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Microbial biofilm formation during space flight (Micro-2A)
03.22.12

Overview | Description | Applications | Operations | Results | Publications | Images

Experiment/Payload Overview

Brief Summary

Microbial biofilm formation during space flight (Micro-2A) studies how gravity alters biofilm formation. Biofilms are groups of microorganisms that form on surfaces. One goal of this experiment is to develop new strategies to reduce the impact of biofilms on crew health and to minimize the harmful effects of them on materials in space and on Earth.

Principal Investigator

  • Cynthia H. Collins, Ph.D., Rensselaer Polytechnic Institute, Troy, NY, United States
  • Co-Investigator(s)/Collaborator(s)

  • Joel L. Plawsky, Sc.D.,, Rensselaer Polytechnic Institute, Troy, NY, United States
  • Jonathan S. Dordick, Ph.D., Rensselaer Polytechnic Institute, Troy, NY, United States
  • Payload Developer

    University of Colorado at Boulder, BioServe Space Technologies, Boulder, CO, United States

    Sponsoring Space Agency

    National Aeronautics and Space Administration (NASA)

    Sponsoring Organization:

    Exploration Systems Mission Directorate (ESMD)

    ISS Expedition Duration:

    March 2011 - September 2011



    Expeditions Assigned

    27/28

    Previous ISS Missions

    Micro-2A builds on the results obtained from Micro-2 on STS-132, in the methods of cultivation of the organisms, the anti-microbial surfaces tested, and the mutant strains of the organisms used. The results from the STS-135 experiment not only complement the results obtained from STS-132 but also provide new data on the anti-biofilm action of additional surface coatings.

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    Experiment/Payload Description

    Research Summary

    • The Microbial biofilm formation during space flight (Micro-2A) investigation aims to understand the different responses and physical effects of reduced gravitational force on biofilm formation (complex aggregates of microorganisms attached to a surface). Cells grown in microgravity are compared to cells grown in normal gravity. The amount of biomass formed is measured and confocal microscopy (an optical imaging technique used to increase optical resolution and contrast) is used to identify changes in the three-dimensional structures of the biofilms. This study also tests a number of newly developed antimicrobial surfaces for their potential to reduce biofilm formation.


    • Understanding the different responses and physical effects of microgravity on biofilm formation may provide new insights into combating biofilm formation in space. Furthermore, this work may also lead to better management and treatment of infections in space and on Earth.

    Description

    The goal of Microbial biofilm formation during space flight (Micro-2A) is to understand the effects of microgravity on the growth, cellular physiology, and cell-cell interactions in microbial biofilms. It focuses on two model microorganisms that form biofilms both inside and outside of the human body, Pseudomonas aeruginosa and Staphylococcus aureus (S. aureus). These microbes can switch between benign (not harmful) and pathogenic (able to cause disease) interactions with humans and may be relevant to crew health during extended missions. This experiment also tests the ability of novel antimicrobial surfaces to reduce biofilm formation.

    When cells form biofilms they have a number of potentially harmful properties, including increased potential for infection and increased resistance to antimicrobial compounds. Biofilms have the potential to cause significant damage to both spacecraft and their crew; numerous problems caused by biofilms were documented on Mir. A greater understanding of the effects of spaceflight on biofilms is critical.

    The Micro-2A experiment makes use of Group Activation Packs (GAPs) stored in a Commercial Generic Bioprocessing Apparatus (CGBA). The CGBA is a flight certified incubator capable of controlling the temperature between 8ºC and 37ºC. Each GAP holds eight Fluid Processing Apparatus (FPA) inserts. The FPA is composed of a glass barrel divided into three chambers that are separated from one another by rubber septa. Each FPA contains growth medium with membranes in the first chamber, a microbial culture suspended in stasis medium in the second chamber, and a termination reagent in the last chamber.

    Micro-2A builds on the results obtained in the Micro-2 experiment flown on STS-132. Micro-2A utilizes new methods of cultivation of the organisms that should enhance the growth of S. aureus. In addition, the results from the STS-135 Micro-2A experiment also provide new data on the anti-biofilm action of additional surface coatings not used for Micro-2.

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    Applications

    Space Applications

    Understanding the different effects of microgravity on biofilm formation may provide new insights into combating biofilm formation in space and may lead to better management and treatment of infections if they occur. Also, novel antimicrobial surfaces are tested for their potential to reduce the impact of biofilms in future spacecraft design.

    Earth Applications

    According to the Center for Disease Control (CDC), hospital-acquired infections are the fourth leading cause of death in the United States behind stroke, cancer and heart disease. Furthermore, it is estimated that greater than 65 percent of all bacterial infections are associated with biofilms. A greater understanding of biofilms is essential if we are to find effective methods to combat their formation. Furthermore, the low-shear conditions microbes experience in microgravity are similar to those found in the human body that are difficult to study. This work may provide new insights into the role of shear and other physical effects, such as convection, on biofilm formation.

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    Operations

    Operational Requirements

    The Micro-2A experiment consists of 63 samples housed in 8 GAPs. The temperature profile of the CGBA and the temperature logger (HOBO) are required for the post-flight analysis of the data.

    Operational Protocols

    The samples are stowed in the CGBA at 8ºC until as late in the mission as possible then CGBA temperature is set to 37ºC and all GAPs are activated. To activate the samples, a crewmember must remove the CGBA from its middeck stowage location, take out each GAP and install the hand crank. The hand crank is then turned until the cell suspension in the second chamber is introduced to the growth media in the first chamber. Following the 72-hour growth period, a crewmember installs the hand crank again and terminates the GAPs by adding the termination reagent in the last chamber to the cells. Only a subset of the GAPs needs to be terminated. All GAPs are returned to the CGBA and the CGBA is set to 8ºC where it will remain until recovery.

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    Results/More Information

    Information Pending

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    Related Web Sites
  • Rensselaer Polytechnic Institute ? Collins Research Group
  • Space Biosciences Division ? Micro2 (STS-132)
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    Publications

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    Ground Based Results Publications

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    ISS Patent Publications

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    Related Publications

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    Images

    imageDr. Cynthia Collins, Rensselaer Polytechnic Institute, prepares samples for Microbial biofilm formation during space flight (Micro-2A). Image courtesy of NASA.


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    imageCommercial Generic Bioprocessing Apparatus (CGBA) that houses the Microbial biofilm formation during space flight (Micro-2A) samples. Image courtesy of NASA.


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    imageGroup activation Pack (GAP) containing Fluid Processing Apparatus (FPA) for Microbial biofilm formation during space flight (Micro-2A). Image courtesy of NASA.


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    Information provided by the investigation team to the ISS Program Scientist's Office.
    If updates are needed to the summary please contact JSC-ISS-Program-Science-Group. For other general questions regarding space station research and technology, please feel free to call our help line at 281-244-6187 or e-mail at JSC-ISS-Payloads-Helpline.