Cargando…
Altered gut microbiota in infants is associated with respiratory syncytial virus disease severity
BACKGROUND: Respiratory syncytial virus (RSV) is the number one cause of lower respiratory tract infections in infants. There are still no vaccines or specific antiviral therapies against RSV, mainly due to the inadequate understanding of RSV pathogenesis. Recent data suggest a role for gut microbio...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268675/ https://www.ncbi.nlm.nih.gov/pubmed/32487019 http://dx.doi.org/10.1186/s12866-020-01816-5 |
_version_ | 1783541669197512704 |
---|---|
author | Harding, Jeffrey N. Siefker, David Vu, Luan You, Dahui DeVincenzo, John Pierre, JF. Cormier, Stephania A. |
author_facet | Harding, Jeffrey N. Siefker, David Vu, Luan You, Dahui DeVincenzo, John Pierre, JF. Cormier, Stephania A. |
author_sort | Harding, Jeffrey N. |
collection | PubMed |
description | BACKGROUND: Respiratory syncytial virus (RSV) is the number one cause of lower respiratory tract infections in infants. There are still no vaccines or specific antiviral therapies against RSV, mainly due to the inadequate understanding of RSV pathogenesis. Recent data suggest a role for gut microbiota community structure in determining RSV disease severity. Our objective was to determine the gut microbial profile associated with severe RSV patients, which could be used to help identify at-risk patients and develop therapeutically protective microbial assemblages that may stimulate immuno-protection. RESULTS: We enrolled 95 infants from Le Bonheur during the 2014 to 2016 RSV season. Of these, 37 were well-babies and 58 were hospitalized with RSV. Of the RSV infected babies, 53 remained in the pediatric ward (moderate) and 5 were moved to the pediatric intensive care unit at a later date (severe). Stool samples were collected within 72 h of admission; and the composition of gut microbiota was evaluated via 16S sequencing of fecal DNA. There was a significant enrichment in S24_7, Clostridiales, Odoribacteraceae, Lactobacillaceae, and Actinomyces in RSV (moderate and severe) vs. controls. Patients with severe RSV disease had slightly lower alpha diversity (richness and evenness of the bacterial community) of the gut microbiota compared to patients with moderate RSV and healthy controls. Beta diversity (overall microbial composition) was significantly different between all RSV patients (moderate and severe) compared to controls and had significant microbial composition separating all three groups (control, moderate RSV, and severe RSV). CONCLUSIONS: Collectively, these data demonstrate that a unique gut microbial profile is associated with RSV disease and with severe RSV disease with admission to the pediatric intensive care unit. More mechanistic experiments are needed to determine whether the differences observed in gut microbiota are the cause or consequences of severe RSV disease. |
format | Online Article Text |
id | pubmed-7268675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72686752020-06-08 Altered gut microbiota in infants is associated with respiratory syncytial virus disease severity Harding, Jeffrey N. Siefker, David Vu, Luan You, Dahui DeVincenzo, John Pierre, JF. Cormier, Stephania A. BMC Microbiol Research Article BACKGROUND: Respiratory syncytial virus (RSV) is the number one cause of lower respiratory tract infections in infants. There are still no vaccines or specific antiviral therapies against RSV, mainly due to the inadequate understanding of RSV pathogenesis. Recent data suggest a role for gut microbiota community structure in determining RSV disease severity. Our objective was to determine the gut microbial profile associated with severe RSV patients, which could be used to help identify at-risk patients and develop therapeutically protective microbial assemblages that may stimulate immuno-protection. RESULTS: We enrolled 95 infants from Le Bonheur during the 2014 to 2016 RSV season. Of these, 37 were well-babies and 58 were hospitalized with RSV. Of the RSV infected babies, 53 remained in the pediatric ward (moderate) and 5 were moved to the pediatric intensive care unit at a later date (severe). Stool samples were collected within 72 h of admission; and the composition of gut microbiota was evaluated via 16S sequencing of fecal DNA. There was a significant enrichment in S24_7, Clostridiales, Odoribacteraceae, Lactobacillaceae, and Actinomyces in RSV (moderate and severe) vs. controls. Patients with severe RSV disease had slightly lower alpha diversity (richness and evenness of the bacterial community) of the gut microbiota compared to patients with moderate RSV and healthy controls. Beta diversity (overall microbial composition) was significantly different between all RSV patients (moderate and severe) compared to controls and had significant microbial composition separating all three groups (control, moderate RSV, and severe RSV). CONCLUSIONS: Collectively, these data demonstrate that a unique gut microbial profile is associated with RSV disease and with severe RSV disease with admission to the pediatric intensive care unit. More mechanistic experiments are needed to determine whether the differences observed in gut microbiota are the cause or consequences of severe RSV disease. BioMed Central 2020-06-01 /pmc/articles/PMC7268675/ /pubmed/32487019 http://dx.doi.org/10.1186/s12866-020-01816-5 Text en © The Author(s) 2020 Open AccessThis 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 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 in a credit line to the data. |
spellingShingle | Research Article Harding, Jeffrey N. Siefker, David Vu, Luan You, Dahui DeVincenzo, John Pierre, JF. Cormier, Stephania A. Altered gut microbiota in infants is associated with respiratory syncytial virus disease severity |
title | Altered gut microbiota in infants is associated with respiratory syncytial virus disease severity |
title_full | Altered gut microbiota in infants is associated with respiratory syncytial virus disease severity |
title_fullStr | Altered gut microbiota in infants is associated with respiratory syncytial virus disease severity |
title_full_unstemmed | Altered gut microbiota in infants is associated with respiratory syncytial virus disease severity |
title_short | Altered gut microbiota in infants is associated with respiratory syncytial virus disease severity |
title_sort | altered gut microbiota in infants is associated with respiratory syncytial virus disease severity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268675/ https://www.ncbi.nlm.nih.gov/pubmed/32487019 http://dx.doi.org/10.1186/s12866-020-01816-5 |
work_keys_str_mv | AT hardingjeffreyn alteredgutmicrobiotaininfantsisassociatedwithrespiratorysyncytialvirusdiseaseseverity AT siefkerdavid alteredgutmicrobiotaininfantsisassociatedwithrespiratorysyncytialvirusdiseaseseverity AT vuluan alteredgutmicrobiotaininfantsisassociatedwithrespiratorysyncytialvirusdiseaseseverity AT youdahui alteredgutmicrobiotaininfantsisassociatedwithrespiratorysyncytialvirusdiseaseseverity AT devincenzojohn alteredgutmicrobiotaininfantsisassociatedwithrespiratorysyncytialvirusdiseaseseverity AT pierrejf alteredgutmicrobiotaininfantsisassociatedwithrespiratorysyncytialvirusdiseaseseverity AT cormierstephaniaa alteredgutmicrobiotaininfantsisassociatedwithrespiratorysyncytialvirusdiseaseseverity |