Saliva Test Image
Stored in orange-capped vials for mass distribution, the DRUL buffer is part of an inexpensive saliva-based COVID test developed at Rockefeller. (Credit: Rockefeller University)

In the early days of the pandemic, with commercial COVID tests in short supply, researchers at Rockefeller University developed an in-house assay to identify positive cases within the Rockefeller community. It turned out to be easier and safer to administer than the tests available at the time, and it has been used tens of thousands of times over the past nine months to identify and isolate infected individuals working on the university’s campus.

Now, a new study confirms that the test performs as well, if not better, than FDA-authorized nasal and oral swab tests. In a direct head-to-head comparison of 162 individuals who received both Rockefeller’s “DRUL” saliva test and a conventional swab test, DRUL caught all of the cases that the swabs identified as positive — plus four positive cases that the swabs missed entirely.

The DRUL test offered several advantages. It was safe — a test that could be taken at home and sent to the lab in transport medium that kills virus on contact. It was efficient. The assay used only off-the-shelf reagents, ducking beneath shortages that felled other programs. It was inexpensive, costing around $2 per test.

The researchers first assessed DRUL’s limit of detection—how many viral copies the test could catch per volume of fluid. The test succeeded in detecting a single viral particle in one microliter of saliva, a figure comparable to that of the most sensitive assays. The lab then ran 30 nasal swabs that had tested positive for COVID-19 through their novel testing platform. DRUL caught all 30.

Next, in a direct challenge, the team compared 162 results from volunteers who received both a swab and a saliva test. Predictably, almost all came back negative. But four that were negative or indeterminate on the swab test were positive on the DRUL assay and, indeed, three of those samples belonged to volunteers who went on to develop symptomatic COVID.