
PubMed ID  34780571 Mgi Jnum  J:315187
Mgi Id  MGI:6830806 Doi  10.1371/journal.ppat.1010019
Citation  Niemeyer BF, et al. (2021) The gammaherpesvirus 68 viral cyclin facilitates expression of LANA. PLoS Pathog 17(11):e1010019
abstractText  Gammaherpesviruses establish life-long infections within their host and have been shown to be the causative agents of devastating malignancies. Chronic infection within the host is mediated through cycles of transcriptionally quiescent stages of latency with periods of reactivation into detectable lytic and productive infection. The mechanisms that regulate reactivation from latency remain poorly understood. Previously, we defined a critical role for the viral cyclin in promoting reactivation from latency. Disruption of the viral cyclin had no impact on the frequency of cells containing viral genome during latency, yet it remains unclear whether the viral cyclin influences latently infected cells in a qualitative manner. To define the impact of the viral cyclin on properties of latent infection, we utilized a viral cyclin deficient variant expressing a LANA-beta-lactamase fusion protein (LANA::betala), to enumerate both the cellular distribution and frequency of LANA gene expression. Disruption of the viral cyclin did not affect the cellular distribution of latently infected cells, but did result in a significant decrease in the frequency of cells that expressed LANA::betala across multiple tissues and in both immunocompetent and immunodeficient hosts. Strikingly, whereas the cyclin-deficient virus had a reactivation defect in bulk culture, sort purified cyclin-deficient LANA::betala expressing cells were fully capable of reactivation. These data emphasize that the gammaHV68 latent reservoir is comprised of at least two distinct stages of infection characterized by differential LANA expression, and that a primary function of the viral cyclin is to promote LANA expression during latency, a state associated with ex vivo reactivation competence.
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