COVID-19 can be Better Diagnosed from Saliva


The study team included samples from a hospital and nursing home as well as from a drive-through testing site. In the first phase (protocol U), 240 matched NPS and saliva sample pairs were tested prospectively for SARS-CoV-2 RNA by RT-PCR.

‘Saliva can be more efficient than nasopharyngeal swabs for COVID-19 testing. The addition of a simple processing step to saliva samples before testing may enhance the COVID-19 detection rate, reduce the challenges of nasopharyngeal testing, and promote mass surveillance.’


In the second phase of the study (SalivaAll), 189 matched pairs, including 85 that had been previously evaluated with protocol U, were processed in an Omni bead mill homogenizer (an innovative protocol designed by the team for higher sensitivity than NPS) before RT-PCR testing.

Saliva Sample Vs. Nasopharyngeal Swab

Also, additional studies were conducted to confirm the clinical sensitivity in NPS samples. It was found that in Phase I, 28.3% of samples tested positive for SARS-CoV-2 from either NPS, saliva, or both. The detection rate was lower in saliva compared to NPS (50.0% vs. 89.7%).

Whereas, in Phase II, 50.2% of samples tested positive for SARS-CoV-2 from saliva, NPS, or both. The detection rate was higher in saliva compared to NPS samples (97.8 % vs. 78.9%).

The detection rate was 100% for samples tested with SalivaAll and 36.7% with protocol U among the 85 saliva samples tested. The study thereby successfully validated saliva samples in the five-sample pooling strategy.

The team speculated that the gel-like consistency of saliva samples contributed to the lower sensitivity of saliva to RT-PCR testing. Thus adding the homogenization step rendered the saliva samples to attain uniform viscosity and consistency and made it easier to perform the assay.

“Monitoring SARS-CoV-2 will remain a public health need. The use of a non-invasive collection method and easily accessible sample such as saliva will enhance screening and surveillance activities and bypass the need for sterile swabs, expensive transport media, and exposure risk, and even the need for skilled healthcare workers for sample collection,” says lead investigator Ravindra Kolhe, MD, Ph.D., Department of Pathology, Medical College of Georgia, Augusta University, Augusta, GA, USA.

Source: Medindia



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