Evidence map›Paper›PMID 34538333›Full record

Trial reportAnalytica chimica acta2021

An ultrafast SARS-CoV-2 virus enrichment and extraction method compatible with multiple modalities for RNA detection.

Leah M Dignan, Rachelle Turiello, Tiffany R Layne, Killian C O'Connell, Jeff Hickey, Jeff Chapman, Melinda D Poulter, James P Landers

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Analytica chimica acta, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
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

8 authors.

Leah M DignanDepartments of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
Rachelle TurielloDepartments of Chemistry, University of Virginia, Charlottesville, VA 22904, USA. Electronic address: rat3a@virginia.edu.
Tiffany R LayneDepartments of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
Killian C O'ConnellDepartments of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
Jeff HickeyMicroGEM International PLC., Charlottesville, VA 22904, USA.
Jeff ChapmanMicroGEM International PLC., Charlottesville, VA 22904, USA.
Melinda D PoulterDepartments of Pathology, University of Virginia, Charlottesville, VA 22904, USA.
James P LandersDepartments of Chemistry, University of Virginia, Charlottesville, VA 22904, USA; MicroGEM International PLC., Charlottesville, VA 22904, USA; Departments of Pathology, University of Virginia, Charlottesville, VA 22904, USA; Departments of Clinical Microbiology, University of Virginia, Charlottesville, VA 22904, USA; Departments of Mechanical and Aerospace Engineering, University of Virginia, Charlottesville, VA 22904, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a zoonotic RNA virus characterized by high transmission rates and pathogenicity worldwide. Continued control of the COVID-19 pandemic requires the diversification of rapid, easy to use, sensitive, and portable methods for SARS-CoV-2 sample preparation and analysis. Here, we propose a method for SARS-CoV-2 viral enrichment and enzymatic extraction of RNA from clinically relevant matrices in under 10 min. This technique utilizes affinity-capture hydrogel particles to concentrate SARS-CoV-2 from solution, and leverages existing PDQeX technology for RNA isolation. Characterization of our method is accomplished with reverse transcription real-time polymerase chain reaction (RT-PCR) for relative, comparative RNA detection. In a double-blind study analyzing viral transport media (VTM) obtained from clinical nasopharyngeal swabs, our sample preparation method demonstrated both comparable results to a routinely used commercial extraction kit and 100% concordance with laboratory diagnoses. Compatibility of eluates with alternative forms of analysis was confirmed using microfluidic RT-PCR (μRT-PCR), recombinase polymerase amplification (RPA), and loop-mediated isothermal amplification (LAMP). The alternative methods explored here conveyed successful amplification from all RNA eluates originating from positive clinical samples. Finally, this method demonstrated high performance within a saliva matrix across a broad range of viral titers and dilutions up to 90% saliva matrix, and sets the stage for miniaturization to the microscale.

Indexed as

COVID-19PandemicsCOVID-19 TestingHumansMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesRNA, ViralSARS-CoV-2RNA, ViralAffinity nanoparticlesEnzymatic extractionLoop-mediated amplification (LAMP)Polymerase chain reaction (PCR)Recombinase polymerase amplification (RPA)Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2)

Identifiers

PMID34538333
PMCPMC8277111

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.