Evidence map›Paper›PMID 39246012›Full record

ArticleThe journal of applied laboratory medicine2024

SARS-CoV-2 Variants May Affect Saliva RT-PCR Assay Sensitivity.

Jason S Chwa, Yunho Shin, Yesun Lee, Thomas Fabrizio, Zion Congrave-Wilson, Wesley A Cheng, Jaycee Jumarang, Minjun Kim, Richard Webby, Jeffrey M Bender and 1 more

Abstract read
In one paragraph

Article in The journal of applied laboratory medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Jason S ChwaKeck School of Medicine, University of Southern California, Los Angeles, California, United States.
Yunho ShinDivision of Infectious Diseases, Children's Hospital Los Angeles, Los Angeles, California, United States.ORCID 0009-0001-3934-8544
Yesun LeeDivision of Infectious Diseases, Department of Pediatrics, University of California, San Diego, California, United States.
Thomas FabrizioDepartment of Infectious Diseases, St Jude Children's Research Hospital, Memphis, Tennessee, United States.
Zion Congrave-WilsonDivision of Infectious Diseases, Children's Hospital Los Angeles, Los Angeles, California, United States.
Wesley A ChengDivision of Infectious Diseases, Department of Pediatrics, University of California, San Diego, California, United States.
Jaycee JumarangDivision of Infectious Diseases, Department of Pediatrics, University of California, San Diego, California, United States.
Minjun KimDivision of Infectious Diseases, Department of Pediatrics, University of California, San Diego, California, United States.ORCID 0009-0006-5755-6837
Richard WebbyDepartment of Infectious Diseases, St Jude Children's Research Hospital, Memphis, Tennessee, United States.
Jeffrey M BenderDepartment of Pediatrics, City of Hope Comprehensive Cancer Center, Duarte, California, United States.
Pia S PannarajDivision of Infectious Diseases, Department of Pediatrics, University of California, San Diego, California, United States.

Funding

NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00016 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI WEBBY, RICHARD · 2021 to 2025
$91.4M
Household Respiratory Virus SARS-CoV-2 Transmission and Immunity Sub-Study (HRTS)U01AI144616 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GORDON, AUBREE L, THOMAS, PAUL G. · 2019 to 2025
$43.7M
Longitudinal SARS-CoV-2 mRNA vaccine-induced mucosal, serological, and cellular immunity in children and human milkR01AI173194 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Pia S Pannaraj · 2022 to 2026
$4.0M
NIAID NIH HHS 75N93021C00016NIAID NIH HHS R01 AI173194NIAID NIH HHS U01 AI144616
6 · The paper itself

Abstract

backgroundSevere acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants demonstrate predilection for different regions of the respiratory tract. While saliva-based reverse transcription-polymerase chain reaction (RT-PCR) testing is a convenient, cost-effective alternative to nasopharyngeal swabs (NPS), few studies to date have investigated whether saliva sensitivity differs across variants of concern.

methodsSARS-CoV-2 RT-PCR was performed on paired NPS and saliva specimens collected from individuals with acute coronavirus disease 2019 (COVID-19) symptoms or exposure to a COVID-19 household contact. Viral genome sequencing of NPS specimens and Los Angeles County surveillance data were used to determine the variant of infection. Saliva sensitivity was calculated using NPS-positive RT-PCR as the reference standard. Factors contributing to the likelihood of saliva SARS-CoV-2 RT-PCR positivity were evaluated with univariate and multivariable analyses.

resultsBetween June 2020 and December 2022, 548 saliva samples paired with SARS-CoV-2 positive NPS samples were tested by RT-PCR. Overall, saliva sensitivity for SARS-CoV-2 detection was 61.7% (95% CI, 57.6%-65.7%). Sensitivity was highest with Delta infection (79.6%) compared to pre-Delta (58.5%) and Omicron (61.5%) (P = 0.003 and 0.01, respectively). Saliva sensitivity was higher in symptomatic individuals across all variants compared to asymptomatic cases [pre-Delta 80.6% vs 48.3% (P < 0.001), Delta 100% vs 72.5% (P = 0.03), Omicron 78.7% vs 51.2% (P < 0.001)]. Infection with Delta, symptoms, and high NPS viral load were independently associated with 2.99-, 3.45-, and 4.0-fold higher odds of SARS-CoV-2 detection by saliva-based RT-PCR (P = 0.004, <0.001, and <0.001), respectively.

conclusionsAs new variants emerge, evaluating saliva-based testing approaches may be crucial to ensure effective virus detection.

Indexed as

COVID-19COVID-19 Nucleic Acid TestingSalivaSARS-CoV-2Sensitivity and SpecificityAdolescentAdultAgedFemaleHumansMaleMiddle AgedNasopharynxReverse Transcriptase Polymerase Chain ReactionRNA, ViralYoung AdultRNA, Viral

Identifiers

PMID39246012
PMCPMC12001863

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.