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Evaluation of Specimen Types and Saliva Stabilization Solutions for SARS-CoV-2 Testing
Sara B Griesemer1, Greta Van Slyke1, Dylan Ehrbar1
1Division of Infectious Diseases, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Journal of Clinical Microbiology
|March 6, 2021
Summary
Nasopharyngeal swabs for COVID-19 testing are scarce. Combining nasal swabs and saliva offers improved SARS-CoV-2 detection sensitivity, with saliva remaining stable for days without special solutions.
Area of Science:
- Virology
- Infectious Diseases
- Diagnostic Testing
Background:
- Accurate SARS-CoV-2 detection is vital for pandemic control.
- Nasopharyngeal swabs (NPS), the gold standard for COVID-19 testing, face supply chain challenges.
- Alternative specimen types like nasal swabs (NS) and saliva are being explored for easier collection and reduced exposure.
Purpose of the Study:
- To compare the diagnostic sensitivity of nasal swabs (NS) and saliva against nasopharyngeal swabs (NPS) for SARS-CoV-2 detection.
- To evaluate the combined detection sensitivity of nasal swabs and saliva.
- To assess the stability of SARS-CoV-2 virus in saliva.
Main Methods:
- Matched nasopharyngeal swabs, nasal swabs, and saliva specimens were collected from two outpatient cohorts (n=463).
- SARS-CoV-2 detection was performed using RT-PCR.
- Spiking experiments and virus stability assays at different temperatures were conducted.
Main Results:
- SARS-CoV-2 detection sensitivity was 97.9% for NPS, 87.1% for NS, and 87.1% for saliva in the second cohort (41% positivity).
- Combining nasal swabs and saliva achieved 94.6% detection sensitivity.
- SARS-CoV-2 remained stable in saliva for up to 7 days at 4°C and room temperature; stabilizing solutions did not improve stability.
Conclusions:
- While NS and saliva show reduced sensitivity compared to NPS, their combination improves detection rates.
- Saliva is a stable specimen for SARS-CoV-2 testing without the need for special transport solutions.
- Further assessment is needed to determine the clinical acceptability of reduced sensitivity for NS and saliva in specific settings.
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