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Spaceflight-Induced Changes in Microbial Virulence and the Impact to the Host Immune Response Many microbial pathogens have repeatedly exhibited unexpected responses relevant to infectious disease when grown in microgravity and microgravity analogue environments, including changes in final cell concentration, biofilm production, stress resistance, antibiotic sensitivity, gene expression, host-pathogen interactions, and virulence. Notably, the classic foodborne pathogen Salmonella enterica serovar Typhimurium displayed increased virulence in animals when cultured in either the spaceflight analogue or true spaceflight environment. Recently, Serratia marcescens also was shown to increase virulence when cultured in the spaceflight environment. In parallel, astronaut studies have characterized a persistent spaceflight-induced dysregulation of the human immune system at multiple levels, which suggests an increased risk of infectious diseases. Moreover, astronauts have some degree of clinical infectious disease incidence. However, the contribution of the microgravity environment on host-pathogen interactions and potential for clinical disease remains understudied and poorly characterized.

The goal of this study is to gain insight into the breadth of other medically significant microbial pathogens that may exhibit altered virulence and pathogenesis-related responses when cultured in spaceflight analogue conditions. Specifically, we are characterizing the effect of spaceflight analogue culture (Low Shear Modeled Microgravity/LSMMG) on microbial pathogenesis-related stress responses, in vitro host-pathogen interactions, gene expression, and virulence potential in animals using five important model bacterial pathogens, Salmonella enterica Enteritidis, Pseudomonas aeruginosa, Burkholderia cepacia, Streptococcus pneumoniae, and enterohemorrhagic Escherichia coli.

The information to date is providing a better understanding into the potential impact of microgravity on alterations in microbial virulence and associated infectious disease risk to crew health during spaceflight missions.
Document ID
20240012410
Acquisition Source
Johnson Space Center
Document Type
Abstract
Authors
C M Ott
(Johnson Space Center Houston, United States)
J Barrila ORCID
(Arizona State University Tempe, United States)
S Koroli
(Arizona State University Tempe, United States)
S Gangaraju
(Arizona State University Tempe, United States)
R R Davis
(Arizona State University Tempe, United States)
S G Thornhill
(JES Tech (United States) Houston, Texas, United States)
J Yang
(Arizona State University Tempe, United States)
K A Hoffman
(KBR (United States) Houston, Texas, United States)
R A Rice
(KBR (United States) Houston, Texas, United States)
A A Medina-Colorado
(KBR (United States) Houston, Texas, United States)
C Vu
(Arizona State University Tempe, United States)
B Y Kang ORCID
(Arizona State University Tempe, United States)
L L Banken
(Arizona State University Tempe, United States)
P Stafford ORCID
(Arizona State University Tempe, United States)
C Oubre
(Johnson Space Center Houston, United States)
B E Crucian
(Johnson Space Center Houston, United States)
C A Nickerson ORCID
(Arizona State University Tempe, United States)
Date Acquired
September 26, 2024
Subject Category
Aerospace Medicine
Meeting Information
Meeting: Human Research Program-Investigators Working Group (HRP-IWG) Workshop
Location: Galveston, TX
Country: US
Start Date: January 28, 2025
End Date: January 31, 2025
Sponsors: National Aeronautics and Space Administration
Funding Number(s)
WBS: 609524.07.02.03.02
CONTRACT_GRANT: NNJ15HK11B
CONTRACT_GRANT: 80JSC023DA004
Distribution Limits
Public
Copyright
Use by or on behalf of the US Gov. Permitted.
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