Researchers at the University of Illinois Chicago have designed an assay that can be used in at-home tests for rapid COVID-19 screening. Results from an early preclinical study suggest that tests with the new assay may be just as reliable as the laboratory-based PCR tests, according to a news release from the university.
“Having fast and easy-to-use tests for COVID-19 is critical, especially in the communities that have low rates of vaccination and low access to healthcare services, including COVID-19 surveillance and diagnostic testing,” said Xiaowei Wang, UIC Professor of Pharmacology and Bioengineering. “The current crisis has created an unprecedented need for rapid tests that are highly sensitive, and the sooner we can develop better technology and testing options, the better it will be for everyone.”
In laboratory molecular tests, scientists mix samples with assay reagents in a highly controlled process. Because the reaction conditions (like temperature) are tightly controlled, the tests are both sensitive and selective, meaning the chance of false positives or false negatives is very low. However, these laboratory tests can be expensive and are not accessible in all communities and field settings.
The challenge with at-home and field tests is that they need assay reagents to work under less controlled conditions, which increases the chances for false results or inconclusive tests. One method, called loop-mediated isothermal amplification (LAMP), which uses six DNA primers for pathogen detection, has shown promise for other pathogens, like malaria, but has not been efficiently applied to COVID-19.
Wang and the UIC researchers who developed the new COVID-19 assay first created and applied a bioinformatics algorithm to identify the best potential DNA primer combinations for reliably detecting SARS-CoV-2, the virus that causes COVID-19, with the LAMP method. Then, the researchers ran a series of simulations to optimize the conditions under which the potential DNA primer combinations worked best in the field environments.
After using their analysis to develop a testing method using the DNA primers and conditions, the team designed experiments to see how the test performed.
In experiments, Wang and his collaborators processed artificial samples and human samples with a standard PCR test and with their new test. When the results were compared, the researchers not only saw significant improvement in the efficiency of their test over others using the LAMP method to detect the virus but also that it was comparable to more expensive gold standard PCR tests.
Wang said this lab-based study shows that their test works, but that they will need to validate the test in further studies with a greater number of samples from real patients. He hopes that, by summer, they will have conducted a study including about 1,500 patient samples. If the study validates the test, the data will be submitted with an application to U.S. Food and Drug Administration for Emergency Use Authorization.
