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Gene Expression of Pathogens in Simulated MicrogravityExtended exposure to radiation and microgravity in space has been linked to astronauts developing chronic diseases upon returning to Earth. The Gram-negative pathogen Serratia marcescens has been shown to potentially cause significant infections in humans and in insect models on Earth. Our recent findings also showed that S. marcescens shows an increase in virulence after a short period of growth in the spaceflight environment, which raises initiatives to find the correlation between space environment and the increased virulence. Because we know that the health of astronauts is immunocompromised in space, it is possible that the combination of increased bacterial virulence and the weakened immune system will cause astronauts to be more susceptible to chronic diseases in extended spaceflight. With 75% of human disease genes being conserved in the fruit fly Drosophila melanogaster, these insects act as an ideal model organism to study the human immune system. The high accessibility, low cost, high rate of reproductivity, and short lifespans of D. melanogaster facilitate efficient, high-quality research that seeks to understand altered virulence of this opportunistic pathogen. In this ground-based study, we will use a rotating wall vessel apparatus to simulate microgravity and determine how pathogenicity changes by evaluating differences in gene expression for S. marcescens between bacteria grown in simulated microgravity conditions and controls. We will compare the results of our findings to gene expression patterns in actual spaceflight samples of S. marcescens grown on the ISS (International Space Station) during a recent validation mission, to see if there are common mechanisms across our simulated microgravity and actual spaceflight microgravity samples that both show increased virulence in the fruit fly. With extended space travel in the foreseeable future, understanding how human physiology will be affected by these different factors will help mitigate risks and deaths.
Document ID
20180007523
Acquisition Source
Ames Research Center
Document Type
Presentation
Authors
Tran, Nhung (Mindy) H.
(California Univ. San Diego, CA, United States)
Gilbert, Rachel R.
(Universities Space Research Association (USRA) Moffett Field, CA, United States)
Bhattacharya, Sharmila
(NASA Ames Research Center Moffett Field, CA, United States)
Date Acquired
November 7, 2018
Publication Date
October 29, 2018
Subject Category
Life Sciences (General)
Report/Patent Number
ARC-E-DAA-TN57969
Report Number: ARC-E-DAA-TN57969
Meeting Information
Meeting: Annual Meeting American Society for Gravitational and Space Research (ASGSR)
Location: Bethesda, MD
Country: United States
Start Date: October 29, 2018
End Date: November 3, 2018
Sponsors: American Society for Gravitational and Space Research
Funding Number(s)
CONTRACT_GRANT: NNH15CO48B
CONTRACT_GRANT: NNA14AB82C
Distribution Limits
Public
Copyright
Public Use Permitted.
Keywords
spaceflight analogue
immunology
invertebrates
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