Completed Infection & Immunity Genetics & Molecular Biology

Adaptation of avian influenza virus polymerase to humans during pandemic emergence.

In plain English

AI plain-English summary

Bird flu viruses must mutate their polymerase machinery to replicate inside human cells, and this project will map exactly how that happens. The problem is clear: avian influenza viruses occasionally jump to humans, causing severe illness, but they cannot spread efficiently between people until they adapt. The viral polymerase—the enzyme that copies the virus’s genetic material—is the main barrier. The researcher recently identified a host protein, ANP32A, that differs between birds and mammals and blocks avian polymerase activity in human cells. This project will uncover how ANP32A supports viral replication, identify other host factors that restrict or permit the polymerase, and measure how polymerase mutation rates change during adaptation. If successful, this work will explain why partially adapted bird viruses trigger a destructive immune overreaction—the cytokine storm—in infected people. That knowledge could guide development of antiviral drugs and improve pandemic preparedness plans by revealing which viral mutations signal an emerging pandemic threat. The research is fundamental science: it asks how a virus evolves to switch hosts. But understanding that process is what allows public health agencies to spot dangerous strains before they spread.

View original technical description
Influenza viruses cause intermittent pandemics and seasonal outbreaks that affect millions of humans every year. My goal is to chart the adaptation of influenza virus to the human host from emergence from birds, often associated with severe infections, to endemicity as a seasonal flu virus. I will focus on the viral polymerase because it is a key determinant of host range, pathogenicity and viral evolution. Using next generation sequencing we will establish accurate quantification of the viral polymerase error rate to test whether polymerase constellation determines pandemic potential. Polymerase interacts with a plethora of host proteins, some permissive and others that restrict it. We recently discovered a key host factor, ANP32A, that differs between birds and mammals and explains the major barrier to avian influenza virus polymerase activity in humans. We will uncover the mechanism by which this host factor supports viral replication using a combination of familiar and novel techniques. We will also discover other species-specific host factors that act on polymerase to support or restrict it. Finally, we will explain why partially adapted avian viruses lead to a devastating cytokine storm in humans they infect, as this may guide therapeutic options and inform pandemic preparedness plans.

View the original record at the funder ↗

Researchers

Wendy Barclay (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Rapid acquisition of mammalian characteristics by avian influenza virus in single host infections.
Structure-function relationships of the influenza virus RNA polymerase: influence on virulence, host restriction and innate immune responses
Investigating the role of ANP32A in the replication of Avian Influenza Virus
Understanding the Molecular Features of Novel Emergent (H9Nx and H7Nx) Avian Influenza Viruses Posing Zoonotic and Pandemic Threats
Influenza polymerase interaction with its host transcriptional partners

Original classification

Investigator Award in Science

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