한빛사논문
Braden T. Tierney 1,2,18, JangKeun Kim 1,2,18, Eliah G. Overbey 1,2,3,4, Krista A. Ryon 1, Jonathan Foox 1, Maria A. Sierra 5, Chandrima Bhattacharya 5, Namita Damle 1, Deena Najjar 1,6, Jiwoon Park 1,2, J. Sebastian Garcia Medina 1,2,5, Nadia Houerbi 1,2, Cem Meydan 1,2, Jeremy Wain Hirschberg 1, Jake Qiu 1, Ashley S. Kleinman 1, Gabriel A. Al-Ghalith 7, Matthew MacKay 5, Evan E. Afshin 1,2, Raja Dhir 7,8, Joseph Borg 9, Christine Gatt 9, Nicholas Brereton 10, Benjamin P. Readhead 11, Semir Beyaz 12, Kasthuri J. Venkateswaran 13, Kelly Wiseman 14, Juan Moreno 14, Andrew M. Boddicker 14, Junhua Zhao 14, Bryan R. Lajoie 14, Ryan T. Scott 15, Andrew Altomare 14, Semyon Kruglyak 14, Shawn Levy 14, George M. Church 16 & Christopher E. Mason 1,2,3,17,*
1Department of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA.
2The HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsaud Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, USA.
3BioAstra, Inc., New York, NY, USA.
4Center for STEM, University of Austin, Austin, TX, USA.
5Tri-Institutional Biology and Medicine program, Weill Cornell Medicine, New York, NY, USA.
6Albert Einstein College of Medicine, Bronx, NY, USA.
7Seed Health, Inc., Venice, CA, USA.
8Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich, Davos, Switzerland.
9Department of Applied Biomedical Science, Faculty of Health Sciences, University of Malta, Msida, Malta.
10School of Biology and Environmental Science, University College Dublin, Dublin, Ireland.
11ASU-Banner Neurodegenerative Disease Research Center, Arizona State University, Tempe, AZ, USA.
12Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.
13Jet Propulsion Laboratory, California Institute of Technology, Pasadena, CA, USA.
14Element Biosciences, San Diego, CA, USA.
15KBR; Space Biosciences Division, NASA Ames Research Center, Moffett Field, CA, USA.
16Harvard Medical School and the Wyss Institute, Boston, MA, USA.
17The WorldQuant Initiative for Quantitative Prediction, Weill Cornell Medicine, New York, NY, USA.
18These authors contributed equally: Braden T. Tierney, JangKeun Kim.
*Corresponding author: correspondence to Christopher E. Mason
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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