TY - JOUR
T1 - Real-time in situ detection and quantification of bacteria in the Arctic environment
AU - Powers, Linda
AU - Ellis, Walther R.
AU - Lloyd, Christopher R.
N1 - Funding Information: This work was supported by AMASE under the NASA ASTEP program (A. Steele PI), the Thomas R. Brown Foundation, and the University of Arizona. The authors thank Hans Amundsen, Pam Conrad, Andrew Duncan, Miriam Eaton, Marc Fries, Michael Garrett, Steven Squyres, Andrew Steele and Lois Wardell for support during various phases of this work.
PY - 2014/3
Y1 - 2014/3
N2 - At present, there are no methods that determine the total microbial load on an abiotic substrate in real time. The utility of such a capability ranges from sterilization and medical diagnostics to the search for new microorganisms in the environment and study of their ecological niches. We report the development of a hand-held, fluorescence detection device and demonstrate its applicability to the field detection of Arctic bacteria. This technology is based on the early pioneering work of Britton Chance which elucidated the intrinsic fluorescence of a number of metabolites and protein cofactors in cells, including reduced pyridine nucleotides, cytochromes and flavins. A PDA controls the device (fluorescence excitation and data collection) and processes the multiwavelength signals to yield bacterial cell counts, including estimates of live cells, dead cells and endospores. Unlike existing methods for cell counting, this method requires no sample contact or addition of reagents. The use of this technology is demonstrated with in situ measurements of two sub-glacial microbial communities at sites in Palander and colonized surface rocks in the Bockfjord Volcanic Complex during AMASE 2008 (Arctic Mars Analog Svalbard Expedition). The total bacterial load on the interrogated sample surfaces ranged from < 20 cells/cm2 to > 109 cells/cm2.
AB - At present, there are no methods that determine the total microbial load on an abiotic substrate in real time. The utility of such a capability ranges from sterilization and medical diagnostics to the search for new microorganisms in the environment and study of their ecological niches. We report the development of a hand-held, fluorescence detection device and demonstrate its applicability to the field detection of Arctic bacteria. This technology is based on the early pioneering work of Britton Chance which elucidated the intrinsic fluorescence of a number of metabolites and protein cofactors in cells, including reduced pyridine nucleotides, cytochromes and flavins. A PDA controls the device (fluorescence excitation and data collection) and processes the multiwavelength signals to yield bacterial cell counts, including estimates of live cells, dead cells and endospores. Unlike existing methods for cell counting, this method requires no sample contact or addition of reagents. The use of this technology is demonstrated with in situ measurements of two sub-glacial microbial communities at sites in Palander and colonized surface rocks in the Bockfjord Volcanic Complex during AMASE 2008 (Arctic Mars Analog Svalbard Expedition). The total bacterial load on the interrogated sample surfaces ranged from < 20 cells/cm2 to > 109 cells/cm2.
KW - Intrinsic fluorescence
KW - Svalbard Archipelago
KW - amplitude modulation
KW - microbial sensor
KW - optical detection
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U2 - 10.1142/S1793545813500387
DO - 10.1142/S1793545813500387
M3 - Article
SN - 1793-5458
VL - 7
JO - Journal of Innovative Optical Health Sciences
JF - Journal of Innovative Optical Health Sciences
IS - 2
M1 - 1350038
ER -