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

Lin, G-L; Drysdale, SB; Snape, MD; O'Connor, D; Brown, A; MacIntyre-Cockett, G; Mellado-Gomez, E; de Cesare, M; Ansari, MA; Bonsall, D; et al. Lin, G-L; Drysdale, SB; Snape, MD; O'Connor, D; Brown, A; MacIntyre-Cockett, G; Mellado-Gomez, E; de Cesare, M; Ansari, MA; Bonsall, D; Bray, JE; Jolley, KA; Bowden, R; Aerssens, J; Bont, L; Openshaw, PJM; Martinon-Torres, F; Nair, H; Golubchik, T; Pollard, AJ; RESCEU Consortium (2024) Targeted metagenomics reveals association between severity and pathogen co-detection in infants with respiratory syncytial virus. Nat Commun, 15 (1). p. 2379. ISSN 2041-1723 https://doi.org/10.1038/s41467-024-46648-3
SGUL Authors: Drysdale, Simon Bruce

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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.

Item Type: Article
Additional Information: Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. © The Author(s) 2024
Keywords: Infant, Child, Humans, Child, Preschool, Respiratory Syncytial Virus, Human, Respiratory Syncytial Virus Infections, Respiratory Tract Infections, Hospitalization, Coinfection, RESCEU Consortium, Humans, Respiratory Syncytial Virus, Human, Respiratory Tract Infections, Respiratory Syncytial Virus Infections, Hospitalization, Child, Child, Preschool, Infant, Coinfection
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Nat Commun
ISSN: 2041-1723
Language: eng
Dates:
DateEvent
16 March 2024Published
23 February 2024Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
116019Innovative Medicines Initiative (IMI)UNSPECIFIED
PI1601569Instituto de Salud Carlos IIIhttp://dx.doi.org/10.13039/501100004587
PI1901090Instituto de Salud Carlos IIIhttp://dx.doi.org/10.13039/501100004587
PI22/00406Instituto de Salud Carlos IIIhttp://dx.doi.org/10.13039/501100004587
GNT2025445National Health and Medical Research Councilhttp://dx.doi.org/10.13039/501100000925
220171/Z/20/ZRoyal Societyhttp://dx.doi.org/10.13039/501100000288
220171/Z/20/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
218205/Z/19/ZWellcome TrustUNSPECIFIED
PubMed ID: 38493135
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116364
Publisher's version: https://doi.org/10.1038/s41467-024-46648-3

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