Lytic promoter activity during herpes simplex virus latency is dependent on genome location
Year: 2024
Type: article
Abstract: ABSTRACT Herpes simplex virus 1 (HSV-1) is a significant pathogen that establishes lifelong latent infections with intermittent episodes of resumed disease. In mouse models of HSV infection, sporadic low-level lytic gene expression has been detected during latency in the absence of reactivation events that lead to production of new viruses. This viral activity during latency has been reported using a sensitive Cre-marking model for several lytic gene promoters placed in one location in the HSV-1 genome. Here, we extend these findings in the same model by examining first, the activity of an ectopic lytic gene promoter in several places in the genome and second, whether any promoters might be active in their natural context. We found that Cre expression was detected during latency from ectopic and native promoters, but only in locations near the ends of the unique long genome segment. This location is significant because it is in close proximity to the region from which latency-associated transcripts (LATs) are derived. These results show that native HSV-1 lytic gene promoters can produce protein products during latency, but that this activity is only detectable when they are located close to the LAT locus. IMPORTANCE HSV is a significant human pathogen and the best studied model of mammalian virus latency. Traditionally, the active (lytic) and inactive (latent) phases of infection were considered to be distinct, but the notion of latency being entirely quiescent is evolving due to the detection of some lytic gene expression during latency. Here, we add to this literature by finding that the activity can be found for native lytic gene promoters as well as for constructs placed ectopically in the HSV genome. However, this activity was only detectable when these promoters were located close by a region known to be transcriptionally active during latency. These data have implications for our understanding of HSV gene regulation during latency and the extent to which transcriptionally active regions are insulated from adjacent parts of the viral genome.
Source: Journal of Virology
DOI: 10.1128/jvi.01258-24
Institution: Australian National University
Language: English
Subfield: Infectious Diseases
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Funders: Australian Government, Curtin University of Technology, Department of Education, Australian Governement, Department of Health and Aged Care, Australian Government, Department of Education and Training, Medical Research Council, Australian Research Council, National Health and Medical Research Council
Awards: The cellular basis of sex-specific responses to virus infection, G2341276394, G314337482, Reducing the burden of DNA viruses on human health, A proteome-wide approach to anti-viral immunity and vaccine development, G5872327945, G6005848514, G7002453265, Understanding the role of ongoing viral activity in herpes simplex virus latency, G8104795072
OpenAlex ID: W4403604932