Evidence map›Paper›PMID 34960813›Full record

ArticleViruses2021

Prediction of SARS-CoV-2 Variant Lineages Using the S1-Encoding Region Sequence Obtained by PacBio Single-Molecule Real-Time Sequencing.

Sébastien Lhomme, Justine Latour, Nicolas Jeanne, Pauline Trémeaux, Noémie Ranger, Marion Migueres, Gérald Salin, Cécile Donnadieu, Jacques Izopet

Abstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Hepatitis A virus infection.Nature reviews. Disease primers · 2023
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. 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

9 authors.

Sébastien LhommeInfinity, Université Toulouse, CNRS, INSERM, UPS, 31300 Toulouse, France.ORCID 0000-0001-7908-1576
Justine LatourLaboratoire de Virologie, CHU Toulouse, Hôpital Purpan, 31300 Toulouse, France.
Nicolas JeanneLaboratoire de Virologie, CHU Toulouse, Hôpital Purpan, 31300 Toulouse, France.ORCID 0000-0001-7109-3353
Pauline TrémeauxLaboratoire de Virologie, CHU Toulouse, Hôpital Purpan, 31300 Toulouse, France.ORCID 0000-0001-8783-9885
Noémie RangerLaboratoire de Virologie, CHU Toulouse, Hôpital Purpan, 31300 Toulouse, France.ORCID 0000-0003-3566-0706
Marion MigueresInfinity, Université Toulouse, CNRS, INSERM, UPS, 31300 Toulouse, France.ORCID 0000-0001-7791-3201
Gérald SalinINRAE, US 1426, GeT-PlaGe, Genotoul, 31326 Castanet-Tolosan, France.ORCID 0000-0003-3580-1249
Cécile DonnadieuINRAE, US 1426, GeT-PlaGe, Genotoul, 31326 Castanet-Tolosan, France.ORCID 0000-0002-5164-3095
Jacques IzopetInfinity, Université Toulouse, CNRS, INSERM, UPS, 31300 Toulouse, France.ORCID 0000-0002-8462-3234

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is the causal agent of the COVID-19 pandemic that emerged in late 2019. The outbreak of variants with mutations in the region encoding the spike protein S1 sub-unit that can make them more resistant to neutralizing or monoclonal antibodies is the main point of the current monitoring. This study examines the feasibility of predicting the variant lineage and monitoring the appearance of reported mutations by sequencing only the region encoding the S1 domain by Pacific Bioscience Single Molecule Real-Time sequencing (PacBio SMRT). Using the PacBio SMRT system, we successfully sequenced 186 of the 200 samples previously sequenced with the Illumina COVIDSeq (whole genome) system. PacBio SMRT detected mutations in the S1 domain that were missed by the COVIDseq system in 27/186 samples (14.5%), due to amplification failure. These missing positions included mutations that are decisive for lineage assignation, such as G142D (

Indexed as

Sequence Analysis, DNACOVID-19GenotypeHumansMutationProtein Interaction Domains and MotifsSARS-CoV-2Spike Glycoprotein, CoronavirusSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2cladeIllumina sequencinglineagePacBio SMRT sequencingS1 domainSARS-CoV-2

Identifiers

PMID34960813
PMCPMC8707593

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.