Evidence map›Paper›PMID 36836661›Full record

ArticleLife (Basel, Switzerland)2023

Detection of Circulating SARS-CoV-2 Variants of Concern (VOCs) Using a Multiallelic Spectral Genotyping Assay.

Andreas C Chrysostomou, Antonia Aristokleous, Johana Hezka Rodosthenous, Christina Christodoulou, Georgia Stathi, Leondios G Kostrikis

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Virology Applications to the COVID-19 Pandemic.Life (Basel, Switzerland) · 2025
    Article
  3. Article
  4. 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

6 authors.

Andreas C ChrysostomouDepartment of Biological Sciences, University of Cyprus, Aglantzia, 2109 Nicosia, Cyprus.ORCID 0000-0002-5796-1588
Antonia AristokleousDepartment of Biological Sciences, University of Cyprus, Aglantzia, 2109 Nicosia, Cyprus.
Johana Hezka RodosthenousDepartment of Biological Sciences, University of Cyprus, Aglantzia, 2109 Nicosia, Cyprus.
Christina ChristodoulouDepartment of Biological Sciences, University of Cyprus, Aglantzia, 2109 Nicosia, Cyprus.
Georgia StathiDepartment of Biological Sciences, University of Cyprus, Aglantzia, 2109 Nicosia, Cyprus.
Leondios G KostrikisDepartment of Biological Sciences, University of Cyprus, Aglantzia, 2109 Nicosia, Cyprus.ORCID 0000-0002-5340-7109

Funding

This work was co-funded by the Ministry of Health of the Republic of Cyprus, the University of Cyprus and the Cyprus Academy of Sciences, Letters, and Arts through research funds awarded to Professor Leondios G. Kostrikis Ministry of Health of the Republic of Cyprus, the University of Cyprus and the Cyprus Academy of Sciences, Letters, and Arts through research funds
6 · The paper itself

Abstract

Throughout the coronavirus disease 2019 (COVID-19) pandemic, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has continuously evolved, resulting in new variants, some of which possess increased infectivity, immune evasion, and virulence. Such variants have been denoted by the World Health Organization as variants of concern (VOC) because they have resulted in an increased number of cases, posing a strong risk to public health. Thus far, five VOCs have been designated, Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Delta (B.1.617.2), and Omicron (B.1.1.529), including their sublineages. Next-generation sequencing (NGS) can produce a significant amount of information facilitating the study of variants; however, NGS is time-consuming and costly and not efficient during outbreaks, when rapid identification of VOCs is urgently needed. In such periods, there is a need for fast and accurate methods, such as real-time reverse transcription PCR in combination with probes, which can be used for monitoring and screening of the population for these variants. Thus, we developed a molecular beacon-based real-time RT-PCR assay according to the principles of spectral genotyping. This assay employs five molecular beacons that target ORF1a:ΔS3675/G3676/F3677, S:ΔH69/V70, S:ΔE156/F157, S:ΔΝ211, S:ins214EPE, and S:ΔL242/A243/L244, deletions and an insertion found in SARS-CoV-2 VOCs. This assay targets deletions/insertions because they inherently provide higher discrimination capacity. Here, the design process of the molecular beacon-based real-time RT-PCR assay for detection and discrimination of SARS-CoV-2 is presented, and experimental testing using SARS-CoV-2 VOC samples from reference strains (cultured virus) and clinical patient samples (nasopharyngeal samples), which have been previously classified using NGS, were evaluated. Based on the results, it was shown that all molecular beacons can be used under the same real-time RT-PCR conditions, consequently improving the time and cost efficiency of the assay. Furthermore, this assay was able to confirm the genotype of each of the tested samples from various VOCs, thereby constituting an accurate and reliable method for VOC detection and discrimination. Overall, this assay is a valuable tool that can be used for screening and monitoring the population for VOCs or other emerging variants, contributing to limiting their spread and protecting public health.

Indexed as

COVID-19molecular beaconsSARS-CoV-2variants of concern

Identifiers

PMID36836661
PMCPMC9960118

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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.