Evidence map›Paper›PMID 35640400›Full record

ArticleJournal of clinical virology : the official publication of the Pan American Society for Clinical Virology2022

A qualitative RT-PCR assay for the specific identification of the SARS-CoV-2 B.1.1.529 (Omicron) Variant of Concern.

Philippe Corbisier, Mauro Petrillo, Antonio Marchini, Maddalena Querci, Gerhard Buttinger, Meriem Bekliz, Katja Spiess, Charlotta Polacek, Anders Fomsgaard, Guy Van den Eede

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Novel (d)PCR assays for influenza A(H5Nx) viruses clade 2.3.4.4b surveillance.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2025
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  10. A qualitative RT-PCR assay for the specific identification of the SARS-CoV-2 B.1.1.529 (Omicron) Variant of Concern.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2022
    Article
  11. 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

10 authors at 4 institutions in 4 countries.

Philippe CorbisierEuropean Commission, Joint Research Centre (JRC), Geel 2400, Belgium. Electronic address: philippe.corbisier@ec.europa.eu.
Mauro PetrilloSeidor Italy SRL, Milano, Italy.
Antonio MarchiniEuropean Commission, Joint Research Centre (JRC), Geel 2400, Belgium.
Maddalena QuerciEuropean Commission, Joint Research Centre (JRC), Ispra, Italy.
Gerhard ButtingerEuropean Commission, Joint Research Centre (JRC), Geel 2400, Belgium.
Meriem BeklizGeneva Centre for Emerging Viral Diseases, Department of Microbiology and Molecular Medicine, University of Geneva, University Hospital Geneva (HUG), Switzerland.
Katja SpiessVirus Research & Development lab, Department of Virus & Microbiologic Special Diagnostics, Statens Serum Institut, Denmark.
Charlotta PolacekVirus Research & Development lab, Department of Virus & Microbiologic Special Diagnostics, Statens Serum Institut, Denmark.
Anders FomsgaardVirus Research & Development lab, Department of Virus & Microbiologic Special Diagnostics, Statens Serum Institut, Denmark.
Guy Van den EedeEuropean Commission, Joint Research Centre (JRC), Geel 2400, Belgium.
European Commission · BEStatens Serum Institut · DKJoint Research Centre · ITUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe aim of this study was to develop a RT-PCR assay for the specific detection of the SARS-CoV-2 Omicron Variant of Concern (VOC) as a rapid alternative to sequencing.

methodsA RT-PCR was designed in silico and then validated using characterised clinical samples containing Omicron (both BA.1 and BA.2 lineages) and the Omicron synthetic RNA genome. As negative controls, SARS-CoV-2 positive clinical samples collected in May 2020, and synthetic RNA genomes of the isolate Wuhan Hu-1 and of the Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Kappa (B.1.617.1), Iota (B.1.526), Epsilon (B.1.429) and Delta (B.1.617.2) SARS-CoV-2 VOC were used.

resultsExperiments performed using as templates the synthetic RNA genomes demonstrate the high specificity of the PCR-method for the SARS-CoV-2 Omicron. Despite the synthetic RNAs were used at high copy numbers, specific signal was mainly detected with the Omicron synthetic genome. Only a non-specific late signal was detected using the Alpha variant genome, but these results were considered negligible as Alpha VOC has been replaced by the Delta and it is not circulating anymore in the world. Using our method, we confirmed the presence of Omicron on clinical samples containing this variant but not of other SARS-CoV-2 lineages. The method is highly sensitive and can detect up to 1 cp of the Omicron virus per µl.

conclusionsThe method presented here, in combination with other methods in use for detection of SARS-CoV-2, can be used for an early identification of Omicron.

Indexed as

COVID-19SARS-CoV-2HumansReverse Transcriptase Polymerase Chain ReactionRNA, ViralSensitivity and SpecificityRNA, ViralB.1.1.529OmicronRT-PCRSARS-CoV-2Specific identification

Identifiers

PMID35640400
PMCPMC9126828
OpenAlexW4281561136

What OpenQuestion holds

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LicenceCC BY
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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.