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GROWTH AND SURVIVAL OF BACTERIA IN SIMULATED MARTIAN CONDITIONS
Title
GROWTH AND SURVIVAL OF BACTERIA IN SIMULATED MARTIAN CONDITIONS.
Creator
Berry, Bonnie, Jenkins, David, University of Central Florida
Abstract / Description
Escherichia coli and Serratia liquefaciens, two common microbial spacecraft contaminants known to replicate under low atmospheric pressures of 25 mb, were tested for growth and survival in simulated martian conditions. Stressors of high salinity, low temperature, and low pressure were screened alone and in combination to determine how they might affect microbial activity. Growth and survival of E. coli and S. liquefaciens under low temperatures (30, 20, 10, or 5 °C) with increasing...
Show moreEscherichia coli and Serratia liquefaciens, two common microbial spacecraft contaminants known to replicate under low atmospheric pressures of 25 mb, were tested for growth and survival in simulated martian conditions. Stressors of high salinity, low temperature, and low pressure were screened alone and in combination to determine how they might affect microbial activity. Growth and survival of E. coli and S. liquefaciens under low temperatures (30, 20, 10, or 5 °C) with increasing concentrations (0, 5, 10, or 20 %) of three salts believed to be present on the surface of Mars (MgCl2, MgSO4, NaCl) were monitored over 7 d. Results indicated higher growth rates for E. coli and S. liquefaciens at 30 and 20 °C and in solutions without salt or in 5 % concentrations. No increase in cell density occurred under the highest salt concentrations at any temperatures tested; however, survival rates were high, especially at 10 and 5 °C. Growth rates of E. coli and S. liquefaciens with and without salts at 1013, 100, or 25 mb of total atmospheric pressure were robust under all pressures. In a final experiment, E. coli was maintained in Mars-simulant soils in a Mars Simulation Chamber. Temperatures within the chamber were changed diurnally from -50 °C to 20 °C; UV light was present during daytime operation (8 hrs), and pressure was held at a constant 7.1 mb in a Mars atmosphere for 7 d. Results from the full-scale Mars simulation indicated that E. coli failed to increase its populations under simulated Mars conditions, but was not killed off by the low pressure, low temperature, or high salinity conditions. Escherichia coli, and potentially other bacteria from Earth, may be able to survive on Mars. Surviving bacteria may interfere with scientific studies or, if future conditions become more favorable for microbial growth, modify the martian atmosphere and biogeochemistry.
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Date Issued
2008
Identifier
CFE0002273, ucf:47856
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFE0002273
Development of human and rodent based in vitro systems toward better translation of bench to bedside in vivo results
Title
Development of human and rodent based in vitro systems toward better translation of bench to bedside in vivo results.
Creator
Berry, Bonnie, Hickman, James, Khaled, Annette, Lambert, Stephen, Sugaya, Kiminobu, University of Central Florida
Abstract / Description
Prospective medicinal compounds progress through multiple testing phases before becoming licensed drugs. Testing of novel compounds includes a preclinical phase where the potential therapeutic is tested in vitro and/or in animal models in vivo to predict its potential efficacy and/or toxicity in humans. The failure of preclinical models to accurately predict human drug responses can lead to potentially dangerous compounds being administered to humans, or potentially beneficial compounds being...
Show moreProspective medicinal compounds progress through multiple testing phases before becoming licensed drugs. Testing of novel compounds includes a preclinical phase where the potential therapeutic is tested in vitro and/or in animal models in vivo to predict its potential efficacy and/or toxicity in humans. The failure of preclinical models to accurately predict human drug responses can lead to potentially dangerous compounds being administered to humans, or potentially beneficial compounds being kept in development abeyance. Moreover, inappropriate choice in model organism for studying disease states may result in pushing forward inappropriate drug targets and/or compounds and wasting valuable time and resources in producing much-needed medications. In this dissertation, models for basic science research and drug testing are investigated with the intention of improving current preclinical models in order to drive drugs to market faster and more efficiently. We found that embryonic rat hippocampal neurons, commonly used to study neurodegenerative disease mechanisms in vitro, take 3-4 weeks to achieve similar, critical ion-channel expression profiles as seen in adult rat hippocampal cultures. We also characterized a newly-available commercial cell line of human induced pluripotent stem cell-derived neurons for their applicability in long-term studies, and used them to develop a more pathologically relevant model of early Alzheimer's Disease in vitro. Finally, we attempted to create an engineered, layered neural network of human neurons to study drug responses and synaptic mechanisms. Utilization of the results and methods described herein will help push forward the development of better model systems for translation of laboratory research to successful clinical human drug trials.
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Date Issued
2015
Identifier
CFE0006261, ucf:51031
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFE0006261