Evidence map›Paper›PMID 37052600›Full record

ArticleMicrobial genomics2023

Novel recombinant SARS-CoV-2 lineage detected through genomic surveillance in Wales, UK.

Nicole Pacchiarini, Michelle Cronin, Clare Sawyer, Catie Williams, Andrew Beazer, Simon Cottrell, Mari Morgan, Vince Saunders, Catherine Moore, Thomas R Connor and 1 more

Open access · goldAbstract read
In one paragraph

Article in Microbial genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 94% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Review
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

11 authors at 2 institutions in 1 country.

Nicole PacchiariniCommunicable Disease Surveillance Centre (CDSC), Public Health Wales, Cardiff, Wales, UK.
Michelle CroninCommunicable Disease Surveillance Centre (CDSC), Public Health Wales, Cardiff, Wales, UK.
Clare SawyerCommunicable Disease Surveillance Centre (CDSC), Public Health Wales, Cardiff, Wales, UK.
Catie WilliamsPathogen Genomics Unit, Public Health Wales, Cardiff, Wales, UK.
Andrew BeazerPathogen Genomics Unit, Public Health Wales, Cardiff, Wales, UK.
Simon CottrellCommunicable Disease Surveillance Centre (CDSC), Public Health Wales, Cardiff, Wales, UK.
Mari MorganCommunicable Disease Surveillance Centre (CDSC), Public Health Wales, Cardiff, Wales, UK.
Vince SaundersCardiff and Vale University Health Board, Cardiff, Wales, UK.
Catherine MooreWales Specialist Virology Centre, Microbiology, Public Health Wales, Cardiff, Wales, UK.
Thomas R ConnorPathogen Genomics Unit, Public Health Wales, Cardiff, Wales, UK.
Christopher WilliamsCommunicable Disease Surveillance Centre (CDSC), Public Health Wales, Cardiff, Wales, UK.
Public Health Wales · GBCardiff and Vale University Health Board · GB

Funding

Medical Research Council MR/T030062/1Medical Research Council MR/V028367/1
6 · The paper itself

Abstract

Recombination, the process whereby a segment of genetic material from one genome is inserted into another, producing a new chimeric genome, is an important evolutionary mechanism frequently observed in coronaviruses. The risks posed by recombination include the shuffling of advantageous mutations that may increase transmissibility, severity or vaccine escape. We present a genomic and epidemiological description of a new recombinant lineage of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), XR, first identified in Wales. The Pathogen Genomics Unit (Public Health Wales, UK) sequences positive SARS-CoV-2 PCR tests using the ARTIC SARS-CoV-2 sequencing protocol. Recombinants were detected using an in-house pipeline and the epidemiological data analysed in R. Nosocomial cases were defined as those with samples taken after >7 days in hospital. Between February and March 2022, we identified 78 samples with highly similar genomes, comprising a BA.1-like 5' end, a BA.2-like 3' end and a BA.2-like spike protein. This signature is consistent with recombination and was defined as XR by Pangolin (PANGO v1.8). A total of 50 % of cases had a sample collected whilst in hospital and the first three cases were immunocompromised patients. The patient median age was 58 years (range: 4-95 years) and most of the patients were fully vaccinated against SARS-CoV-2 (74 % third dose/booster). Three patients died within 28 days of their sample collection date, one of whom had COVID-19 listed amongst ICD10 (International Classification of Diseases 10) coded causes of death. Our integrated system enabled real-time monitoring of recombinant SARS-CoV-2 for early detection, in order to rapidly risk assess and respond. This work highlights the importance of setting-based surveillance of recombinant SARS-CoV-2, as well as the need to monitor immunocompromised populations through repeat testing and sequencing.

Indexed as

COVID-19SARS-CoV-2GenomicsHumansMiddle AgedPolymerase Chain ReactionWalesCOVID-19genomicsrecombinationSARS-CoV-2surveillance

Identifiers

PMID37052600
PMCPMC10210960
OpenAlexW4365442758

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.