New RNA-Based Breath Test to Detect COVID-19 More Predictive of Lower Respiratory Tract Involvement

Researchers have developed a unique method for detecting SARS-CoV-2 in breath samples using viral RNA detection.

A team of researchers at Brown University (Providence, RI, USA) has created a breathalyzer device that reverse-transcribes RNA from airborne virus particles into DNA, which can then be tested for COVID-19 via a common PCR test. The device, dubbed the Bubbler, uses an enzymatic reaction mixture to detect viral RNA and convert it to DNA, where it can be measured using a PCR instrument. The Bubbler can also barcode that DNA, allowing a sample to be linked directly to the patient it came from and be used for sequencing.

The Bubbler is a glass tube with a glass pipette into which patients exhale. The tube is filled with a reverse transcription reaction mixture and cold mineral oil. The name of the device comes from the bubbling sound that occurs when the patient exhales into the device. In the study, 70 patients were screened and samples from three points in the respiratory tract were tested: Saliva obtained from tongue scrapes in the mouth and samples of 15 seconds of exhaled breath collected in the Bubbler were compared to a conventional nasopharyngeal swab PCR test.

The study determined that SARS-CoV-2 can be readily detected in the breath and is more predictive of lower respiratory tract involvement. Viral RNA is more enriched in the breath relative to oral samples, while oral samples include cells involved with SARS-CoV-2 replication that breath samples do not. This suggests the viral signal detected in the Bubbler comes from active viral particles. Tests for COVID-19 usually use samples collected from the upper respiratory tract by saliva or nasopharyngeal swab. Positive samples contain active virus, but viral load in the upper respiratory tract is not correlated with symptoms in the lower respiratory tract, such as pneumonia.

Virus detection by the Bubbler is similar to a hospital-swab PCR test. However, because swab tests detect viral RNA fragments in cells that persist in previously infected cells, PCR tests can return a positive result for months after infection. By contrast, the Bubbler detects airborne viral particles and is a better measure of risk of contagion. It can also be adapted for environmental sampling in hospitals, transportation hubs and closed environments like offices, ships and planes. The barcode returns a viral sequence that also supports strain identification, which may prove useful as more information is learned about transmissibility and possible strain-specific treatment decisions. It can also be used for simultaneous batches of pooled samples, provides additional information such as viral load and strain identity, and eliminates the need for stabilizing a sample, potentially allowing the assay to be performed at home.

The investigators also demonstrated how the Bubbler might be adapted to detect virus in airborne samples. To model the movement of droplets exhaled in human breath, three unique nucleic acid samples were added to three personal humidifiers at different locations at varied distances from the Bubbler in a room with high airflow and a room with low airflow. Although a detailed exploration of this application was beyond the scope of the study, the results demonstrate the potential to use aerosolized nucleic acids to quantitatively map airflow in indoor spaces, and to detect SARS-CoV-2 in the air.

“The Bubbler is more likely to be a better indicator of current infection than nasopharyngeal swabs,” said lead investigator William G. Fairbrother, a professor in the Department of Molecular Biology, Cell Biology and Biochemistry at Brown. “Involvement of the lower respiratory tract is often a precursor to severe COVID-19, so there is an argument for a more direct sampling focused on exhaled breath.”

Related Links:
Brown University