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Water is a critical commodity for spacecraft crews, requiring extreme conservation and reclamation strategies. In addition to suppression of the immune system in spaceflight, enhancement of bacterial growth and antimicrobial resistance in weightlessness raise serious concerns regarding microbial contamination of water systems. Rapid methods are needed for monitoring water, both pre-flight and on orbit. We are developing techniques to enumerate specific, metabolically active bacteria that may threaten crew health or lead to water system deterioration. Our methods are directed at the detection of individual bacteria, rather than populations of bacteria, and we aim to determine the identity of the organism as well as its physiological state con-currently. Our objectives are to determine, in a single test, the total number of bacteria present in a water sample, if a specific strain of bacteria is present within the total population and if these bacteria are viable or dead.

To compare the disinfection susceptibility of mucoid and non-mucoid P. aeruginosa in relation to EPS production, cultures were grown to stationary phase in defined media with a high or low C/N ratio using glucose as carbon source. Cultures diluted with phosphate buffered water pH 7.2 were pretreated by vortexing, centrifuging, or blending with 10 mM EDTA in PBW before disinfection with iodine, chlorine or monochloramine. It is suggested that differences observed between disinfectants may be due to their reactivities with cell constituents or modes of action. EPS may play a significant role in bacterial resistance to iodine and other halogens, although susceptibility varies markedly in relation to nutrient status and sample treatment before disinfection.

To determine the microbiological quality of water for potable and other purposes, there is a need for rapid methods to enumerate viable bacteria. This is of particular importance for the proposed water recovery systems planned for the United States Space Station, in which wastewaters including hygiene water and urine will be reclaimed for potable use. Existing microbiological culture methods are limited by the time taken to obtain results and because it is not possible to detect the total microbial populations by these methods. We have been investigating direct microscopic methods which detect individual bacterial cells. Fluorogenic compounds are used which are taken up by active cells, permitting a direct assessment of physiological activity. The methods are being adapted for use with membrane filtration which permits concentration of small numbers of cells from large volumes of water. Procedures for direct examination of cells growing on surfaces as biofilms have also been devised.