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PreprintCC BY-NCbioRxiv

Microbial Dynamics Across Commercial Spaceflights of Varying Duration

8 more authors
  1. 1Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA

Abstract

Spaceflight introduces environmental stressors that can alter human microbiomes and immune responses. We analyzed 259 and 17 biospecimens for microbiome and single-cell studies from n=6 astronauts across two commercial ISS missions: Axiom 2 (10-day mission) and Axiom 3 (21-day mission). Samples included saliva, stool, urine, and body swabs from 10 anatomical sites, profiled via 16S ribosomal RNA (rRNA) gene amplicon sequencing. Gut and oral microbiomes remained stable, while skin-associated communities exhibited transient diversity shifts post-flight. Taxonomic analysis revealed individual and site-specific patterns, as well as from the spaceflight/ISS environment. Cytokine profiling from single-cell data indicated immune activation, with IL-32 and IL-16 transcripts elevated in Axiom 2 and Axiom 3. Microbiome and interleukin correlation analyses found 14 significant associations in Axiom 2 data. These findings provide an integrated view of microbiome individuality. Our study represents a descriptive comparison of two missions, informing strategies for crew health on future long-duration missions.

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BibTeX
@misc{krishnavajhala2026microbial,
  title = {{Microbial Dynamics Across Commercial Spaceflights of Varying Duration}},
  author = {A. Krishnavajhala and M.-C. Gingras and T. Santiago-Rodriguez and Y. Chen and D. Bandaranaike and S. Bhamidipati and Q. Xiang and K. Kottapalli and Z. Momin and A. Santhanam and K. Walker and Q. Wang and S. M. Griffin and M. M. Masternak and M. C. Ross and D. Muzny and J. Wu and E. Urquieta and R. Gibbs and H. doddapaneni},
  howpublished = {bioRxiv},
  year = {2026},
  month = may,
  doi = {10.64898/2026.05.29.728784},
  url = {https://www.biorxiv.org/content/10.64898/2026.05.29.728784v2},
  note = {CC BY-NC},
}
RIS
TY  - UNPB
TI  - Microbial Dynamics Across Commercial Spaceflights of Varying Duration
AU  - A. Krishnavajhala
AU  - M.-C. Gingras
AU  - T. Santiago-Rodriguez
AU  - Y. Chen
AU  - D. Bandaranaike
AU  - S. Bhamidipati
AU  - Q. Xiang
AU  - K. Kottapalli
AU  - Z. Momin
AU  - A. Santhanam
AU  - K. Walker
AU  - Q. Wang
AU  - S. M. Griffin
AU  - M. M. Masternak
AU  - M. C. Ross
AU  - D. Muzny
AU  - J. Wu
AU  - E. Urquieta
AU  - R. Gibbs
AU  - H. doddapaneni
PY  - 2026
DA  - 2026/05/29
PB  - bioRxiv
DO  - 10.64898/2026.05.29.728784
UR  - https://www.biorxiv.org/content/10.64898/2026.05.29.728784v2
AB  - Spaceflight introduces environmental stressors that can alter human microbiomes and immune responses. We analyzed 259 and 17 biospecimens for microbiome and single-cell studies from n=6 astronauts across two commercial ISS missions: Axiom 2 (10-day mission) and Axiom 3 (21-day mission). Samples included saliva, stool, urine, and body swabs from 10 anatomical sites, profiled via 16S ribosomal RNA (rRNA) gene amplicon sequencing. Gut and oral microbiomes remained stable, while skin-associated communities exhibited transient diversity shifts post-flight. Taxonomic analysis revealed individual and site-specific patterns, as well as from the spaceflight/ISS environment. Cytokine profiling from single-cell data indicated immune activation, with IL-32 and IL-16 transcripts elevated in Axiom 2 and Axiom 3. Microbiome and interleukin correlation analyses found 14 significant associations in Axiom 2 data. These findings provide an integrated view of microbiome individuality. Our study represents a descriptive comparison of two missions, informing strategies for crew health on future long-duration missions.
ER  -