Glucose-Based Test Detects Range of COVID Variants

Now, that information could be right at their fingertips, literally. A team of scientists has found a way to use common glucose meters, like the ones that many people with diabetes use, to measure the level of COVID-19 antibodies a person has in their blood. Antibodies are proteins created in response to a disease, and remain in the body to fight the next encounter.

Currently, to get a COVID-19 antibody test, people have to get their blood drawn at a health care facility. But scientists at Johns Hopkins University (Baltimore, MD, USA) wanted to create a test that was more affordable, accessible and easy to use that would also help people and policymakers make more informed decisions about mask-wearing, booster vaccinations and public safety measures. They chose a glucose meter as the detection device because many pharmacies across the country sell them fairly inexpensively, unlike the expensive equipment many health care facilities must use to measure antibody levels. It also gives a digital readout, making the results easy to interpret.

The scientists are trying to simplify the test for commercial use. But the process aligns closely with how people with diabetes use the glucose meter. The researchers coated the “spike” protein from SARS-CoV-2, the virus that causes COVID-19, onto a glucose monitoring test strip that they designed. The first step is to add a drop of blood to the strip. Spike protein-targeted antibodies from the blood then bind to the strip. Next, the strip is dipped into an enzyme bath, where the enzymes and antibodies bind. Then, the strip is dipped into a new solution full of the sugar sucrose, and the enzyme breaks the sucrose down into glucose. Finally, the glucose meter tests for glucose, which is proportional to the level of COVID-19 antibodies.

In the past, glucose meters have been studied as a means for measuring other chemicals besides sugar. But previous studies ran into a common problem. The challenge was to make a protein that could simultaneously measure the number of antibodies and convert the signal into glucose, so it could then be measured by the glucose meter. To do this, they merged the antibody and enzyme chemically, but the efficiency of the process was too low to be scalable to population-level screening. Instead of merging the two proteins chemically, the team realized they needed to merge them genetically into a new protein.

In a recent study, the researchers tested serum samples from at least six people who had COVID-19 and were undergoing treatment and at least six people who tested negative for the virus. The team found that the glucose-based test was on par with the gold-standard detection method used at health care facilities, pharmacies and testing sites, specifically the enzyme-linked immunosorbent assay (ELISA). The investigators tested the same samples with the glucose monitor test and the industry standard test. They observed a 95% positive and a 96% negative agreement. This means the two tests showed very similar results when testing for samples that were positive and negative for COVID-19.

The researchers have obtained a provisional patent and are reaching out to biotechnology companies to commercialize the technology. However, the researchers want to see what else the glucose-based test can do first. The test not only works for a range of COVID variants but also, potentially, for any disease that produces antibodies in the blood. All they need to do is switch the disease’s correlating protein on the test strip. The team is planning on doing additional studies to simplify the test’s process and analyze its versatility.

“We created something new, something that is not biologically existent in the world right now,” said Netz Arroyo, Ph.D., assistant professor of pharmacology and molecular sciences, one of the inventors of the new approach. “We still think we can improve the reagent and do more with it, and so a part of the process we’re undergoing right now is to see if we can make it even better. And the better we make the reagent, the more commercial interest we’ll get.”

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Johns Hopkins University