Evidence map›Paper›PMID 39550452›Full record

ArticleScientific reports2024

Microfluidic qPCR for detection of 21 common respiratory viruses in children with influenza-like illness.

Thomas J Saville, Hayley Colton, Sheikh Jarju, Edwin P Armitage, Sainabou Drammeh, Simon Tazzyman, Ya Jankey Jagne, Hadijatou J Sallah, Elina Senghore, Cariad M Evans and 2 more

Abstract read
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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Thomas J Saville *Division of Clinical Medicine, School of Medicine and Population Health, The University of Sheffield, Sheffield, UK. t.j.saville@sheffield.ac.uk.
Hayley Colton *Division of Clinical Medicine, School of Medicine and Population Health, The University of Sheffield, Sheffield, UK. h.colton@sheffield.ac.uk.
Sheikh JarjuVaccines and Immunity Theme, Medical Research Council Unit The Gambia at the London, School of Hygiene and Tropical Medicine, PO Box 273, Banjul, The Gambia.
Edwin P ArmitageVaccines and Immunity Theme, Medical Research Council Unit The Gambia at the London, School of Hygiene and Tropical Medicine, PO Box 273, Banjul, The Gambia.
Sainabou DrammehVaccines and Immunity Theme, Medical Research Council Unit The Gambia at the London, School of Hygiene and Tropical Medicine, PO Box 273, Banjul, The Gambia.
Simon TazzymanDepartment of Virology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Ya Jankey JagneVaccines and Immunity Theme, Medical Research Council Unit The Gambia at the London, School of Hygiene and Tropical Medicine, PO Box 273, Banjul, The Gambia.
Hadijatou J SallahVaccines and Immunity Theme, Medical Research Council Unit The Gambia at the London, School of Hygiene and Tropical Medicine, PO Box 273, Banjul, The Gambia.
Elina SenghoreVaccines and Immunity Theme, Medical Research Council Unit The Gambia at the London, School of Hygiene and Tropical Medicine, PO Box 273, Banjul, The Gambia.
Cariad M EvansDivision of Clinical Medicine, School of Medicine and Population Health, The University of Sheffield, Sheffield, UK.
Thomas C DartonDivision of Clinical Medicine, School of Medicine and Population Health, The University of Sheffield, Sheffield, UK.
Thushan I de SilvaDivision of Clinical Medicine, School of Medicine and Population Health, The University of Sheffield, Sheffield, UK.

Funding

National Institute for Health and Care Research NIHR 200636Wellcome TrustWellcome Trust 110058/Z/15/Z
6 · The paper itself

Abstract

Multiple respiratory viruses lead to high morbidity and mortality, yet global surveillance platforms focus primarily on seasonal influenza viruses. The COVID-19 pandemic and new RSV vaccines highlight the importance of a broader approach. Upper respiratory tract swabs from children aged 24-59 months presenting with influenza-like illness in The Gambia were collected during follow-up of a live-attenuated influenza vaccine randomised controlled trial in 2017-18. A microfluidic quantitative polymerase chain reaction (qPCR) assay was established and used to detect 21 respiratory viruses. 76.6% of samples had one or more viruses detected (n = 121/158). The viruses detected most frequently were rhinovirus (n = 37/158, 23.4%) and adenovirus (n = 34/158, 21.5%), followed by parainfluenza virus 3, influenza B and human metapneumovirus B. A third of positive samples had multiple viruses detected (two n = 31/121, 25.6%; three n = 9/121, 7.4%). Our data demonstrates how microfluidic qPCR is a useful tool for high-throughput, comprehensive detection of multiple respiratory viruses in surveillance platforms. Rapidly changing epidemiology exemplifies the need for new, broader approaches to virus surveillance in low-resource settings to respond to future epidemics and to guide the need for and use of new prevention and therapeutic measures.

Indexed as

Influenza, HumanReal-Time Polymerase Chain ReactionRespiratory Tract InfectionsRhinovirusAdenoviridaeChild, PreschoolFemaleHumansInfantInfluenza B virusMaleMicrofluidicsParainfluenza Virus 3, HumanVirusesInfluenza-like illnessMicrofluidicsPolymerase chain reactionRespiratory virusSurveillance

Identifiers

PMID39550452
PMCPMC11569225

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.