Today, most COVID-19 conversation is about the when and where of the vaccine. But the country’s public health experts have been clear—now is not the time to take our foot off the gas when it comes to testing. Continued access to affordable, reliable testing is essential.
That is why the new COVID-19 test, developed by a team of researchers at the University of Rhode Island, is so important. Because it is saliva-based, URI’s test is less invasive than many of the traditional nasal swab tests, and our researchers say it is sensitive, specific, and can deliver results at a lower cost.
The University is launching a clinical trial this week as part of the final phase of data collection and validation in preparation for an Emergency Use Authorization submission to the U.S. Food and Drug Administration. And URI students will play a part.
The trial, conducted in cooperation with URI Athletics and URI Health Services, will test student-athletes and others who consent to take part, with the data collected to be included as part of the University’s application to the FDA. The University has established a lab on its Kingston Campus expressly for the trial. The effort is a partnership between URI’s College of Pharmacy and the URI Research Foundation, with financial support from the URI President’s Office and a $100,000 gift from John ’87 and Sheila Priore for the testing lab.
Less invasive, more accessible test
“One of the things we set out to do was to develop a less invasive, more cost-effective, more accessible test,” said Slitt. “And I think we’ve done that. We use saliva, work off different supply chains, use different, less cost-prohibitive instrumentation, and are effectively lowering the barriers to entry for many.”
Led by Professor of Biomedical and Pharmaceutical Sciences Angela Slitt, the team began working on the test, which uses branched DNA assay technology, last spring when access to the more common polymerase chain reaction (PCR) tests was severely hampered due to disruptions in the supply chain. Although PCR-based tests receive high marks for their sensitivity, they also require extraction of the nucleic acids, access to thermocyclers and other sophisticated lab equipment not as readily available outside of the United States.
Slitt was already using her research in URI’s Sources, Transport, Exposure, and Effects of PFASs (STEEP) lab, funded by the National Institutes of Health Superfund Research program, to look at changes in genetic material when the idea hit her. Since her PFAS test is ultimately used to look at these changes using branched DNA assay technology more commonly available in labs throughout the United States, she reasoned that this research could be adapted to identify coronavirus in human saliva samples.
With the Rhode Island Department of Health, the team has validated the assay using standard reference materials and specimens. The team is also working with Thermo Fisher Scientific, of Waltham, Massachusetts, to validate the test and provide the necessary supply chain for distribution.
Now in the final stretch of data collection to apply for FDA Emergency Use Authorization, Slitt believes the team’s COVID-19 test will be one of the few assay tests that could be made globally available. Based on trials conducted thus far, the test appears to have a high level of sensitivity similar to or more sensitive than other top-performing saliva tests on the market—meaning the test is better able to comparably detect the level of viral load in the sample. This is particularly helpful in gauging infectivity and possibility for spread.
“From start to finish this has been an extraordinary team effort drawing on expertise and support from across the University, as well as from the Rhode Island Department of Health and experts in industry, to protect our students and make a positive impact for others,” said URI President David M. Dooley. “The development of the test and the lab really speak to our mission as a research university engaged in relevant work that affects people’s lives.”
FDA approval of the test for diagnostic purposes would have far-reaching implications, both at home and abroad, in terms of increasing accessibility to testing to help manage pandemic response. In Rhode Island, FDA approval of the test would mean that it could be made widely available for surveillance and risk assessment on URI’s campuses, to local colleges and universities, as well as to schools across the state to assist in monitoring and testing for the coronavirus. Outside of the United States it could have a profound impact.
Says Slitt, “With minimal scientific equipment, we can not only increase our capacity in the United States but also help to put tools into the hands of people in developing countries that they can use.”