Although largely asymptomatic, human cytomegalovirus (HCMV) can cause severe and even fatal disease in a subset of susceptible individuals. While great progress has been made in understanding essential stages of HCMV replication, a detailed description of many of these processes is lacking. Of particular interest in this proposal is cytoplasmic envelopment. To provide a molecular description of the events associated with cytoplasmic envelopment, it is important to identify the factors involved, both viral and cellular. Previous work has identified UL71 as an envelopment factor that potentially mediates membrane scission, as viruses lacking UL71 are trapped at various stages of budding. It is not known whether UL71 is sufficient itself for promoting scission or if it requires other viral and/or cellular factors. Many viruses utilize cellular machinery known as the endosomal sorting complexes required for transport (ESCRTs) as part of the envelopment process. While HCMV does not require the early ESCRT-I complex, it does require the late ESCRT Vps4. The role of the ESCRT-III complex, which is the major driver of membrane deformation and scission promoter, has not yet been investigated. Understanding the role, if any, for ESCRT-III during infection is essential for providing a detailed description of cytoplasmic envelopment. We hypothesize that UL71 recruits ESCRT-III and Vps4 to mediate scission of budding HCMV capsids. In support of this hypothesis, an interaction between UL71 and Vps4 has been reported. The experiments in this proposal will investigate if ESCRT-III subunits are required for HCMV replication, and if so at what stage. They will investigate the relationship, if any, between UL71 and ESCRT-III and define a function for the UL71-Vps4 interaction, as well as identify regions on UL71 important for function. These studies will further our understanding of the contribution of cellular factors to HCMV infection and potentially identify novel ways in which viral replication can be targeted. Taken together, these studies will lay the foundation for a mechanistic understanding of HCMV cytoplasmic envelopment.

Public Health Relevance

HCMV is a ubiquitous virus found throughout all geographic regions and socioeconomic groups that has severe clinical implications when infection occurs in immunocrompromised individuals and pregnant women. This project seeks to elucidate the molecular details of the capsid envelopment step during virus assembly, with a focus on both the viral and cellular factors involved. These studies will provide both important information regarding the viral life cycle and elucidate potentially novel ways in which viral replication can be targeted therapeutically.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI130156-01
Application #
9288293
Study Section
Virology - A Study Section (VIRA)
Program Officer
Beisel, Christopher E
Project Start
2017-07-17
Project End
2022-06-30
Budget Start
2017-07-17
Budget End
2018-06-30
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Pennsylvania State University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
129348186
City
Hershey
State
PA
Country
United States
Zip Code
17033
Streck, Nicholas T; Carmichael, Jillian; Buchkovich, Nicholas J (2018) A non-envelopment role for the ESCRT-III complex during HCMV infection. J Virol :