Membrane Traffic Pathways in Viral Replication and Pathogenesis
Lead Research Organisation:
University College London
Department Name: UNLISTED
Abstract
Whether direct infections of man or infections that impact on domestic animals, crops or the environment in general, virus infections are a major health and economic burdens for mankind. Viruses require cells for infection and replication. Understanding the various ways in which viruses gain entry to cells, exploit cellular mechanisms for their replication and exert their pathogenic potential is key to intervening in these processes. Our work aims to understand aspects of the cell biology of human immunodeficiency viruses (HIV), the infectious agents associated with AIDS, and the arboviruses Dengue virus and Semliki Forest virus, representatives of two families of viruses transmitted by mosquitoes and currently responsible for wide-spread epidemics in the tropics. We will focus on understanding how a set of cellular proteins can prevent specific events in the entry of these viruses into cells, with a view to exploiting these proteins as natural inhibitors of infection. In parallel, we aim to use knowledge acquired over many years to identify broad-spectrum, small molecule, inhibitors of arbovirus infection that can be used as prophylactics or in epidemic situations. We will continue current work on virus assembly, using new methods to understand the cell biology of virus formation and, for HIV in particular, how modification of key signals in viral proteins, required for correct virus assembly, impact on viral pathogenesis.
Technical Summary
The mechanisms used by viruses to invade and replicate in cells are of fundamental interest, both in terms of improved understanding of infection and pathogenesis, with implications for health and economic wellbeing, but also because viruses are extraordinary tools for revealing how cells work. Because they have membranes, we are focussed on understanding how enveloped viruses interact with cellular membrane systems, how these interactions facilitate or restrict the transmission of viruses from cell to cell and how they impact on pathogenesis. We are developing these themes through existing and new programs of work with the aim of exploiting our current know-how to develop knowledge-based interventions against viral infection and/or pathogenesis. In new programs of work, we are investigating (1) how interferon-induced transmembrane (IFITM) proteins inhibit the entry of a broad range of enveloped viruses, (2) the potential to develop broad-spectrum antivirals that inhibit the entry of viruses that exploit the same endocytic entry mechanisms, and (3) the cell biological processes underlying virus particle formation.
The work focuses on three new projects developed during the previous QQ. The program synergises with the programs of other MRC LMCB groups, in particular those of Mercer, who is also interested in the cell biology of viral replication, Henriques, with whom we are developing new methods for investigating virus-cell interactions using advanced imaging methods, and Paluch, Cutler, Pichaud, Stefan and Baum, with whom we will collaborate to develop understanding of the mechanisms through which viruses that assemble at the cell surface deform the membrane and overcome the barrier imposed by the cortical cytoskeleton.
Our main objectives are:
1.To determine the molecular mechanism(s) through which IFITM proteins inhibit enveloped virus entry.
2.To use and expand our understanding of arboviruses to develop novel broad-spectrum antivirals.
3.To use novel imaging techniques to further develop our understanding of how HIV and related viruses assemble at the plasma membrane, and to gain insight into how the physical properties of the plasma membrane and cortical cytoskeleton impact on these events.
The work focuses on three new projects developed during the previous QQ. The program synergises with the programs of other MRC LMCB groups, in particular those of Mercer, who is also interested in the cell biology of viral replication, Henriques, with whom we are developing new methods for investigating virus-cell interactions using advanced imaging methods, and Paluch, Cutler, Pichaud, Stefan and Baum, with whom we will collaborate to develop understanding of the mechanisms through which viruses that assemble at the cell surface deform the membrane and overcome the barrier imposed by the cortical cytoskeleton.
Our main objectives are:
1.To determine the molecular mechanism(s) through which IFITM proteins inhibit enveloped virus entry.
2.To use and expand our understanding of arboviruses to develop novel broad-spectrum antivirals.
3.To use novel imaging techniques to further develop our understanding of how HIV and related viruses assemble at the plasma membrane, and to gain insight into how the physical properties of the plasma membrane and cortical cytoskeleton impact on these events.
