Evidence map›Paper›PMID 36759003›Full record

ArticleBMJ military health2024

Deployment of whole genome next-generation sequencing of SARS-CoV-2 in a military maritime setting.

Andrew Bosworth, J Robson, B Lawrence, A L Casey, A Fair, S Khanam, C Hudson, M K O'Shea

Abstract read
In one paragraph

Article in BMJ military health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

8 authors.

Andrew BosworthDepartment of Microbiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
J RobsonDepartment of Microbiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
B LawrenceDefence Pathology, Royal Centre for Defence Medicine, Birmingham, UK.
A L CaseyDepartment of Microbiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
A FairMolecular Pathology Diagnostic Service, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
S KhanamDepartment of Microbiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
C HudsonDepartment of Microbiology, Frimley Park Hospital, Camberley, UK.
M K O'SheaInstitute for Immunology and Immunotherapy, University of Birmingham College of Medical and Dental Sciences, Birmingham, UK m.k.oshea@bham.ac.uk.ORCID http://orcid.org/0000-0001-6414-8088

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSARS-CoV-2 can spread rapidly on maritime platforms. Several outbreaks of SARS-CoV-2 have been reported on warships at sea, where transmission is facilitated by living and working in close quarters. Core components of infection control measures such as social distancing, patient isolation and quarantine of exposed persons are extremely difficult to implement. Whole genome sequencing (WGS) of SARS-CoV-2 has facilitated epidemiological investigations of outbreaks, impacting on outbreak management in real time by identifying transmission patterns, clusters of infection and guiding control measures. We suggest such a capability could mitigate against the impact of SARS-CoV-2 in maritime settings.

methodsWe set out to establish SARS-CoV-2 WGS using miniaturised nanopore sequencing technology aboard the Royal Fleet Auxiliary ARGUS while at sea. Objectives included designing a simplified protocol requiring minimal reagents and processing steps, the use of miniaturised equipment compatible for use in limited space, and a streamlined and standalone data analysis capability to allow rapid in situ data acquisition and interpretation.

resultsEleven clinical samples with blinded SARS-CoV-2 status were tested at sea. Following viral RNA extraction and ARTIC sequencing library preparation, reverse transcription and ARTIC PCR-tiling were performed. Samples were subsequently barcoded and sequenced using the Oxford Nanopore MinION Mk1B. An offline version of the MinKNOW software was used followed by CLC Genomics Workbench for downstream analysis for variant identification and phylogenetic tree construction. All samples were correctly classified, and relatedness identified.

conclusionsIt is feasible to establish a small footprint sequencing capability to conduct SARS-CoV-2 WGS in a military maritime environment at sea with limited access to reach-back support. This proof-of-concept study has highlighted the potential of deploying such technology in the future to military environments, both maritime and land-based, to provide meaningful clinical data to aid outbreak investigations.

Indexed as

COVID-19Military PersonnelSARS-CoV-2Whole Genome SequencingGenome, ViralHigh-Throughput Nucleotide SequencingHumansShipsCOVID-19molecular biologymolecular diagnostics

Identifiers

PMID36759003
PMCPMC11672050

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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.