Every year as mosquito season arrives, West Nile virus causes fever in thousands of people and life-threatening brain infections in an unlucky few.
About half the people who survive that infection, West Nile encephalitis, are left with permanent neurological deficits such as memory loss.
New research shows that these long-term neurological problems may be due to the patient’s own immune system destroying parts of the neurons in the brain. The findings suggest that intervening in the immune response may help prevent brain damage so patients can recover.
West Nile was first identified in the Western Hemisphere in 1999, when groups of birds began dying in New York and a veterinary pathologist at the Bronx Zoo brought the deaths to the attention of the Centers for Disease Control and Prevention. The virus has since spread throughout the Americas, infecting millions of people.
Long-term Neurological Problems
Ten thousand West Nile survivors are living with long-term neurological problems such as fatigue, weakness, difficulty walking, and memory loss, and the number goes up by about 1,000 every year following mosquito season. There is no vaccine or specific treatment for West Nile infection.
“When I talk with other doctors about West Nile patients with these persistent neurological deficits, many say, ‘The virus in their brains must have killed neurons, and there’s nothing we can do about it,’”
says senior author Robyn Klein, professor of medicine at Washington University in St. Louis.
“My thinking has been, if we can determine what triggers this brain damage, maybe we can prevent it from happening or stop it afterwards.”
Robyn Klein, MD, PhD, and Michael Vasek, PhD, examine images of mouse synapses. The researchers found that memory loss suffered by some survivors of West Nile encephalitis may be caused by the loss of synapses between neurons. (Photo: Robert Boston/School of Medicine)
For the study, researchers developed a mouse model of West Nile encephalitis by injecting a weakened strain of the virus directly on top of the mouse hippocampus, a region of the brain important for memory. A month after the mice had recovered from the infection, the researchers tested their ability to navigate a maze.
Microglial Cells On Fire
Much like West Nile survivors who cannot navigate their neighborhoods, the infected mice couldn’t remember how to navigate the maze. But contrary to conventional wisdom, their hippocampal neurons hadn’t been killed by the virus.
Instead, the researchers found that microglial cells, a kind of immune cell that lives in the brain, were clustered around the neurons at the site of infection and were highly activated—”on fire,” as Klein put it.
Moreover, levels of an immune protein called complement were high in the brains of mice with memory loss. Neurons make connections to each other at junctions called synapses, allowing information to be passed from cell to cell.
During normal brain development, many more synapses are formed than needed and only those that are strengthened should persist. Complement tags the weak synapses to be removed, and the activated microglia destroy them.
In the mice with memory loss, viral infection seemed to have sent this system into overdrive, leading to the destruction of necessary synapses. Synapses must be formed or strengthened for learning and memory to occur. While the neurons near the activated microglia were still alive, they lacked synapses.
The more synapses that were destroyed, the worse the mouse’s memory problems.
“There’s never been any model of cognitive dysfunction due to brain infection that shows that eliminating synapses without loss of neurons could cause these symptoms,”
says Klein, who is also a professor of pathology and immunology, and of neuroscience.
“It’s really a paradigm-shifting idea that a viral infection can do this. It also makes us wonder whether these mechanisms are involved in other diseases associated with memory loss.”
Healthy people create new synapses throughout life as they learn new things. West Nile survivors, however, may be unable to grow new synapses to replace the ones lost during their bouts of encephalitis.
“The microglia remain activated long after the virus is cleared, and this may be preventing the synapses from recovering,” Klein says “But that gives us hope that we can develop interventions directed at the immune response. We think we can treat this, and that’s what we’re trying to do.”
The National Institutes of Health funded the work.
Michael J. Vasek, Charise Garber, Denise Dorsey, Douglas M. Durrant, Bryan Bollman, Allison Soung, Jinsheng Yu, Carlos Perez-Torres, Arnaud Frouin, Daniel K. Wilton, Kristen Funk, Bette K. DeMasters, Xiaoping Jiang, James R. Bowen, Steven Mennerick, John K. Robinson, Joel R. Garbow, Kenneth L. Tyler, Mehul S. Suthar, Robert E. Schmidt, Beth Stevens & Robyn S. Klein A complement–microglial axis drives synapse loss during virus-induced memory impairment Nature 534, 538–543 (23 June 2016) doi:10.1038/nature18283
Image: CDC/ P.E. Rollin. Transmission electron micrograph (TEM) of the West Nile virus.