Enteroviruses are among the most severe causes of human disease, and recent outbreaks of emerging enteroviruses such as types D68 and 71 have highlighted the need to understand more about these pathogens. Our comparative studies of poliovirus (PV), coxsackievirus B3, and now EV-D68 have shown many commonalities in the life-cycles of these viruses. We have focused our studies on how members of the Enterovirus genus trigger a cellular pathway known as autophagy to promote production of infectious virus. Autophagy is a constitutive degradative cellular process required for turnover of damaged vesicles, aggregated proteins, and other spent cellular components. During times of stress, including amino acid starvation, organismal development, and infection, autophagy is up-regulated. Autophagic vesicles, thought to be derived from the complex web of viral RNA replication membranes, can be observed during mid-to-late infection. We and others have demonstrated that viral proteins specifically induce autophagic signaling and autophagosome formation. These autophagosomes acidify, promoting maturation of the viral capsid and release of newly formed infectious viruses, often encased in these cell-derived membranes, from the cell. In this proposal, we outline a comprehensive plan to understand generation of membranes during infection, from the initial RNA replication membranes to the autophagosomes promoting maturation of virions to the single-membraned virus- containing vesicles being released from the cell. Understanding this entire pathway, the latter parts of which have only been identified within the past few years, will provide an understanding of how these viruses replicate, mature, release from cells, and evade immune detection.
In Specific Aim I, we will analyze how specific viral non-structural proteins initiate autophagosome formation at the early stages of infection and regulate downstream steps in autophagosome formation, acidic maturation, and virus release.
In Specific Aim II, we will investigate the viral and host requirements for development of viral RNA replication membranes, and the mechanism of formation of autophagosomes from these convoluted membrane structures, during infection. These experiments can be carried out in the absence of host proteins from the autophagic pathway and other cellular pathways. In addition, we have shown that acidic autophagosomes promote maturation of the virion by inducing cleavage of the capsid protein VP0 into VP2 and VP4. We propose a biochemical approach to identifying the factor(s) contained within autophagosomes required for infectious maturation of viral capsids. There is a major research gap in understanding development of enterovirus-induced membranes, from the initial signals sent by virus proteins at the beginning of infection, to the release of virus-containing vesicles. This proposal will address that need by investigating each step in this pathway from beginning - initiation of RNA replication membranes - to end - the release of virus-containing vesicles.

Public Health Relevance

Picornaviruses are a major cause of several diverse human diseases, and this project will analyze how model picornaviruses, including poliovirus, coxsackievirus B3, and enterovirus D68, interact with their cellular environments. In particular we want to understand how cell membranes are physically rearranged to promote the creation of infectious virions. We expect the results of this study to lead to development of therapeutics targeting virus-generated membranes and membrane proteins, to prevent replication and spread of infectious virus.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI104928-08
Application #
10023149
Study Section
Virology - A Study Section (VIRA)
Program Officer
Park, Eun-Chung
Project Start
2013-06-01
Project End
2024-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
8
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Maryland Baltimore
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
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Corona, Abigail K; Jackson, William T (2018) Finding the Middle Ground for Autophagic Fusion Requirements. Trends Cell Biol 28:869-881
Rajput, Charu; Han, Mingyuan; Bentley, J Kelley et al. (2018) Enterovirus D68 infection induces IL-17-dependent neutrophilic airway inflammation and hyperresponsiveness. JCI Insight 3:
Corona, Abigail K; Saulsbery, Holly M; Corona Velazquez, Angel F et al. (2018) Enteroviruses Remodel Autophagic Trafficking through Regulation of Host SNARE Proteins to Promote Virus Replication and Cell Exit. Cell Rep 22:3304-3314
Klionsky, Daniel J (see original citation for additional authors) (2016) Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy 12:1-222
Sidjanin, D J; Park, Anna K; Ronchetti, Adam et al. (2016) TBC1D20 mediates autophagy as a key regulator of autophagosome maturation. Autophagy 12:1759-1775
Jackson, William T (2015) Viruses and the autophagy pathway. Virology 479-480:450-6
Rosenthal, Ann K; Gohr, Claudia M; Mitton-Fitzgerald, Elizabeth et al. (2015) Autophagy modulates articular cartilage vesicle formation in primary articular chondrocytes. J Biol Chem 290:13028-38
Richards, Alexsia L; Soares-Martins, Jamária A P; Riddell, Geoffrey T et al. (2014) Generation of unique poliovirus RNA replication organelles. MBio 5:e00833-13
Jackson, William T (2014) Poliovirus-induced changes in cellular membranes throughout infection. Curr Opin Virol 9:67-73