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The bronchial epithelial cell bacterial microbiome and host response in patients infected with human immunodeficiency virus

BACKGROUND: Chronic Obstructive Pulmonary Disease (COPD) is an important comorbidity in patients living with human immunodeficiency virus (HIV). Previous bacterial microbiome studies have shown increased abundance of specific bacterium, like Tropheryma whipplei, and no overall community differences....

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Autores principales: Sze, Marc A., Xu, Stella, Leung, Janice M., Vucic, Emily A., Shaipanich, Tawimas, Moghadam, Aida, Harris, Marianne, Guillemi, Silvia, Sinha, Sunita, Nislow, Corey, Murphy, Darra, Hague, Cameron, Leipsic, Jonathon, Lam, Stephen, Lam, Wan, Montaner, Julio S., Sin, Don D., Man, S. F. Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103452/
https://www.ncbi.nlm.nih.gov/pubmed/27829448
http://dx.doi.org/10.1186/s12890-016-0303-4
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author Sze, Marc A.
Xu, Stella
Leung, Janice M.
Vucic, Emily A.
Shaipanich, Tawimas
Moghadam, Aida
Harris, Marianne
Guillemi, Silvia
Sinha, Sunita
Nislow, Corey
Murphy, Darra
Hague, Cameron
Leipsic, Jonathon
Lam, Stephen
Lam, Wan
Montaner, Julio S.
Sin, Don D.
Man, S. F. Paul
author_facet Sze, Marc A.
Xu, Stella
Leung, Janice M.
Vucic, Emily A.
Shaipanich, Tawimas
Moghadam, Aida
Harris, Marianne
Guillemi, Silvia
Sinha, Sunita
Nislow, Corey
Murphy, Darra
Hague, Cameron
Leipsic, Jonathon
Lam, Stephen
Lam, Wan
Montaner, Julio S.
Sin, Don D.
Man, S. F. Paul
author_sort Sze, Marc A.
collection PubMed
description BACKGROUND: Chronic Obstructive Pulmonary Disease (COPD) is an important comorbidity in patients living with human immunodeficiency virus (HIV). Previous bacterial microbiome studies have shown increased abundance of specific bacterium, like Tropheryma whipplei, and no overall community differences. However, the host response to the lung microbiome is unknown in patients infected with HIV. METHODS: Two bronchial brush samples were obtained from 21 HIV-infected patients. One brush was used for bacterial microbiome analysis using the Illumina MiSeq(TM) platform, while the other was used to evaluate gene expression patterns of the host using the Affymetrix Human Gene ST 2.0 array. Weighted gene co-expression network analysis was used to determine the relationship between the bacterial microbiome and host gene expression response. RESULTS: The Shannon Diversity was inversely related to only one gene expression module (p = 0.02); whereas evenness correlated with five different modules (p ≤ 0.05). After FDR correction only the Firmicutes phylum was significantly correlated with any modules (FDR < 0.05). These modules were enriched for cilia, transcription regulation, and immune response. Specific operational taxonomic units (OTUs), such as OTU4 (Pasteurellaceae), were able to distinguish HIV patients with and without COPD and severe emphysema. CONCLUSION: These data support the hypothesis that the bacterial microbiome in HIV lungs is associated with specific host immune responses. Whether or not these responses are also seen in non-HIV infected individuals needs to be addressed in future studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-016-0303-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-51034522016-11-10 The bronchial epithelial cell bacterial microbiome and host response in patients infected with human immunodeficiency virus Sze, Marc A. Xu, Stella Leung, Janice M. Vucic, Emily A. Shaipanich, Tawimas Moghadam, Aida Harris, Marianne Guillemi, Silvia Sinha, Sunita Nislow, Corey Murphy, Darra Hague, Cameron Leipsic, Jonathon Lam, Stephen Lam, Wan Montaner, Julio S. Sin, Don D. Man, S. F. Paul BMC Pulm Med Research Article BACKGROUND: Chronic Obstructive Pulmonary Disease (COPD) is an important comorbidity in patients living with human immunodeficiency virus (HIV). Previous bacterial microbiome studies have shown increased abundance of specific bacterium, like Tropheryma whipplei, and no overall community differences. However, the host response to the lung microbiome is unknown in patients infected with HIV. METHODS: Two bronchial brush samples were obtained from 21 HIV-infected patients. One brush was used for bacterial microbiome analysis using the Illumina MiSeq(TM) platform, while the other was used to evaluate gene expression patterns of the host using the Affymetrix Human Gene ST 2.0 array. Weighted gene co-expression network analysis was used to determine the relationship between the bacterial microbiome and host gene expression response. RESULTS: The Shannon Diversity was inversely related to only one gene expression module (p = 0.02); whereas evenness correlated with five different modules (p ≤ 0.05). After FDR correction only the Firmicutes phylum was significantly correlated with any modules (FDR < 0.05). These modules were enriched for cilia, transcription regulation, and immune response. Specific operational taxonomic units (OTUs), such as OTU4 (Pasteurellaceae), were able to distinguish HIV patients with and without COPD and severe emphysema. CONCLUSION: These data support the hypothesis that the bacterial microbiome in HIV lungs is associated with specific host immune responses. Whether or not these responses are also seen in non-HIV infected individuals needs to be addressed in future studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-016-0303-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-09 /pmc/articles/PMC5103452/ /pubmed/27829448 http://dx.doi.org/10.1186/s12890-016-0303-4 Text en © The Author(s). 2016 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 Article
Sze, Marc A.
Xu, Stella
Leung, Janice M.
Vucic, Emily A.
Shaipanich, Tawimas
Moghadam, Aida
Harris, Marianne
Guillemi, Silvia
Sinha, Sunita
Nislow, Corey
Murphy, Darra
Hague, Cameron
Leipsic, Jonathon
Lam, Stephen
Lam, Wan
Montaner, Julio S.
Sin, Don D.
Man, S. F. Paul
The bronchial epithelial cell bacterial microbiome and host response in patients infected with human immunodeficiency virus
title The bronchial epithelial cell bacterial microbiome and host response in patients infected with human immunodeficiency virus
title_full The bronchial epithelial cell bacterial microbiome and host response in patients infected with human immunodeficiency virus
title_fullStr The bronchial epithelial cell bacterial microbiome and host response in patients infected with human immunodeficiency virus
title_full_unstemmed The bronchial epithelial cell bacterial microbiome and host response in patients infected with human immunodeficiency virus
title_short The bronchial epithelial cell bacterial microbiome and host response in patients infected with human immunodeficiency virus
title_sort bronchial epithelial cell bacterial microbiome and host response in patients infected with human immunodeficiency virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103452/
https://www.ncbi.nlm.nih.gov/pubmed/27829448
http://dx.doi.org/10.1186/s12890-016-0303-4
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