Pathogenic Old and New World arenaviruses cause severe hemorrhagic fever in humans. There are currently no approved vaccines or drugs to battle arenavirus infection. Despite intensive studies, arenavirus entry pathways into host cells and the mechanism of arenavirus glycoprotein (GP) mediated virus-cell fusion are not well understood. Old World and New World arenaviruses use distinct cellular receptors and poorly characterized endocytic pathways to enter and infect cells. Based on our preliminary data and published work, we propose a novel overarching hypothesis that Old and New World arenaviruses use common post-uptake pathways to enter a subset of late endosomes that contain a specific lipid cofactor, LBPA, but lack the host restriction factor IFITM3. We found that fusion of diverse arenaviruses is promoted by LBPA and that the Lassa virus bypasses endosomes enriched in IFITM3, thereby escaping restriction. We also found that GP-mediated fusion requires thiol-disulfide interchange within this glycoprotein and obtained evidence that GP mediates arenavirus membrane permeabilization prior to fusion with acidic endosomes, which we hypothesized promotes subsequent virus uncoating. The following four Specific Aims will test the above hypotheses. (1) Delineate the entry pathways of representative Old and New World arenaviruses, using real-time single pseudovirus imaging. (2) Define the role of LBPA in arenavirus fusion and identify the GP lipid-interacting motif. (3) Examine the requirement for GP thiol-disulfide interchange in arenavirus fusion. (4) Elucidate a role of GP-mediated virus membrane permeabilization in uncoating. Successful completion of the proposed experiments will provide important fundamental insights into the mechanism of arenavirus entry/fusion and identify new therapeutic targets for intervention.

Public Health Relevance

Pathogenic arenaviruses, such as Lassa and Junin viruses, cause severe hemorrhagic fever in humans. No specific antivirals or an FDA-approved vaccine are available against these pathogens. To inform new therapeutic strategies, we propose to delineate the entry pathways of Old and New World arenaviruses into cells and identify key intermediate steps of the viral fusion process that initiates infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
2R01AI053668-18
Application #
9755767
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Dupuy, Lesley Conrad
Project Start
2003-09-15
Project End
2024-02-29
Budget Start
2019-03-08
Budget End
2020-02-29
Support Year
18
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Emory University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Sood, Chetan; Francis, Ashwanth C; Desai, Tanay M et al. (2017) An improved labeling strategy enables automated detection of single-virus fusion and assessment of HIV-1 protease activity in single virions. J Biol Chem 292:20196-20207
Desai, Tanay M; Marin, Mariana; Mason, Caleb et al. (2017) pH regulation in early endosomes and interferon-inducible transmembrane proteins control avian retrovirus fusion. J Biol Chem 292:7817-7827
Hampton, Cheri M; Strauss, Joshua D; Ke, Zunlong et al. (2017) Correlated fluorescence microscopy and cryo-electron tomography of virus-infected or transfected mammalian cells. Nat Protoc 12:150-167
Oum, Yoon Hyeun; Desai, Tanay M; Marin, Mariana et al. (2016) Click labeling of unnatural sugars metabolically incorporated into viral envelope glycoproteins enables visualization of single particle fusion. J Virol Methods 233:62-71
Markosyan, Ruben M; Miao, Chunhui; Zheng, Yi-Min et al. (2016) Induction of Cell-Cell Fusion by Ebola Virus Glycoprotein: Low pH Is Not a Trigger. PLoS Pathog 12:e1005373
Padilla-Parra, Sergi; Marin, Mariana; Kondo, Naoyuki et al. (2014) Pinpointing retrovirus entry sites in cells expressing alternatively spliced receptor isoforms by single virus imaging. Retrovirology 11:47
Matos, Pedro M; Marin, Mariana; Ahn, Byungwook et al. (2013) Anionic lipids are required for vesicular stomatitis virus G protein-mediated single particle fusion with supported lipid bilayers. J Biol Chem 288:12416-25
Padilla-Parra, Sergi; Marin, Mariana; Gahlaut, Nivriti et al. (2013) Fusion of mature HIV-1 particles leads to complete release of a gag-GFP-based content marker and raises the intraviral pH. PLoS One 8:e71002
Padilla-Parra, Sergi; Matos, Pedro M; Kondo, Naoyuki et al. (2012) Quantitative imaging of endosome acidification and single retrovirus fusion with distinct pools of early endosomes. Proc Natl Acad Sci U S A 109:17627-32
Padilla-Parra, Sergi; Marin, Mariana; Kondo, Naoyuki et al. (2012) Synchronized retrovirus fusion in cells expressing alternative receptor isoforms releases the viral core into distinct sub-cellular compartments. PLoS Pathog 8:e1002694

Showing the most recent 10 out of 17 publications