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Airway response to respiratory syncytial virus has incidental antibacterial effects
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 airw...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525170/ https://www.ncbi.nlm.nih.gov/pubmed/31101811 http://dx.doi.org/10.1038/s41467-019-10222-z |
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author | Sande, Charles J. Njunge, James M. Mwongeli Ngoi, Joyce Mutunga, Martin N. Chege, Timothy Gicheru, Elijah T. Gardiner, Elizabeth M. Gwela, Agnes Green, Christopher A. Drysdale, Simon B. Berkley, James A. Nokes, D. James Pollard, Andrew J. |
author_facet | Sande, Charles J. Njunge, James M. Mwongeli Ngoi, Joyce Mutunga, Martin N. Chege, Timothy Gicheru, Elijah T. Gardiner, Elizabeth M. Gwela, Agnes Green, Christopher A. Drysdale, Simon B. Berkley, James A. Nokes, D. James Pollard, Andrew J. |
author_sort | Sande, Charles J. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6525170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65251702019-05-20 Airway response to respiratory syncytial virus has incidental antibacterial effects Sande, Charles J. Njunge, James M. Mwongeli Ngoi, Joyce Mutunga, Martin N. Chege, Timothy Gicheru, Elijah T. Gardiner, Elizabeth M. Gwela, Agnes Green, Christopher A. Drysdale, Simon B. Berkley, James A. Nokes, D. James Pollard, Andrew J. Nat Commun Article 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. Nature Publishing Group UK 2019-05-17 /pmc/articles/PMC6525170/ /pubmed/31101811 http://dx.doi.org/10.1038/s41467-019-10222-z Text en © The Author(s) 2019 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 from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sande, Charles J. Njunge, James M. Mwongeli Ngoi, Joyce Mutunga, Martin N. Chege, Timothy Gicheru, Elijah T. Gardiner, Elizabeth M. Gwela, Agnes Green, Christopher A. Drysdale, Simon B. Berkley, James A. Nokes, D. James Pollard, Andrew J. Airway response to respiratory syncytial virus has incidental antibacterial effects |
title | Airway response to respiratory syncytial virus has incidental antibacterial effects |
title_full | Airway response to respiratory syncytial virus has incidental antibacterial effects |
title_fullStr | Airway response to respiratory syncytial virus has incidental antibacterial effects |
title_full_unstemmed | Airway response to respiratory syncytial virus has incidental antibacterial effects |
title_short | Airway response to respiratory syncytial virus has incidental antibacterial effects |
title_sort | airway response to respiratory syncytial virus has incidental antibacterial effects |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525170/ https://www.ncbi.nlm.nih.gov/pubmed/31101811 http://dx.doi.org/10.1038/s41467-019-10222-z |
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