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Nasal commensal Staphylococcus epidermidis enhances interferon-λ-dependent immunity against influenza virus
BACKGROUND: Staphylococcus epidermidis is one of the most abundant colonizers of healthy human mucosa including that in the respiratory tract. As the respiratory microbiome has been linked to host immune responses, this study sought to determine the role of nasal mucosa-associated S. epidermidis in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542144/ https://www.ncbi.nlm.nih.gov/pubmed/31146794 http://dx.doi.org/10.1186/s40168-019-0691-9 |
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author | Kim, Hyun Jik Jo, Ara Jeon, Yung Jin An, Sujin Lee, Kang-Mu Yoon, Sang Sun Choi, Jae Young |
author_facet | Kim, Hyun Jik Jo, Ara Jeon, Yung Jin An, Sujin Lee, Kang-Mu Yoon, Sang Sun Choi, Jae Young |
author_sort | Kim, Hyun Jik |
collection | PubMed |
description | BACKGROUND: Staphylococcus epidermidis is one of the most abundant colonizers of healthy human mucosa including that in the respiratory tract. As the respiratory microbiome has been linked to host immune responses, this study sought to determine the role of nasal mucosa-associated S. epidermidis in innate immune responses against the influenza A virus (IAV). S. epidermidis strains were isolated from nasal mucus samples of healthy individuals. The effects of these mucosa-derived commensal strains on interferon (IFN)-dependent innate immunity and IAV infection dynamics were tested in vitro using normal human nasal epithelial (NHNE) cells and human turbinate mucosa. The effects of S. epidermidis on antiviral immunity were also tested in vivo using an acute IAV infection mouse model. RESULTS: Exposure of NHNE cells to nasal mucosa-derived S. epidermidis increased IFN-λ mRNA and secreted protein levels in the absence of viral stimulation. In the context of IAV infection, NHNE exposure to S. epidermidis prevented an increase in the viral burden, as revealed by IAV PA mRNA abundance, IAV nucleoprotein levels, and viral titers. S. epidermidis also enhanced transcription of IFN-stimulated genes independently of Toll-like receptor 2 and further induced IFN-λ production in IAV-infected cells by promoting phosphorylation of interferon regulatory factor 7. In a murine infection model, S. epidermidis prevented the spread of IAV to the lungs by stimulating IFN-λ innate immunity and suppressing IAV replication in the nasal mucosa. CONCLUSION: The human nasal commensal S. epidermidis mediates front-line antiviral protection against IAV infection through modulation of IFN-λ-dependent innate immune mechanisms in the nasal mucosa, thereby demonstrating the role of host-bacterial commensalism in shaping human antiviral responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0691-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6542144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65421442019-06-04 Nasal commensal Staphylococcus epidermidis enhances interferon-λ-dependent immunity against influenza virus Kim, Hyun Jik Jo, Ara Jeon, Yung Jin An, Sujin Lee, Kang-Mu Yoon, Sang Sun Choi, Jae Young Microbiome Research BACKGROUND: Staphylococcus epidermidis is one of the most abundant colonizers of healthy human mucosa including that in the respiratory tract. As the respiratory microbiome has been linked to host immune responses, this study sought to determine the role of nasal mucosa-associated S. epidermidis in innate immune responses against the influenza A virus (IAV). S. epidermidis strains were isolated from nasal mucus samples of healthy individuals. The effects of these mucosa-derived commensal strains on interferon (IFN)-dependent innate immunity and IAV infection dynamics were tested in vitro using normal human nasal epithelial (NHNE) cells and human turbinate mucosa. The effects of S. epidermidis on antiviral immunity were also tested in vivo using an acute IAV infection mouse model. RESULTS: Exposure of NHNE cells to nasal mucosa-derived S. epidermidis increased IFN-λ mRNA and secreted protein levels in the absence of viral stimulation. In the context of IAV infection, NHNE exposure to S. epidermidis prevented an increase in the viral burden, as revealed by IAV PA mRNA abundance, IAV nucleoprotein levels, and viral titers. S. epidermidis also enhanced transcription of IFN-stimulated genes independently of Toll-like receptor 2 and further induced IFN-λ production in IAV-infected cells by promoting phosphorylation of interferon regulatory factor 7. In a murine infection model, S. epidermidis prevented the spread of IAV to the lungs by stimulating IFN-λ innate immunity and suppressing IAV replication in the nasal mucosa. CONCLUSION: The human nasal commensal S. epidermidis mediates front-line antiviral protection against IAV infection through modulation of IFN-λ-dependent innate immune mechanisms in the nasal mucosa, thereby demonstrating the role of host-bacterial commensalism in shaping human antiviral responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0691-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-30 /pmc/articles/PMC6542144/ /pubmed/31146794 http://dx.doi.org/10.1186/s40168-019-0691-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Kim, Hyun Jik Jo, Ara Jeon, Yung Jin An, Sujin Lee, Kang-Mu Yoon, Sang Sun Choi, Jae Young Nasal commensal Staphylococcus epidermidis enhances interferon-λ-dependent immunity against influenza virus |
title | Nasal commensal Staphylococcus epidermidis enhances interferon-λ-dependent immunity against influenza virus |
title_full | Nasal commensal Staphylococcus epidermidis enhances interferon-λ-dependent immunity against influenza virus |
title_fullStr | Nasal commensal Staphylococcus epidermidis enhances interferon-λ-dependent immunity against influenza virus |
title_full_unstemmed | Nasal commensal Staphylococcus epidermidis enhances interferon-λ-dependent immunity against influenza virus |
title_short | Nasal commensal Staphylococcus epidermidis enhances interferon-λ-dependent immunity against influenza virus |
title_sort | nasal commensal staphylococcus epidermidis enhances interferon-λ-dependent immunity against influenza virus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542144/ https://www.ncbi.nlm.nih.gov/pubmed/31146794 http://dx.doi.org/10.1186/s40168-019-0691-9 |
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