Evidence map›Paper›PMID 36333340›Full record

ArticleScientific reports2022

SARS-CoV-2 quasi-species analysis from patients with persistent nasopharyngeal shedding.

Pierre Dudouet, Philippe Colson, Sarah Aherfi, Anthony Levasseur, Mamadou Beye, Jeremy Delerce, Emilie Burel, Philippe Lavrard, Wahiba Bader, Jean-Christophe Lagier and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  5. SARS-CoV-2 mutant spectrum complexity is an epidemiologically evolvable trait.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

13 authors at 4 institutions in 2 countries.

Pierre DudouetIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France. pierre.dudouet@univ-amu.fr.
Philippe ColsonIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Sarah AherfiIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Anthony LevasseurIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Mamadou BeyeIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Jeremy DelerceIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Emilie BurelIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Philippe LavrardIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Wahiba BaderIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Jean-Christophe LagierIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Pierre-Edouard FournierIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Bernard La ScolaIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Didier RaoultIHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Méditerranée Infection Foundation · FRInstitut de Recherche Pour le Développement · BFInstitut de Recherche pour le Développement · FRUnité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At the time of a new and unprecedented viral pandemic, many questions are being asked about the genomic evolution of SARS-CoV-2 and the emergence of different variants, leading to therapeutic and immune evasion and survival of this genetically highly labile RNA virus. The nasopharyngeal persistence of infectious virus beyond 17 days proves its constant interaction with the human immune system and increases the intra-individual mutational possibilities. We performed a prospective high-throughput sequencing study (ARTIC Nanopore) of SARS-CoV-2 from so-called "persistent" patients, comparing them with a non-persistent population, and analyzing the quasi-species present in a single sample at time t. Global intra-individual variability in persistent patients was found to be higher than in controls (mean 5.3%, Standard deviation 0.9 versus 4.6% SD 0.3, respectively, p < 0.001). In the detailed analysis, we found a greater difference between persistent and non-persistent patients with non-severe COVID 19, and between the two groups infected with clade 20A. Furthermore, we found minority N501Y and P681H mutation clouds in all patients, with no significant differences found both groups. The question of the SARS-CoV-2 viral variants' genesis remains to be further investigated, with the need to prevent new viral propagations and their consequences, and quasi-species analysis could be an important key to watch out.

Indexed as

COVID-19SARS-CoV-2HumansProspective StudiesQuasispecies

Identifiers

PMID36333340
PMCPMC9636146
OpenAlexW4308212791

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.