Flaviviruses impact a large proportion of the world's population. West Nile virus is the most prevalent mosquito transmitted pathogen in North America, with infected patients at risk of developing severe neurological disease. Dengue virus is a related virus, with more than 400 million infections worldwide every year. There is currently no vaccine or treatment available for either virus. A new discovery from the University of Alberta's Faculty of Medicine & Dentistry could open the door to one day treat or prevent diseases caused by West Nile virus and Dengue virus infections.
The research, published and featured in the Spot Light section of the Journal of Virology, examines a previously unknown connection between flaviviruses, a classification of viruses that include West Nile virus, Dengue virus and tick-borne encephalitis virus, and organelles (a specialized subunit within a cell) known as peroxisomes that help coordinate the body's immune responses. Postdoctoral fellow Jaehwan You and Shangmei Hou, the lead authors on the study, found that flaviviruses induce degradation of a protein called Pex19, which is essential for the building of new peroxisomes, setting off a chain reaction that could leave the body more vulnerable to viral infection.
‘Loss of peroxisomes results in the loss of the ability of the cells to produce an interferon that inhibits replication of viruses. This finding could open new avenues to treat or prevent diseases caused by West Nile virus and Dengue virus infections.’
AdvertisementTom Hobman, senior author and professor of cell biology, said, "Peroxisomes, as it turns out, are required for production of an antiviral molecule called interferon lambda. Interferon lambda is produced by infected cells and has been shown to inhibit replication of multiple viruses. We hypothesized that loss of peroxisomes results in the loss of the ability of the cells to produce this interferon, which indeed was found to be the case. It looks like the virus may be targeting peroxisomes to prevent antiviral defense by the cell."
The study found that in infected cells, about 35% of the peroxisomes had disappeared. Production of interferon was also down by approximately 80%. Richard Rachubinski, a study co-author and one of the world's leading authorities on peroxisomes, said, "While the team set out to find how viruses manipulate host cells, the link to peroxisomes was completely unexpected. You can't plan this. You just cannot. It goes to show the unexpected avenues one finds in discovery research that you'd never anticipate."
According to the researchers, this latest work may now open new possibilities for intervention in flavivirus infection.
Hobman said, "It's certainly within the realm of possibility that if peroxisomes play this key role in antiviral defense, it may be possible to take drugs that are known to boost peroxisome production to provide protection against the viruses."
The researchers think it likely that other viruses may also target peroxisomes in a similar manner to flaviviruses. They hope to now show it through new studies which are currently underway.
Hobman said, "I think we're just at the tip of the iceberg. No one has ever really thought about viruses and peroxisomes before. Now I think there is going to be a flood of work in this field."