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Research Containing: Microbial contamination

Microbial monitoring of crewed habitats in space-current status and future perspectives

by cfynanon 9 June 2015in Biology & Biotechnology No comment

Previous space research conducted during short-term flight experiments and long-term environmental monitoring on board orbiting space stations suggests that the relationship between humans and microbes is altered in the crewed habitat in space. Both human physiology and microbial communities adapt to spaceflight. Microbial monitoring is critical to crew safety in long-duration space habitation and the sustained operation of life support systems on space transit vehicles, space stations, and surface habitats. To address this critical need, space agencies including NASA (National Aeronautics and Space Administration), ESA (European Space Agency), and JAXA (Japan Aerospace Exploration Agency) are working together to develop and implement specific measures to monitor, control, and counteract biological contamination in closed-environment systems. In this review, the current status of microbial monitoring conducted in the International Space Station (ISS) as well as the results of recent microbial spaceflight experiments have been summarized and future perspectives are discussed.

Related URLs:
http://www.ncbi.nlm.nih.gov/pubmed/25130885

Microbial contamination monitoring and control during human space missions

by cfynanon 9 June 2015in Biology & Biotechnology No comment

The ubiquity and resilience of microorganisms makes them unavoidable in most environments including space habitats. The impaired immune system of astronauts in flight raises the level of concern about disease risk during human space missions and additionally these biological contaminants may affect life support systems and hardware. In this review, the microbial contamination observed in manned space stations and in particular the International Space Station ISS will be discussed, demonstrating that it is a microbiologically safe working and living habitat. Microbial contamination levels were in general below the implemented quality standards, although, occasional contamination hazard reports indicate that the current prevention and monitoring strategies are the strict minimum.

Related URLs:
http://www.sciencedirect.com/science/article/pii/S0032063311002765

Microbial monitoring of spacecraft and associated environments

by cfynanon 9 June 2015in Biology & Biotechnology No comment

Rapid microbial monitoring technologies are invaluable in assessing contamination of spacecraft and associated environments. Universal and widespread elements of microbial structure and chemistry are logical targets for assessing microbial burden. Several biomarkers such as ATP, LPS, and DNA (ribosomal or spore-specific), were targeted to quantify either total bioburden or specific types of microbial contamination. The findings of these assays were compared with conventional, culture-dependent methods. This review evaluates the applicability and efficacy of some of these methods in monitoring the microbial burden of spacecraft and associated environments. Samples were collected from the surfaces of spacecraft, from surfaces of assembly facilities, and from drinking water reservoirs aboard the International Space Station (ISS). Culture-dependent techniques found species of Bacillus to be dominant on these surfaces. In contrast, rapid, culture-independent techniques revealed the presence of many Gram-positive and Gram-negative microorganisms, as well as actinomycetes and fungi. These included both cultivable and noncultivable microbes, findings further confirmed by DNA-based microbial detection techniques. Although the ISS drinking water was devoid of cultivable microbes, molecular-based techniques retrieved DNA sequences of numerous opportunistic pathogens. Each of the methods tested in this study has its advantages, and by coupling two or more of these techniques even more reliable information as to microbial burden is rapidly obtained.

