Evidence map›Paper›PMID 38493135›Full record

ArticleNature communications2024

Targeted metagenomics reveals association between severity and pathogen co-detection in infants with respiratory syncytial virus.

Gu-Lung Lin, Simon B Drysdale, Matthew D Snape, Daniel O'Connor, Anthony Brown, George MacIntyre-Cockett, Esther Mellado-Gomez, Mariateresa de Cesare, M Azim Ansari, David Bonsall and 11 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
14.3field-weighted citation impact, top 1% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
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  6. bioRxiv : the preprint server for biology · 2026
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  16. Lower respiratory tract co-infection ofFrontiers in cellular and infection microbiology · 2025
    Article
  17. Article
  18. Salivary polyreactive antibodies andThe European respiratory journal · 2024
    Article
  19. Article
  20. 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

21 authors at 10 institutions in 7 countries.

Gu-Lung LinOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK. gulung.lin.oxford@gmail.com.ORCID http://orcid.org/0000-0002-9950-318X
Simon B DrysdaleOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-6350-6557
Matthew D SnapeOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.
Daniel O'ConnorOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-6902-9886
Anthony BrownPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-6751-3300
George MacIntyre-CockettWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Esther Mellado-GomezWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Mariateresa de CesareWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
M Azim AnsariPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, UK.
David BonsallWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
James E BrayDepartment of Biology, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-3554-4254
Keith A JolleyDepartment of Biology, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-0751-0287
Rory BowdenWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-8596-0366
Jeroen AerssensTranslational Biomarkers, Infectious Diseases Therapeutic Area, Janssen Pharmaceutica NV, Beerse, Belgium.
Louis BontDepartment of Pediatrics, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, Netherlands.ORCID http://orcid.org/0000-0003-3099-4475
Peter J M OpenshawNational Heart and Lung Institute, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-7220-2555
Federico Martinon-TorresTranslational Pediatrics and Infectious Diseases, Pediatrics Department, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0002-9023-581X
Harish NairCentre for Global Health, Usher Institute, Edinburgh Medical School, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-9432-9100
Tanya GolubchikBig Data Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK. tanya.golubchik@sydney.edu.au.ORCID http://orcid.org/0000-0003-2765-9828
Andrew J PollardOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-7361-719X
RESCEU Consortium
Centre for Human Genetics · GBUniversity of Oxford · GBImperial College London · GBJanssen (Belgium) · BEOxford Research Group · GBSt George's, University of London · GBThe University of Sydney · AUUniversidade de Santiago de Compostela · ESUniversity Medical Center Utrecht · NLUniversity of the Witwatersrand · ZA

Funding

Innovative Medicines Initiative (IMI) 116019Royal Society 220171/Z/20/ZWellcome TrustWellcome Trust (Wellcome) 218205/Z/19/ZWellcome Trust (Wellcome) 220171/Z/20/Z
6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) is the leading cause of hospitalisation for respiratory infection in young children. RSV disease severity is known to be age-dependent and highest in young infants, but other correlates of severity, particularly the presence of additional respiratory pathogens, are less well understood. In this study, nasopharyngeal swabs were collected from two cohorts of RSV-positive infants <12 months in Spain, the UK, and the Netherlands during 2017-20. We show, using targeted metagenomic sequencing of >100 pathogens, including all common respiratory viruses and bacteria, from samples collected from 433 infants, that burden of additional viruses is common (111/433, 26%) but only modestly correlates with RSV disease severity. In contrast, there is strong evidence in both cohorts and across age groups that presence of Haemophilus bacteria (194/433, 45%) is associated with higher severity, including much higher rates of hospitalisation (odds ratio 4.25, 95% CI 2.03-9.31). There is no evidence for association between higher severity and other detected bacteria, and no difference in severity between RSV genotypes. Our findings reveal the genomic diversity of additional pathogens during RSV infection in infants, and provide an evidence base for future causal investigations of the impact of co-infection on RSV disease severity.

Indexed as

CoinfectionRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsRespiratory Tract InfectionsChildChild, PreschoolHospitalizationHumansInfant

Identifiers

PMID38493135
PMCPMC10944482
OpenAlexW4392882513

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.