New drug target for Ebola, Marburg viruses
Ebola and Marburg are among the most deadly viruses, with mortality rates from these infections ranging from 25% to 90%. While no drugs currently are available on the market to prevent infection from these viruses — they belong to a category of viruses called filoviruses, which are known to cause hemorrhagic fever — researchers have identified a few small drug molecules that can block filoviruses from infecting cells by occupying a single site on a glycoprotein in the virus.
Now, researchers at the University of Illinois Chicago have identified a second site on the filovirus glycoprotein to which small drug molecules can bind and prevent infection. The researchers say that small drug molecules that block both glycoprotein sites may be more effective and reduce the risk of side effects.
These findings are reported in the journal PLOS Pathogens.
“We need to identify how these filoviruses get into cells as a means to help us identify or develop drugs that can prevent infection,” said Lijun Rong, UIC professor of microbiology and immunology at the College of Medicine and a corresponding author of the paper. “Even though at the moment Ebola and Marburg are not in the news that often, having drugs in our arsenal in case of a flare-up is invaluable. These viruses also mutate constantly, so having a better understanding of how they work will let us develop next-generation viral inhibitors.”
Rong’s group and his collaborators, led by Rui Xiong, UIC research assistant professor of pharmaceutical sciences at the College of Pharmacy, identified the second glycoprotein binding site by pairing the virus with hundreds of different small drug molecules thought to possibly have an effect on viral entry into cells. Several of the drugs were able to prevent viral entry.
Through a series of experiments using molecular, biophysical and structural experimental techniques, they were able to look more closely at how these drugs were interacting with the virus. They found that the drugs were binding to a previously unknown site on the viral surface glycoprotein required for cell infection.
“The good news is that there are already drugs approved by the FDA that can bind to the new site we identified,” Rong said. “If we can give drugs that bind to the site we newly identified and the site previously identified, it can help prevent viral infection with lower doses of each drug. Interfering with both sites on the viral surface glycoprotein, it also reduces the chances of the glycoprotein mutating to the point that it escapes the effect of the drug combination and is able to infect cells once again.”
Xiong is also a corresponding author of the paper. Adam Schafer, Laura Cooper, Raghad Nowar, Hyun Lee, Yangfeng Li, Benjamin Ramirez, Michael Caffrey, Han Cheng of UIC; Norton Peet of Chicago BioSolutions, Inc.; Erica Ollmann Saphire of the LaJolla Institute of Immunology, and Gregory Thatcher, formerly of UIC and now of the University of Arizona, are co-authors on the paper.
This research was partially supported by grant awards from the National Institutes of Health (R41AI12697, R42 AI126971).
Written by Sharon Parmet