Related URLs:
http://www.ncbi.nlm.nih.gov/pubmed/14749906

Spaceflight promotes biofilm formation by Pseudomonas aeruginosa

by cfynanon 9 June 2015in Biology & Biotechnology No comment

Understanding the effects of spaceflight on microbial communities is crucial for the success of long-term, manned space missions. Surface-associated bacterial communities, known as biofilms, were abundant on the Mir space station and continue to be a challenge on the International Space Station. The health and safety hazards linked to the development of biofilms are of particular concern due to the suppression of immune function observed during spaceflight. While planktonic cultures of microbes have indicated that spaceflight can lead to increases in growth and virulence, the effects of spaceflight on biofilm development and physiology remain unclear. To address this issue, Pseudomonas aeruginosa was cultured during two Space Shuttle Atlantis missions: STS-132 and STS-135, and the biofilms formed during spaceflight were characterized. Spaceflight was observed to increase the number of viable cells, biofilm biomass, and thickness relative to normal gravity controls. Moreover, the biofilms formed during spaceflight exhibited a column-and-canopy structure that has not been observed on Earth. The increase in the amount of biofilms and the formation of the novel architecture during spaceflight were observed to be independent of carbon source and phosphate concentrations in the media. However, flagella-driven motility was shown to be essential for the formation of this biofilm architecture during spaceflight. These findings represent the first evidence that spaceflight affects community-level behaviors of bacteria and highlight the importance of understanding how both harmful and beneficial human-microbe interactions may be altered during spaceflight.

Related URLs:
http://www.ncbi.nlm.nih.gov/pubmed/23658630

Determination of colloidal and dissolved silver in water samples using colorimetric solid-phase extraction

by cfynanon 9 June 2015in Biology & Biotechnology No comment

The increase in bacterial resistance to antibiotics has led to resurgence in the use of silver as a biocidal agent in applications ranging from washing machine additives to the drinking water treatment system on the International Space Station (ISS). However, growing concerns about the possible toxicity of colloidal silver to bacteria, aquatic organisms and humans have led to recently issued regulations by the US EPA and FDA regarding the usage of silver. As part of an ongoing project, we have developed a rapid, simple method for determining total silver, both ionic (silver(I)) and colloidal, in 0.1–1 mg/L aqueous samples, which spans the ISS potable water target of 0.3–0.5 mg/L (total silver) and meets the US EPA limit of 0.1 mg/L in drinking water. The method is based on colorimetric solid-phase extraction (C-SPE) and involves the extraction of silver(I) from water samples by passage through a solid-phase membrane impregnated with the colorimetric reagent DMABR (5-[4-(dimethylamino)benzylidene]rhodanine). Silver(I) exhaustively reacts with impregnated DMABR to form a colored compound, which is quantified using a handheld diffuse reflectance spectrophotometer. Total silver is determined by first passing the sample through a cartridge containing Oxone, which exhaustively oxidizes colloidal silver to dissolved silver(I). The method, which takes less than 2 min to complete and requires only ∼1 mL of sample, has been validated through a series of tests, including a comparison with the ICP-MS analysis of a water sample from ISS that contained both silver(I) and colloidal silver. Potential earth-bound applications are also briefly discussed.

Related URLs:
http://www.sciencedirect.com/science/article/pii/S0039914009007632

Bacterial and fungal communities in BPS chambers and root modules

by cfynanon 9 June 2015in Biology & Biotechnology No comment

The PESTO (Photosynthetic Experiment System Testing and Operation) experiment flew in the Biomass Production System (BPS) to International Space Station (ISS) on STS-110 (Atlantis) April 8, 2002, and returned on STS-111 (Endeavour) June 19, 2002, after 73 days in space. The ground control was conducted on a two-week delay at Kennedy Space Center in a BPS unit under environmental conditions comparable to ISS. Wheat ( Triticum aestivum cv Apogee) and Brassica rapa cv Astroplant were independently grown in root modules for multiple grow-outs. On-orbit harvests, root modules exchanges and primings, seeds imbibitions, and gas and water samplings occurred at periodic intervals; all were replicated in ground controls. Many operations required crew handling and open access to individual chambers, allowing the exchange of microorganisms between the crew environment and the BPS modules. Upon landing, BPS surfaces, containment bags, root modules, and plant material were swabbed for recovery of microbes. Water samples were collected from BPS nutrient delivery and humidity control systems (HCS), root modules, and wastewater bags. Swabs and liquid samples were plated onto selective media; microbial and fungal colonies were identified to the species level by metabolic profiling when possible. Differences in bacterial and fungal species and the number of species identified were detected between the flight and ground controls.

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