Evidence map›Paper›PMID 39468221›Full record

ArticleScientific reports2024

Recombinant SARS-CoV-2 Delta/Omicron BA.5 emerging in an immunocompromised long-term infected COVID-19 patient.

Ignacio Garcia, Jon Bråte, Even Fossum, Andreas Rohringer, Line V Moen, Olav Hungnes, Olav Fjære, Kyriakos Zaragkoulias, Karoline Bragstad

Abstract readCase Reports
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

9 authors.

Ignacio GarciaDepartment of Bacteriology, Norwegian Institute of Public Health, Oslo, Norway.
Jon BråteDepartment of Virology, Norwegian Institute of Public Health, Oslo, Norway.
Even FossumDepartment of Virology, Norwegian Institute of Public Health, Oslo, Norway.
Andreas RohringerDepartment of Virology, Norwegian Institute of Public Health, Oslo, Norway.
Line V MoenDepartment of Virology, Norwegian Institute of Public Health, Oslo, Norway.
Olav HungnesDepartment of Virology, Norwegian Institute of Public Health, Oslo, Norway.
Olav FjæreSection for Infectious Diseases, Department of Internal Medicine, Levanger Hospital, Nord-Trøndelag Hospital Trust, Levanger, Norway.
Kyriakos ZaragkouliasSection for Medical Microbiology, Department of Laboratory Medicine, Levanger Hospital, Nord-Trøndelag Hospital Trust, Levanger, Norway.
Karoline BragstadDepartment of Virology, Norwegian Institute of Public Health, Oslo, Norway. iggl@fhi.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of the SARS-CoV-2 virus led to a global pandemic, prompting extensive research efforts to understand its molecular biology, transmission dynamics, and pathogenesis. Recombination events have been increasingly recognized as significant contributor to the virus's diversity and evolution, potentially leading to the emergence of novel strains with altered biological properties. Indeed, recombinant lineages such as the XBB variant and its descendants have subsequently dominated globally. Therefore, continued surveillance and monitoring of viral genome diversity are crucial to identify and understand the emergence and spread of novel strains. Through routine genomic surveillance of SARS-CoV-2 cases in Norway, we discovered a SARS-CoV-2 recombination event in a long-term infected immunocompromised COVID-19 (coronavirus disease) patient. A deeper investigation showed several recombination events between two distinct lineages of the virus, namely AY.98.1 and BA.5, that resulted in a single novel recombinant viral strain with a unique genetic signature. Our data is consistent with the presence of several concomitant recombinants in the patient, suggesting that these events occur frequently in vivo. This study underscores the importance of continued tracking of viral diversity and the potential impact of recombination events on the evolution of the SARS-CoV-2 virus.

Indexed as

COVID-19Genome, ViralImmunocompromised HostRecombination, GeneticSARS-CoV-2HumansNorwayPhylogenyDeltaImmunocompromisedIn-patient recombination eventOmicronRecombinantSARS-CoV-2

Identifiers

PMID39468221
PMCPMC11519929

What OpenQuestion holds

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Registered trials

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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.