PUBLIC RELEASE: 26-FEB-2015
Research published in Science finds new cellular factor critical to Ebola virus infection, discovered small molecule that inhibits virus entry into cell
TEXAS BIOMEDICAL RESEARCH INSTITUTE
SAN ANTONIO (February 26, 2015) – New research that focuses on the mechanism by which Ebola virus infects a cell and the discovery of a promising drug therapy candidate is being published February 27, 2015, in the journal Science. Dr. Robert Davey, scientist and Ewing Halsell Scholar in the Department of Immunology and Virology at Texas Biomedical Research Institute announced today that a small molecule called Tetrandrine derived from an Asian herb has shown to be a potent small molecule inhibiting infection of human white blood cells in vitro or petri dish experiments and prevented Ebola virus disease in mice.
The latest outbreak of Ebola virus disease has caused the death of more than 9,400 people worldwide and created an international crisis that has shown few signs of stopping, continuing to infect thousands in West Africa. Ebola virus causes hemorrhagic fever in humans and currently has no approved therapy or vaccine. Scientists at Texas Biomed have been working in the Institute’s Biosafety Level 4 containment laboratory for more than 10 years to find a vaccine, therapies and detection methods for the virus.
Davey and his team have been working for more than five years on identifying and finding therapy targets for Ebola virus disease. Davey’s research has focused on stopping the virus before it has a chance to enter or interact with cellular factors, as that is a critical first step to combatting infection.
Ebola virus begins its entry into a cell by first binding to several types of cell surface proteins. Then the virus is taken into the cell and follows an endosomal route, or membrane-bound route that transports the virus to various cell compartments.
From previous studies, Davey said that during this endosomal process, he knew that calcium signaling in cells, which allow cells to transmit electrical charges to one another, controls many of the processes in the cell and was important for Ebola virus infection.
“We were not able, however, to pinpoint the mechanisms involved in this process,” Davey explained. “With this research, we discovered that two pore channels (TPCs) are the key calcium sensor involved in Ebola virus infection. These TPCs essentially need to be turned on in order for the virus to function properly.”
Two pore channels are unusual calcium channels found in endosomes that control the way endosomes move through cells and the environment of the cells. Davey compared TPCs to traffic cops and air conditioners, helping direct the endosomes and any virus it might be carrying through the cell and making the endosomes and its passengers more comfortable along the way.
Davey and his team were able to show the critical role of two pore channels in Ebola virus infection, which has not previously been shown in any other virus.
In addition to identifying this critical mechanism to infection, Davey’s team also showed that drugs targeting this interaction show some efficacy as potential treatments against Ebola virus disease.
In the study, Davey’s team determined that existing drugs currently used to treat high blood pressure have an ability to turn this key calcium sensor on and off. Working with a group in Munich, Germany and Southwest Research Institute, the team tested several small molecules to see which was most effective at turning the sensors off thus prohibiting Ebola virus from moving any further through the cell.
The team found Tetrandrine protected mice from disease without obvious side effects and was the best candidate for further animal testing, because it was the most potent compound tested, gave little evidence of cytotoxicity and required a smaller dose to be effective and tolerated.
“When we tested in mice, the drugs stopped virus replication and saved most of them from disease,” Davey said.
Essentially, this drug shows an ability to stop the virus before it has a chance interact with cellular factors, thus stopping the virus from continuing its infection process.
“We are very excited about the progress made in this study and the momentum it provides as scientists across the world vigorously search for effective vaccines and treatments against Ebola virus,” Davey said. “We are cautiously optimistic. The next step in the process is to test both safety and effectiveness of the interaction of the drug with Ebola virus in non-human primates.”
Collaborators and Co-authors on the Science paper include Andrey Kolokoltsov at the University of Texas Medical Branch at Galveston. A team at the Center for Integrated Protein Science Munich (CIPSM) at the Department of Pharmacy – Center for Drug Research at Ludwig-Maximilians-Universität München in Munich, Germany did special cell analysis. That team includes Cheng-Chang Chen, Christian Grimm, Christian Wahl-Schott and Martin Biel. Also contributing is Norbert Klugbauer who previously worked with two pore channels at the Institute for Experimental and Clinical Pharmacology and Toxicology at Albert-Ludwigs-Universität Freiburg in Freiburg, Germany. And, Michael Tidwell and William Bauta performed chemical synthesis at the Southwest Research Institute in San Antonio, Texas.
Texas Biomed, formerly the Southwest Foundation for Biomedical Research, is one of the world’s leading independent biomedical research institutions dedicated to advancing health worldwide through innovative biomedical research. The Institute is located on a 200-acre campus on the northwest side of San Antonio, Texas. Texas Biomed partners with hundreds of researchers and institutions around the world to develop vaccines and therapeutics against viral pathogens causing AIDS, hepatitis, herpes, hemorrhagic fevers and parasitic diseases responsible for malaria, schistosomiasis and Chagas disease. The Institute also has programs in the genetics of cardiovascular disease, diabetes, obesity, psychiatric disorders and other diseases. For more information on Texas Biomed, go to http://www.TxBiomed.org.