Evidence map›Paper›PMID 35273232›Full record

ArticleScientific reports2022

Single-tube collection and nucleic acid analysis of clinical samples for SARS-CoV-2 saliva testing.

Kyle H Cole, Alexis Bouin, Caila Ruiz, Bert L Semler, Matthew A Inlay, Andrej Lupták

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Review
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

6 authors.

Kyle H ColeDepartment of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA, 92697, USA.
Alexis BouinDepartment of Microbiology and Molecular Genetics, University of California, Irvine, Irvine, CA, 92697, USA.
Caila RuizDepartment of Pharmaceutical Sciences, University of California, Irvine, Irvine, CA, 92697, USA.
Bert L SemlerDepartment of Microbiology and Molecular Genetics, University of California, Irvine, Irvine, CA, 92697, USA.
Matthew A InlayDepartment of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA, 92697, USA.
Andrej LuptákDepartment of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA, 92697, USA. aluptak@uci.edu.

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
Synthesis of enterovirus positive-strand RNAs: discovery of viral and host determinants of RNP complex formationR21AI145003 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI PASCAL, STEVEN, SEMLER, BERT L · 2020 to 2021
$433k
Division of Chemical, Bioengineering, Environmental, and Transport Systems 1804220National Institute of Allergy and Infectious Diseases AI145003NCI NIH HHS P30 CA062203NIAID NIH HHS R21 AI145003University of California, Irvine COVID-19 Basic, Translational and Clinical Research Funding OpportunityUniversity of California, Irvine ZotFunder "Simple and Rapid COVID-19 Diagnostic Test"
6 · The paper itself

Abstract

The SARS-CoV-2 pandemic has brought to light the need for expedient diagnostic testing. Cost and availability of large-scale testing capacity has led to a lag in turnaround time and hindered contact tracing efforts, resulting in a further spread of SARS-CoV-2. To increase the speed and frequency of testing, we developed a cost-effective single-tube approach for collection, denaturation, and analysis of clinical samples. The approach utilizes 1 µL microbiological inoculation loops to collect saliva, sodium dodecyl sulfate (SDS) to inactivate and release viral genomic RNA, and a diagnostic reaction mix containing polysorbate 80 (Tween 80). In the same tube, the SDS-denatured clinical samples are introduced to the mixtures containing all components for nucleic acids detection and Tween 80 micelles to absorb the SDS and allow enzymatic reactions to proceed, obviating the need for further handling of the samples. The samples can be collected by the tested individuals, further decreasing the need for trained personnel to administer the test. We validated this single-tube sample-to-assay method with reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) and reverse transcription loop-mediated isothermal amplification (RT-LAMP) and discovered little-to-no difference between Tween- and SDS-containing reaction mixtures, compared to control reactions. This approach reduces the logistical burden of traditional large-scale testing and provides a method of deployable point-of-care diagnostics to increase testing frequency.

Indexed as

COVID-19 Nucleic Acid TestingHumansMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesReal-Time Polymerase Chain ReactionSalivaSARS-CoV-2Specimen Handling

Identifiers

PMID35273232
PMCPMC8913774

What OpenQuestion holds

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Registered trials

None linked

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.