People |
ORCID iD |
Mark Marsh (Principal Investigator) |
Publications
Bednarska J
(2020)
Rapid formation of human immunodeficiency virus-like particles.
in Proceedings of the National Academy of Sciences of the United States of America
Benfield CT
(2020)
Correction: Bat IFITM3 restriction depends on S-palmitoylation and a polymorphic site within the CD225 domain.
in Life science alliance
Benfield CT
(2020)
Bat IFITM3 restriction depends on S-palmitoylation and a polymorphic site within the CD225 domain.
in Life science alliance
Griffiths G
(2022)
Nanoparticle entry into cells; the cell biology weak link
in Advanced Drug Delivery Reviews
Lawrence SP
(2022)
A cellular trafficking signal in the SIV envelope protein cytoplasmic domain is strongly selected for in pathogenic infection.
in PLoS pathogens
Llorente García I
(2020)
A biophysical perspective on receptor-mediated virus entry with a focus on HIV.
in Biochimica et biophysica acta. Biomembranes
Mazzon M
(2019)
Identification of Broad-Spectrum Antiviral Compounds by Targeting Viral Entry.
in Viruses
Mazzon M
(2018)
Alphavirus-induced hyperactivation of PI3K/AKT directs pro-viral metabolic changes.
in PLoS pathogens
Related Projects
Project Reference | Relationship | Related To | Start | End | Award Value |
---|---|---|---|---|---|
MC_UU_00012/1 | 01/04/2017 | 31/03/2022 | £1,079,000 | ||
MC_UU_00012/2 | Transfer | MC_UU_00012/1 | 01/04/2017 | 31/03/2022 | £989,000 |
MC_UU_00012/3 | Transfer | MC_UU_00012/2 | 01/04/2017 | 31/03/2022 | £925,000 |
MC_UU_00012/4 | Transfer | MC_UU_00012/3 | 01/04/2017 | 31/03/2022 | £908,000 |
MC_UU_00012/5 | Transfer | MC_UU_00012/4 | 01/04/2017 | 31/03/2022 | £1,560,000 |
MC_UU_00012/6 | Transfer | MC_UU_00012/5 | 01/04/2017 | 31/03/2022 | £1,234,000 |
MC_UU_00012/7 | Transfer | MC_UU_00012/6 | 01/04/2017 | 31/03/2022 | £1,070,000 |
Description | Role of SIV and HIV Env cytoplasmic tail in pathogenesis and protective immunity |
Amount | £276,611 (GBP) |
Funding ID | 1RO1A/138782-01 |
Organisation | National Institutes of Health (NIH) |
Sector | Public |
Country | United States |
Start | 07/2018 |
End | 06/2022 |
Description | Env trafficking signals in SIV pathogenesis |
Organisation | University of Pennsylvania |
Department | Perelman School of Medicine |
Country | United States |
Sector | Academic/University |
PI Contribution | Cell biological analysis of the role of trafficking signals in the cytoplasmic domain of the simian immunodeficiency virus envelope protein - a model for understanding HIV pathogenesis and anti-viral immune responses. |
Collaborator Contribution | Virological and in vivo studies that complement the cell biology. |
Impact | Nine publications Multi-disciplinary: Virology, cell biology, in vivo animal models |
Description | Open day/Science Fair |
Form Of Engagement Activity | Participation in an open day or visit at my research institution |
Part Of Official Scheme? | No |
Type Of Presentation | Workshop Facilitator |
Geographic Reach | Regional |
Primary Audience | Public/other audiences |
Results and Impact | An open day/science fair for MRC funded researchers at UCL - LMCB a principle host and organiser. 500 members of public attended and took part in lectures, demonstrations and other events. Part of MRC Centenary celebrations. Significant feedback from public impressed by presentations and visibility of MRC funded research. |
Year(s) Of Engagement Activity | 2013 |
URL | http://www.ucl.ac.uk/lmcb/lmcb-takes-lead-mrc-centenary-celebrations-ucl |