Evidence map›Paper›PMID 39014481›Full record

ArticleGenome medicine2024

SARS-CoV-2 population dynamics in immunocompetent individuals in a closed transmission chain shows genomic diversity over the course of infection.

Hannah Goldswain, Rebekah Penrice-Randal, I'ah Donovan-Banfield, Craig W Duffy, Xiaofeng Dong, Nadine Randle, Yan Ryan, Aleksandra M Rzeszutek, Jack Pilgrim, Emma Keyser and 9 more

Abstract read
In one paragraph

Article in Genome medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 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

19 authors.

Hannah GoldswainInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
Rebekah Penrice-RandalInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
I'ah Donovan-BanfieldInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
Craig W DuffyInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
Xiaofeng DongInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
Nadine RandleInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
Yan RyanInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
Aleksandra M RzeszutekCentre for Genomic Research, University of Liverpool, Liverpool, L69 3BX, UK.
Jack PilgrimCentre for Genomic Research, University of Liverpool, Liverpool, L69 3BX, UK.
Emma KeyserDefence Science Technology Laboratory, Porton Down, Salisbury, SP4 0JQ, UK.
Simon A WellerDefence Science Technology Laboratory, Porton Down, Salisbury, SP4 0JQ, UK.
Emma J HutleyCentre for Defence Pathology, Royal Centre for Defence Medicine, OCT Centre, Birmingham, B15 2WB, UK.
Catherine HartleyInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
Tessa PrinceInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
Alistair C DarbyInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK.
Niall Aye MaungBritish Army, Hunter House, St Omer Barracks, Aldershot, Hampshire, GU11 2BG, UK.
Henry NwumeDefence Science Technology Laboratory, Porton Down, Salisbury, SP4 0JQ, UK.
Julian A HiscoxInstitute for Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, L3 5RF, UK. julian.hiscox@liverpool.ac.uk.ORCID 0000-0002-6582-0275
Stevan R EmmettDefence Science Technology Laboratory, Porton Down, Salisbury, SP4 0JQ, UK. sremmett@mail.dstl.gov.uk.

Funding

Medical Research Council MR/W005611/1Medical Research Council MR/Y004205/1U.S. Food and Drug Administration 75F40120C00085
6 · The paper itself

Abstract

backgroundSARS-CoV-2 remains rapidly evolving, and many biologically important genomic substitutions/indels have characterised novel SARS-CoV-2 lineages, which have emerged during successive global waves of the pandemic. Worldwide genomic sequencing has been able to monitor these waves, track transmission clusters, and examine viral evolution in real time to help inform healthcare policy. One school of thought is that an apparent greater than average divergence in an emerging lineage from contemporary variants may require persistent infection, for example in an immunocompromised host. Due to the nature of the COVID-19 pandemic and sampling, there were few studies that examined the evolutionary trajectory of SARS-CoV-2 in healthy individuals.

methodsWe investigated viral evolutionary trends and participant symptomatology within a cluster of 16 SARS-CoV-2 infected, immunocompetent individuals with no co-morbidities in a closed transmission chain. Longitudinal nasopharyngeal swab sampling allowed characterisation of SARS-CoV-2 intra-host variation over time at both the dominant and minor genomic variant levels through Nimagen-Illumina sequencing.

resultsA change in viral lineage assignment was observed in individual infections; however, there was only one indel and no evidence of recombination over the period of an acute infection. Minor and dominant genomic modifications varied between participants, with some minor genomic modifications increasing in abundance to become the dominant viral sequence during infection.

conclusionsData from this cohort of SARS-CoV-2-infected participants demonstrated that long-term persistent infection in an immunocompromised host was not necessarily a prerequisite for generating a greater than average frequency of amino acid substitutions. Amino acid substitutions at both the dominant and minor genomic sequence level were observed in immunocompetent individuals during infection showing that viral lineage changes can occur generating viral diversity.

Indexed as

COVID-19Genome, ViralSARS-CoV-2AdultAgedEvolution, MolecularFemaleGenetic VariationHumansImmunocompetenceMaleMiddle AgedPhylogenyMinor variantsSARS-CoV-2Transmission clusterViral evolution

Identifiers

PMID39014481
PMCPMC11251137

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.