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Airway response to respiratory syncytial virus has incidental antibacterial effects.

Sande, CJ; Njunge, JM; Mwongeli Ngoi, J; Mutunga, MN; Chege, T; Gicheru, ET; Gardiner, EM; Gwela, A; Green, CA; Drysdale, SB; et al. Sande, CJ; Njunge, JM; Mwongeli Ngoi, J; Mutunga, MN; Chege, T; Gicheru, ET; Gardiner, EM; Gwela, A; Green, CA; Drysdale, SB; Berkley, JA; Nokes, DJ; Pollard, AJ (2019) Airway response to respiratory syncytial virus has incidental antibacterial effects. Nat Commun, 10 (1). p. 2218. ISSN 2041-1723 https://doi.org/10.1038/s41467-019-10222-z
SGUL Authors: Drysdale, Simon Bruce

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Abstract

RSV infection is typically associated with secondary bacterial infection. We hypothesise that the local airway immune response to RSV has incidental antibacterial effects. Using coordinated proteomics and metagenomics analysis we simultaneously analysed the microbiota and proteomes of the upper airway and determined direct antibacterial activity in airway secretions of RSV-infected children. Here, we report that the airway abundance of Streptococcus was higher in samples collected at the time of RSV infection compared with samples collected one month later. RSV infection is associated with neutrophil influx into the airway and degranulation and is marked by overexpression of proteins with known antibacterial activity including BPI, EPX, MPO and AZU1. Airway secretions of children infected with RSV, have significantly greater antibacterial activity compared to RSV-negative controls. This RSV-associated, neutrophil-mediated antibacterial response in the airway appears to act as a regulatory mechanism that modulates bacterial growth in the airways of RSV-infected children.

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly fromthe copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. © The Author(s) 2019 Correction available at https://doi.org/10.1038/s41467-019-11222-9
Keywords: Bacterial Infections, Cell Degranulation, Child, Preschool, Humans, Infant, Infant, Newborn, Kenya, Metagenomics, Microbiota, Neutrophils, Proteomics, Respiratory Mucosa, Respiratory Syncytial Virus Infections, Respiratory Syncytial Virus, Human, Streptococcus, Respiratory Mucosa, Neutrophils, Humans, Streptococcus, Respiratory Syncytial Virus, Human, Bacterial Infections, Respiratory Syncytial Virus Infections, Proteomics, Cell Degranulation, Child, Preschool, Infant, Infant, Newborn, Kenya, Metagenomics, Microbiota, MD Multidisciplinary
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
17 May 2019Published
26 April 2019Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
WT105882MAWellcome Trusthttp://dx.doi.org/10.13039/100004440
PubMed ID: 31101811
Web of Science ID: WOS:000468174600018
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/112160
Publisher's version: https://doi.org/10.1038/s41467-019-10222-z

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