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Comparison of RT-PCR and antigen test sensitivity across nasopharyngeal, nares, and oropharyngeal swab, and saliva sample types during the SARS-CoV-2 omicron variant.

Authors :
Damhorst GL
Lin J
Frediani JK
Sullivan JA
Westbrook A
McLendon K
Baugh TJ
O'Sick WH
Roback JD
Piantadosi AL
Waggoner JJ
Bassit L
Rao A
Greenleaf M
O'Neal JW
Swanson S
Pollock NR
Martin GS
Lam WA
Levy JM
Source :
Heliyon [Heliyon] 2024 Feb 29; Vol. 10 (6), pp. e27188. Date of Electronic Publication: 2024 Feb 29 (Print Publication: 2024).
Publication Year :
2024

Abstract

Limited data highlight the need to understand differences in SARS-CoV-2 omicron (B.1.1.529) variant viral load between the gold standard nasopharyngeal (NP) swab, mid-turbinate (MT)/anterior nasal swabs, oropharyngeal (OP) swabs, and saliva. MT, OP, and saliva samples from symptomatic individuals in Atlanta, GA, in January 2022 and longitudinal samples from a small familial cohort were tested by both RT-PCR and ultrasensitive antigen assays. Higher concentrations in the nares were observed in the familial cohort, but a dominant sample type was not found among 39 cases in the cross-sectional cohort. The composite of positive MT or OP assay for both RT-PCR and antigen assay trended toward higher diagnostic yield but did not achieve significant difference. Our data did not identify a singular preferred sample type for SARS-CoV-2 testing, but higher levels of saliva nucleocapsid, a trend toward higher yield of composite OP/MT result, and association of apparent MT or OP predominance with symptoms warrant further study.<br />Competing Interests: The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Wilbur Lam, Greg Martin reports financial support was provided by 10.13039/100000070National Institute of Biomedical Imaging and Bioengineering. Wilbur Lam, Greg Martin reports administrative support was provided by 10.13039/100006108National Center for Advancing Translational Sciences. This research was supported by funds from the NIDCD Division of Intramural Research to Joshua Levy (DC000097).

Details

Language :
English
ISSN :
2405-8440
Volume :
10
Issue :
6
Database :
MEDLINE
Journal :
Heliyon
Publication Type :
Academic Journal
Accession number :
38500996
Full Text :
https://doi.org/10.1016/j.heliyon.2024.e27188