Evidence map›Paper›PMID 39109863›Full record

ArticlemSphere2024

Comprehensive contact tracing during an outbreak of alpha-variant SARS-CoV-2 in a rural community reveals less viral genomic diversity and higher household secondary attack rates than expected.

Audun Sivertsen, Nicolay Mortensen, Unni Solem, Eivind Valen, Marie Francoise Bullita, Knut-Arne Wensaas, Sverre Litleskare, Guri Rørtveit, Harleen M S Grewal, Elling Ulvestad

Abstract read
In one paragraph

Article in mSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Audun SivertsenDepartment of Microbiology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-4283-6397
Nicolay MortensenDepartment of Microbiology, Haukeland University Hospital, Bergen, Norway.
Unni SolemUlvik municipality, Ulvik, Norway.
Eivind ValenComputational Biology Unit, Department of Informatics, University of Bergen, Bergen, Norway.
Marie Francoise BullitaUlvik municipality, Ulvik, Norway.
Knut-Arne WensaasNORCE Norwegian Research Centre, Research Unit for General Practice, Bergen, Norway.
Sverre LitleskareNORCE Norwegian Research Centre, Research Unit for General Practice, Bergen, Norway.
Guri RørtveitDepartment of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
Harleen M S GrewalDepartment of Microbiology, Haukeland University Hospital, Bergen, Norway.
Elling UlvestadDepartment of Microbiology, Haukeland University Hospital, Bergen, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sequencing of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genomes throughout the COVID-19 pandemic has generated a wealth of data on viral evolution across populations, but only a few studies have so far explored SARS-CoV-2 evolution across large connected transmission networks. Here, we couple data from SARS-CoV-2 sequencing with contact tracing data from an outbreak with a single origin in a rural Norwegian community where samples from all exposed persons were collected prospectively. A total of 134 nasopharyngeal samples were positive by PCR. Among the 121 retrievable genomes, 81 were identical to the genome of the introductor, thus demonstrating that genomics beyond clustering genotypically similar viral genomes to confirm relatedness offers limited additional value to manual contact tracing. In the cases where mutations were discovered, five small genetic clusters were identified. We observed a household secondary attack rate of 77%, with 92% of household members infected among households with secondary transmission, suggesting that SARS-CoV-2 introduction into large families is likely to affect all household members. IMPORTANCE: In outbreak investigations, obtaining a full overview of infected individuals within a population is seldom achieved. We here present an example where a single introduction of B1.1.7 SARS-CoV-2 within a rural community allowed for tracing of the virus from an introductor via dissemination through larger gatherings into households. The outbreak occurred before widespread vaccination, allowing for a "natural" outbreak development with community lockdown. We show through sequencing that the virus can infect up to five consecutive persons without gaining mutations, thereby showing that contact tracing seems more important than sequencing for local outbreak investigations in settings with few alternative introductory transmission pathways. We also show how larger households where a child introduced transmission appeared more likely to promote further spread of the virus compared to households with an adult as the primary introductor.

Indexed as

Contact TracingCOVID-19Disease OutbreaksFamily CharacteristicsGenome, ViralRural PopulationSARS-CoV-2AdolescentAdultAgedAged, 80 and overChildChild, PreschoolFemaleGenetic VariationHumanscoronavirusgenome analysismolecular epidemiology

Identifiers

PMID39109863
PMCPMC11351100

What OpenQuestion holds

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LicenceCC BY
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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.