Just as flu season swings into full gear, researchers from the 抖阴旅行射 Boulder and University of Texas at Austin have uncovered a previously unknown mechanism by which the human immune system tries to battle the influenza A virus. The discovery sheds new light on how the virus鈥攚hich kills 12,000 to 56,000 people in the United States annually鈥攐ften wins, and it could ultimately lead to new treatments.
A student gets a flu shot on the 抖阴旅行射 Boulder campus. A new study reveals how the body attempts to fight flu on its own听and why it often loses.
鈥淲e鈥檝e solved a mystery, revealing a new aspect of our innate immune system and what flu has to do to get around it,鈥� says Nicholas Meyerson, a postdoctoral researcher in the BioFrontiers Institute and lead author of a paper .
The findings, several years in the making, could lead to a better understanding of how the seasonal flu virus, which typically originates in birds, makes its way to humans. They could also inform development of next-generation antivirals able to combat a broad spectrum of influenza strains, says co-senior author Robert Krug, a leading influenza researcher and professor at the University of Texas at Austin.
The paper focuses on two key molecular players in the story of influenza infection: a human protein called TRIM25, which was recently discovered to play an important role in the human immune response to flu infection,听and a protein called NS1, present in all strains of the influenza A virus and shown to bind TRIM25 to keep it from doing its job.
鈥淲e were basically trying to find out what TRIM25 was doing that flu did not want it to be doing and the role NS1 was playing in blocking that function,鈥� Krug said.
Through a series of laboratory tests, the team revealed two main findings:
TRIM25 acts earlier than previously believed, latching on to a critical and unique flu virus structure like a 鈥渕olecular clamp鈥� to keep the virus from replicating as soon as TRIM25 detects this unique structure.
NS1 produced by the flu virus can block this function of TRIM25, enabling flu to circumvent the immune response and cause infection.
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Previous research had suggested TRIM25 fought off flu by switching on what is known as the 鈥渋nterferon response鈥濃�攁 complex signaling pathway that arms cells through the body to fight off pathogens. But not all strains of influenza block this interferon signaling pathway, which led Meyerson to suspect another mechanism was at play in helping TRIM25 fight flu.
The paper reveals TRIM25 is also a 鈥渞estriction factor,鈥� a special protein present in the fastest-acting arm of the immune system, before spreading infection occurs.
鈥淩estriction factors lie in wait,听and, should a virus be detected in one of your cells, they have immediate destructive ability,鈥� explains co-senior author Sara Sawyer, an associate professor of Molecular, Cellular and Developmental Biology (MCDB) at 抖阴旅行射 Boulder.
Flu uses its NS1 protein to evade TRIM25鈥檚 early flu-fighting response, the researchers found.
To do the study, the researchers first infected transgenic cell lines loaded with nonhuman primate versions of TRIM25 with the human influenza A virus. They found that the cells fought off the virus far better than human versions of the TRIM25 protein.
鈥淭his told us that TRIM25 has the capacity to crush influenza, but that its human form was less active,鈥� Meyerson said.
Postdoctoral researcher Nicholas Meyerson
To find out how it crushes influenza, the researchers combined purified TRIM25 with purified viral ribonucleoproteins (vRNPs)鈥� eight-piece protein chains that house the influenza genome鈥攁nd used state-of-the-art electron microscopy to take pictures of what happened.They found that TRIM25 appears to swiftly recognize the unique structure of vRNPs and clamps down on them to keep them from replicating inside the cell. Other experiments confirmed the NS1 protein in flu virus inhibits this function.
They also found that TRIM25 (previously believed to be present only in the cell cytoplasm) is also present in the cell nucleus, which is the same cellular location where flu replication occurs.
Sawyer and Meyerson are now looking to further investigate the role TRIM25 plays in cross-species transmission of influenza.
More studies are needed, but Krug believes new therapeutics could be designed to block the NS1 protein produced by the flu virus, hobbling its ability to evade the human immune system.
鈥淚f you could somehow block NS1 from acting, you could block all strains of the virus,鈥� he says.
