Completed Infection & Immunity Genetics & Molecular Biology

Characterisation of host virus interactions.

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AI plain-English summary

HIV-1, the virus that causes most AIDS cases, has evolved to slip past a human protein called tetherin that would otherwise trap and disable it. This project will map exactly how HIV-1 and related viruses evade this and other innate immune defences. The problem is that while some lentiviruses—a family that includes HIV—only infect certain primates without causing widespread disease, HIV-1 M has become a global pandemic. Researchers suspect that differences in how these viruses interact with human restriction factors determine which ones can spread. But the molecular details remain poorly understood, especially for tetherin, the most recently discovered restriction factor. This is fundamental science. The team will combine molecular biology, structural studies, and evolutionary analysis to reveal how host proteins dictate which viruses can infect humans. They will also search for entirely new restriction factors in human macrophages, the immune cells that HIV targets. Understanding these molecular handshakes could eventually inform strategies to block viral entry or boost natural defences. Past discoveries of restriction factors have already led to insights for antiviral drug design, though any practical applications from this work remain years away.

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We aim to extend our knowledge of innate immune restriction factors and define the molecular details of the relationships between restriction factors and their viral encoded targets and antagonists. We aim to test the hypothesis that innate restriction has played a role in limiting the spread of non-pandemic lentiviruses in humans. We will also examine how pandemic HIV-1 M avoids restriction, focusing on tetherin as the most recently discovered and least well defined factor. Our work will consid er how HIV-1 avoids triggering innate responses in human macrophages as well as seeking novel restriction factors in these cells. We will also examine whether non-primate lentiviruses and herpesviruses are restricted by tetherin and how they antagonise it. Finally, we will consider the enhancement of HIV-1 replication by cyclophilin A using a hypersensitive mutant as well as considering a role for cyclophilins in nuclear import. We expect this work to reveal details of lentiviral nuclear entry. Overall, we aim to combine molecular studies with phylogenetic, biophysics and structural studies to define the role of host factors in determining viral tropism.

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Researchers

Greg Towers (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

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The role of Vpu and tetherin in HIV/AIDS pathogenesis
Studying lentiviruses to understand mechanisms, regulation and consequences of nucleic acid sensing
Host and Viral Determinants of Interferon Resistance During HIV-1 Transmission
Analysis of how specific RNA motifs in HIV-1 and lentiviral vector genomes control infectious virus production

Original classification

Senior Research Fellowship Basic Renewal

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