Evidence map›Paper›PMID 35760381›Full record

ArticleInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases2022

Rapid and qualitative identification of SARS-CoV-2 mutations associated with variants of concern using a multiplex RT-PCR assay coupled with melting analysis.

Giuseppe Sberna, Lavinia Fabeni, Giulia Berno, Fabrizio Carletti, Eliana Specchiarello, Francesca Colavita, Silvia Meschi, Giulia Matusali, Anna Rosa Garbuglia, Licia Bordi and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

11 authors at 1 institution in 1 country.

Giuseppe SbernaLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Lavinia FabeniLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Giulia BernoLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Fabrizio CarlettiLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Eliana SpecchiarelloLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Francesca ColavitaLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Silvia MeschiLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Giulia MatusaliLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Anna Rosa GarbugliaLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Licia BordiLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy. Electronic address: licia.bordi@inmi.it.
Eleonora LalleLaboratorio di Virologia, Istituto Nazionale per le Malattie Infettive (INMI) "Lazzaro Spallanzani" - IRCCS, Rome, Italy.
Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesConsidering the spread of new genetic variants and their impact on public health, it is important to have assays that are able to rapidly detect SARS-CoV-2 variants.

methodsWe retrospectively examined 118 positive nasopharyngeal swabs, first characterized by the Sanger sequencing, using the Simplexa® SARS-CoV-2 Variants Direct assay, with the aim of evaluating the performance of the assay to detect N501Y, G496S, Q498R, Y505H, E484K, E484Q, E484A, and L452R mutations.

resultsA total of 111/118 nasopharyngeal swabs were in complete agreement with the Sanger sequencing, whereas the remaining seven samples were not amplified due to the low viral load. The evaluation of the ability of the assay to detect the E484Q mutation was performed using a viral isolate of the SARS-CoV-2 Kappa variant, showing concordance in 15/15 samples. Simplexa® SARS-CoV-2 Variant Direct assay was able to detect mutation pattern of Alpha, Beta, Gamma, Delta, and Omicron variants with 100% specificity and 94% sensitivity, whereas 100% sensitivity and specificity for the Kappa variant was observed.

conclusionThe assay can be useful to obtain faster results, contributing to a prompt surveillance of SARS-CoV-2 variants; however, it requires to be confirmed by the Sanger method, especially in the case of pattern of mutations that are different from those expected and also requires updates as new variants emerge.

Indexed as

COVID-19SARS-CoV-2COVID-19 TestingHumansMutationRetrospective StudiesReverse Transcriptase Polymerase Chain ReactionRNA, ViralRNA, ViralMelting analysisRapid identificationRT-PCRSARS-CoV-2Variants of concern

Identifiers

PMID35760381
PMCPMC9233866
OpenAlexW4283519770

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.