Cargando…
Microbiome dynamics during the HI-SEAS IV mission, and implications for future crewed missions beyond Earth
BACKGROUND: Human health is closely interconnected with its microbiome. Resilient microbiomes in, on, and around the human body will be key for safe and successful long-term space travel. However, longitudinal dynamics of microbiomes inside confined built environments are still poorly understood. He...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831191/ https://www.ncbi.nlm.nih.gov/pubmed/33487169 http://dx.doi.org/10.1186/s40168-020-00959-x |
_version_ | 1783641584377528320 |
---|---|
author | Mahnert, Alexander Verseux, Cyprien Schwendner, Petra Koskinen, Kaisa Kumpitsch, Christina Blohs, Marcus Wink, Lisa Brunner, Daniela Goessler, Theodora Billi, Daniela Moissl-Eichinger, Christine |
author_facet | Mahnert, Alexander Verseux, Cyprien Schwendner, Petra Koskinen, Kaisa Kumpitsch, Christina Blohs, Marcus Wink, Lisa Brunner, Daniela Goessler, Theodora Billi, Daniela Moissl-Eichinger, Christine |
author_sort | Mahnert, Alexander |
collection | PubMed |
description | BACKGROUND: Human health is closely interconnected with its microbiome. Resilient microbiomes in, on, and around the human body will be key for safe and successful long-term space travel. However, longitudinal dynamics of microbiomes inside confined built environments are still poorly understood. Herein, we used the Hawaii Space Exploration Analog and Simulation IV (HI-SEAS IV) mission, a 1 year-long isolation study, to investigate microbial transfer between crew and habitat, in order to understand adverse developments which may occur in a future outpost on the Moon or Mars. RESULTS: Longitudinal 16S rRNA gene profiles, as well as quantitative observations, revealed significant differences in microbial diversity, abundance, and composition between samples of the built environment and its crew. The microbiome composition and diversity associated with abiotic surfaces was found to be rather stable, whereas the microbial skin profiles of individual crew members were highly dynamic, resulting in an increased microbiome diversity at the end of the isolation period. The skin microbiome dynamics were especially pronounced by a regular transfer of the indicator species Methanobrevibacter between crew members within the first 200 days. Quantitative information was used to track the propagation of antimicrobial resistance in the habitat. Together with functional and phenotypic predictions, quantitative and qualitative data supported the observation of a delayed longitudinal microbial homogenization between crew and habitat surfaces which was mainly caused by a malfunctioning sanitary facility. CONCLUSIONS: This study highlights main routes of microbial transfer, interaction of the crew, and origins of microbial dynamics in an isolated environment. We identify key targets of microbial monitoring, and emphasize the need for defined baselines of microbiome diversity and abundance on surfaces and crew skin. Targeted manipulation to counteract adverse developments of the microbiome could be a highly important strategy to ensure safety during future space endeavors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-020-00959-x. |
format | Online Article Text |
id | pubmed-7831191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78311912021-01-26 Microbiome dynamics during the HI-SEAS IV mission, and implications for future crewed missions beyond Earth Mahnert, Alexander Verseux, Cyprien Schwendner, Petra Koskinen, Kaisa Kumpitsch, Christina Blohs, Marcus Wink, Lisa Brunner, Daniela Goessler, Theodora Billi, Daniela Moissl-Eichinger, Christine Microbiome Research BACKGROUND: Human health is closely interconnected with its microbiome. Resilient microbiomes in, on, and around the human body will be key for safe and successful long-term space travel. However, longitudinal dynamics of microbiomes inside confined built environments are still poorly understood. Herein, we used the Hawaii Space Exploration Analog and Simulation IV (HI-SEAS IV) mission, a 1 year-long isolation study, to investigate microbial transfer between crew and habitat, in order to understand adverse developments which may occur in a future outpost on the Moon or Mars. RESULTS: Longitudinal 16S rRNA gene profiles, as well as quantitative observations, revealed significant differences in microbial diversity, abundance, and composition between samples of the built environment and its crew. The microbiome composition and diversity associated with abiotic surfaces was found to be rather stable, whereas the microbial skin profiles of individual crew members were highly dynamic, resulting in an increased microbiome diversity at the end of the isolation period. The skin microbiome dynamics were especially pronounced by a regular transfer of the indicator species Methanobrevibacter between crew members within the first 200 days. Quantitative information was used to track the propagation of antimicrobial resistance in the habitat. Together with functional and phenotypic predictions, quantitative and qualitative data supported the observation of a delayed longitudinal microbial homogenization between crew and habitat surfaces which was mainly caused by a malfunctioning sanitary facility. CONCLUSIONS: This study highlights main routes of microbial transfer, interaction of the crew, and origins of microbial dynamics in an isolated environment. We identify key targets of microbial monitoring, and emphasize the need for defined baselines of microbiome diversity and abundance on surfaces and crew skin. Targeted manipulation to counteract adverse developments of the microbiome could be a highly important strategy to ensure safety during future space endeavors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-020-00959-x. BioMed Central 2021-01-24 /pmc/articles/PMC7831191/ /pubmed/33487169 http://dx.doi.org/10.1186/s40168-020-00959-x Text en © The Author(s) 2021 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 Mahnert, Alexander Verseux, Cyprien Schwendner, Petra Koskinen, Kaisa Kumpitsch, Christina Blohs, Marcus Wink, Lisa Brunner, Daniela Goessler, Theodora Billi, Daniela Moissl-Eichinger, Christine Microbiome dynamics during the HI-SEAS IV mission, and implications for future crewed missions beyond Earth |
title | Microbiome dynamics during the HI-SEAS IV mission, and implications for future crewed missions beyond Earth |
title_full | Microbiome dynamics during the HI-SEAS IV mission, and implications for future crewed missions beyond Earth |
title_fullStr | Microbiome dynamics during the HI-SEAS IV mission, and implications for future crewed missions beyond Earth |
title_full_unstemmed | Microbiome dynamics during the HI-SEAS IV mission, and implications for future crewed missions beyond Earth |
title_short | Microbiome dynamics during the HI-SEAS IV mission, and implications for future crewed missions beyond Earth |
title_sort | microbiome dynamics during the hi-seas iv mission, and implications for future crewed missions beyond earth |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831191/ https://www.ncbi.nlm.nih.gov/pubmed/33487169 http://dx.doi.org/10.1186/s40168-020-00959-x |
work_keys_str_mv | AT mahnertalexander microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT verseuxcyprien microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT schwendnerpetra microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT koskinenkaisa microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT kumpitschchristina microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT blohsmarcus microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT winklisa microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT brunnerdaniela microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT goesslertheodora microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT billidaniela microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth AT moissleichingerchristine microbiomedynamicsduringthehiseasivmissionandimplicationsforfuturecrewedmissionsbeyondearth |