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The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation
BACKGROUND: Spaceflight impacts astronauts in many ways but little is known on how spaceflight affects the salivary microbiome and the consequences of these changes on astronaut health, such as viral reactivation. In order to understand this, the salivary microbiome was analyzed with 16S rRNA gene a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171750/ https://www.ncbi.nlm.nih.gov/pubmed/32312311 http://dx.doi.org/10.1186/s40168-020-00830-z |
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author | Urbaniak, Camilla Lorenzi, Hernan Thissen, James Jaing, Crystal Crucian, Brian Sams, Clarence Pierson, Duane Venkateswaran, Kasthuri Mehta, Satish |
author_facet | Urbaniak, Camilla Lorenzi, Hernan Thissen, James Jaing, Crystal Crucian, Brian Sams, Clarence Pierson, Duane Venkateswaran, Kasthuri Mehta, Satish |
author_sort | Urbaniak, Camilla |
collection | PubMed |
description | BACKGROUND: Spaceflight impacts astronauts in many ways but little is known on how spaceflight affects the salivary microbiome and the consequences of these changes on astronaut health, such as viral reactivation. In order to understand this, the salivary microbiome was analyzed with 16S rRNA gene amplicon sequencing, and saliva viral titers were analyzed with quantitative polymerase chain reaction (qPCR) with primers specific for Epstein-Barr virus (EBV), herpes simplex virus (HSV), and varicella zoster virus (VZV) from 10 astronauts pre-flight, in-flight, and post-flight. RESULTS: Streptococcus was the most abundant organism in the saliva, making up 8% of the total organisms detected, and their diversity decreased during spaceflight. Other organisms that had statistically significant changes were Proteobacteria and Fusobacteria which increased during flight and Actinobacteria which decreased during flight. At the genus level, Catonella, Megasphera, and Actinobacillus were absent in more than half of saliva samples collected pre-flight but were then detected during flight. In those subjects that already had these genera pre-flight, their relative abundances increased during flight. Correlation analyses between the microbiome and viral titers revealed a positive correlation with Gracilibacteria, Absconditabacteria, and Abiotrophia and a negative correlation between Oribacterium, Veillonella, and Haemophilus. There was also a significant positive correlation between microbiome richness and EBV viral titers. CONCLUSIONS: This is the first study to look at how the salivary microbiome changes as a result of spaceflight and the search for bacterial biomarkers for viral reactivation. Further studies examining the role of specific organisms that were shown to be correlative and predictive in viral reactivation, a serious problem in astronauts during spaceflight, could lead to mitigation strategies to help prevent disease during both short and long duration space missions. |
format | Online Article Text |
id | pubmed-7171750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71717502020-04-24 The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation Urbaniak, Camilla Lorenzi, Hernan Thissen, James Jaing, Crystal Crucian, Brian Sams, Clarence Pierson, Duane Venkateswaran, Kasthuri Mehta, Satish Microbiome Research BACKGROUND: Spaceflight impacts astronauts in many ways but little is known on how spaceflight affects the salivary microbiome and the consequences of these changes on astronaut health, such as viral reactivation. In order to understand this, the salivary microbiome was analyzed with 16S rRNA gene amplicon sequencing, and saliva viral titers were analyzed with quantitative polymerase chain reaction (qPCR) with primers specific for Epstein-Barr virus (EBV), herpes simplex virus (HSV), and varicella zoster virus (VZV) from 10 astronauts pre-flight, in-flight, and post-flight. RESULTS: Streptococcus was the most abundant organism in the saliva, making up 8% of the total organisms detected, and their diversity decreased during spaceflight. Other organisms that had statistically significant changes were Proteobacteria and Fusobacteria which increased during flight and Actinobacteria which decreased during flight. At the genus level, Catonella, Megasphera, and Actinobacillus were absent in more than half of saliva samples collected pre-flight but were then detected during flight. In those subjects that already had these genera pre-flight, their relative abundances increased during flight. Correlation analyses between the microbiome and viral titers revealed a positive correlation with Gracilibacteria, Absconditabacteria, and Abiotrophia and a negative correlation between Oribacterium, Veillonella, and Haemophilus. There was also a significant positive correlation between microbiome richness and EBV viral titers. CONCLUSIONS: This is the first study to look at how the salivary microbiome changes as a result of spaceflight and the search for bacterial biomarkers for viral reactivation. Further studies examining the role of specific organisms that were shown to be correlative and predictive in viral reactivation, a serious problem in astronauts during spaceflight, could lead to mitigation strategies to help prevent disease during both short and long duration space missions. BioMed Central 2020-04-20 /pmc/articles/PMC7171750/ /pubmed/32312311 http://dx.doi.org/10.1186/s40168-020-00830-z 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 Urbaniak, Camilla Lorenzi, Hernan Thissen, James Jaing, Crystal Crucian, Brian Sams, Clarence Pierson, Duane Venkateswaran, Kasthuri Mehta, Satish The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation |
title | The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation |
title_full | The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation |
title_fullStr | The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation |
title_full_unstemmed | The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation |
title_short | The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation |
title_sort | influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171750/ https://www.ncbi.nlm.nih.gov/pubmed/32312311 http://dx.doi.org/10.1186/s40168-020-00830-z |
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