Familiar drugs may block Ebola virus infection
Lijun Rong, professor of microbiology and immunology. Photo: Jenny Fontaine/UIC Office of Public Affairs (click on image for larger file size)
A well-known class of molecules, many of which are already in use therapeutically, may be able to block the Ebola virus’s entry into cells and halt the disease in its tracks, according to researchers at the University of Illinois at Chicago.
The study is available online in advance of print in the Journal of Virology.
Ebola and the closely related Marburg virus are among the most lethal in the world, both highly contagious and deadly. There is an urgent need to develop either a vaccine or effective antiviral therapy to prevent future outbreaks.
“We know very little about the basic biology of these diseases,” said Lijun Rong, UIC professor in microbiology and immunology and principal investigator on the new study.
Rong and his colleagues found that Ebola and Marburg viruses both use gateways called G protein-coupled receptors, or GPCRs, to enter a cell after attaching to its surface. Blocking entry with a drug that ties up the receptor may prove to be an effective therapy.
“These G protein-coupled receptors are a big family of closely related molecules in humans — altogether, probably more than a thousand,” said Rong. Because GPCRs are involved in many human diseases, he said, a host of drugs have already been developed that target them.
“In the history of therapeutics, about half of our drugs were developed to target GPCRs. For example, a number of antihistamines used as allergy medications are GPCR receptor antagonists,” he said.
Rong and his coworkers screened approximately a thousand compounds using a NIH-funded high-throughput screening facility. They found 20 GPCR antagonists, or molecules that block GPCR receptors, were able to block Ebola and Marburg viruses from entering cells.
Learning how the two viruses infect cells and how they can be blocked offers the hope of finding therapeutics to combat both deadly diseases, Rong said.
“There are a lot of drugs and compounds that work through this mechanism — acting as antagonists to GPCR receptors,” he said. “This gives us a huge repertoire that can be tested against Ebola/Marburg.”
UIC postdoctoral research associate Han Cheng is first author on the study. Co-authors are UIC graduate student Elizabeth Varhegyi and UIC professor of microbiology and immunology Zheng W. Chen; Calli Lear-Rooney and Gene Olinger of the U.S. Army Medical Research Institute of Infectious Diseases at Fort Detrick, Maryland; and Lisa Johansen of Horizon Discovery, Inc., in Cambridge, Massachusetts.
This research was partially supported by National Institutes of Health grant AI77767. USAMRIID efforts were supported by Defense Threat Reduction Agency project 4.10007_08_RD_B and subcontract W81XWH-08-0051. Opinions, interpretations, conclusions, and recommendations are those of the authors and are not necessarily endorsed by the U.S. Army.
