The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation

Abstract 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 rRN...

Full description

Bibliographic Details
Main Authors: Camilla Urbaniak, Hernan Lorenzi, James Thissen, Crystal Jaing, Brian Crucian, Clarence Sams, Duane Pierson, Kasthuri Venkateswaran, Satish Mehta
Format: Article
Language:English
Published: BMC 2020-04-01
Series:Microbiome
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40168-020-00830-z
id doaj-fc2c71c35e474ec48308e27f53648f5a
record_format Article
spelling doaj-fc2c71c35e474ec48308e27f53648f5a2020-11-25T03:28:50ZengBMCMicrobiome2049-26182020-04-018111410.1186/s40168-020-00830-zThe influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivationCamilla Urbaniak0Hernan Lorenzi1James Thissen2Crystal Jaing3Brian Crucian4Clarence Sams5Duane Pierson6Kasthuri Venkateswaran7Satish Mehta8NASA Jet Propulsion Laboratory, California Institute of TechnologyDepartment of Infectious Diseases, J. Craig Venter InstituteLawrence Livermore National LaboratoryLawrence Livermore National LaboratoryNASA Johnson Space CenterNASA Johnson Space CenterNASA Johnson Space CenterNASA Jet Propulsion Laboratory, California Institute of TechnologyJES Tech, NASA Johnson Space CenterAbstract 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. Video abstract.http://link.springer.com/article/10.1186/s40168-020-00830-zSalivary microbiomeViral reactivationAstronaut microbiomeSpaceflightInternational space station
collection DOAJ
language English
format Article
sources DOAJ
author Camilla Urbaniak
Hernan Lorenzi
James Thissen
Crystal Jaing
Brian Crucian
Clarence Sams
Duane Pierson
Kasthuri Venkateswaran
Satish Mehta
spellingShingle Camilla Urbaniak
Hernan Lorenzi
James Thissen
Crystal Jaing
Brian Crucian
Clarence Sams
Duane Pierson
Kasthuri Venkateswaran
Satish Mehta
The influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation
Microbiome
Salivary microbiome
Viral reactivation
Astronaut microbiome
Spaceflight
International space station
author_facet Camilla Urbaniak
Hernan Lorenzi
James Thissen
Crystal Jaing
Brian Crucian
Clarence Sams
Duane Pierson
Kasthuri Venkateswaran
Satish Mehta
author_sort Camilla Urbaniak
title 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_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_sort influence of spaceflight on the astronaut salivary microbiome and the search for a microbiome biomarker for viral reactivation
publisher BMC
series Microbiome
issn 2049-2618
publishDate 2020-04-01
description Abstract 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. Video abstract.
topic Salivary microbiome
Viral reactivation
Astronaut microbiome
Spaceflight
International space station
url http://link.springer.com/article/10.1186/s40168-020-00830-z
work_keys_str_mv AT camillaurbaniak theinfluenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT hernanlorenzi theinfluenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT jamesthissen theinfluenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT crystaljaing theinfluenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT briancrucian theinfluenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT clarencesams theinfluenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT duanepierson theinfluenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT kasthurivenkateswaran theinfluenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT satishmehta theinfluenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT camillaurbaniak influenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT hernanlorenzi influenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT jamesthissen influenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT crystaljaing influenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT briancrucian influenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT clarencesams influenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT duanepierson influenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT kasthurivenkateswaran influenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
AT satishmehta influenceofspaceflightontheastronautsalivarymicrobiomeandthesearchforamicrobiomebiomarkerforviralreactivation
_version_ 1724582516758675456