Saliva is Comparable to Nasopharyngeal Swabs for Molecular Detection of SARS-CoV-2

The continued need for molecular testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the potential for self-collected saliva as an alternative to nasopharyngeal (NP) swabs for sample acquisition led us to compare saliva to NP swabs in an outpatient setting without restrictio...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Microbiology spectrum 2021-09, Vol.9 (1), p.e0016221-e0016221, Article 00162
Hauptverfasser: Callahan, Cody, Ditelberg, Sarah, Dutta, Sanjucta, Littlehale, Nancy, Cheng, Annie, Kupczewski, Kristin, McVay, Danielle, Riedel, Stefan, Kirby, James E., Arnaout, Ramy
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The continued need for molecular testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the potential for self-collected saliva as an alternative to nasopharyngeal (NP) swabs for sample acquisition led us to compare saliva to NP swabs in an outpatient setting without restrictions to avoid food, drink, smoking, or tooth-brushing. A total of 385 pairs of NP and saliva specimens were obtained, the majority from individuals presenting for initial evaluation, and were tested on two high-sensitivity reverse transcriptase PCR (RT-PCR) platforms, the Abbott m2000 and Abbott Alinity m (both with limits of detection OD] of 100 copies of viral RNA/ml). Concordance between saliva and NP swabs was excellent overall (Cohen's kappa = 0.93) for both initial and follow-up testing, for both platforms, and for specimens treated with guanidinium transport medium as preservative as well as for untreated saliva (kappa = 0.88 to 0.95). Viral loads were on average 16x higher in NP specimens than saliva specimens, suggesting that only the relatively small fraction of outpatients (similar to 8% in this study) who present with very low viral loads (
ISSN:2165-0497
2165-0497
DOI:10.1128/Spectrum.00162-21