Longitudinal multi-omics analysis of host microbiome architecture and immune responses during short-term spaceflight

Braden Tierney(Cornell University), JangKeun Kim(Cornell University), Eliah Overbey(Cornell University), Krista Ryon(Cornell University), Jonathan Foox(Cornell University), Maria A. Sierra(Cornell University), Chandrima Bhattacharya(Cornell University), Namita Damle(Cornell University), Deena Najjar(Albert Einstein College of Medicine), Jiwoon Park(Cornell University), J. Sebastian Garcia Medina(Cornell University), Nadia Houerbi(Cornell University), Cem Meydan(Cornell University), Jeremy Wain Hirschberg(Cornell University), Jake Qiu(Cornell University), Ashley S. Kleinman(Cornell University), Gabriel A. Al‐Ghalith, Matthew MacKay(Cornell University), Evan E. Afshin(Cornell University), Raja Dhir(University of Zurich), Joseph Borg(University of Malta), Christine Gatt(University of Malta), Nicholas J. B. Brereton(University College Dublin), Benjamin Readhead(Arizona State University), Semir Beyaz(Cold Spring Harbor Laboratory), Kasthuri Venkateswaran(Jet Propulsion Laboratory), Kelly Wiseman(Elements Biosciences (United States)), Juan Moreno(Elements Biosciences (United States)), Andrew M. Boddicker(Elements Biosciences (United States)), Junhua Zhao(Elements Biosciences (United States)), Bryan R. Lajoie(Elements Biosciences (United States)), Ryan T. Scott(Ames Research Center), Andrew Altomare(Elements Biosciences (United States)), Semyon Kruglyak(Elements Biosciences (United States)), Shawn Levy(Elements Biosciences (United States)), George M. Church(Harvard University), Christopher E. Mason(Cornell University)
Nature Microbiology
June 11, 2024
Cited by 69Open Access
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Abstract

Maintenance of astronaut health during spaceflight will require monitoring and potentially modulating their microbiomes. However, documenting microbial shifts during spaceflight has been difficult due to mission constraints that lead to limited sampling and profiling. Here we executed a six-month longitudinal study to quantify the high-resolution human microbiome response to three days in orbit for four individuals. Using paired metagenomics and metatranscriptomics alongside single-nuclei immune cell profiling, we characterized time-dependent, multikingdom microbiome changes across 750 samples and 10 body sites before, during and after spaceflight at eight timepoints. We found that most alterations were transient across body sites; for example, viruses increased in skin sites mostly during flight. However, longer-term shifts were observed in the oral microbiome, including increased plaque-associated bacteria (for example, Fusobacteriota), which correlated with immune cell gene expression. Further, microbial genes associated with phage activity, toxin-antitoxin systems and stress response were enriched across multiple body sites. In total, this study reveals in-depth characterization of microbiome and immune response shifts experienced by astronauts during short-term spaceflight and the associated changes to the living environment, which can help guide future missions, spacecraft design and space habitat planning.


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