Appl. Environ. Microbiol., May 1997, 1643-1646, Vol 63, No. 5
MR Blake and BC Weimer
There are currently no methods for the rapid and sensitive detection of
bacterial spores that could be used to direct raw materials containing high
spore loads away from products that pose a food safety risk. Existing
methods require an overnight incubation, cannot detect spores below 10(5)
CFU/ml, or are not specific to particular species. This work describes a
method to specifically detect < 10(4) CFU of bacterial spores per ml
within 2 h. Polyclonal antibodies to Bacillus stearothermophilus spores
were attached to 2.8-micron-diameter magnetic polystyrene beads by using a
polythreonine cross-linker via the antibody carbohydrate moiety. A
biotin-avidin-amplified sandwich enzyme- linked immunosorbent assay coupled
to a fluorescent substrate was used to quantitate captured spores. The
concentration of B. stearothermophilus spores in samples was linearly
correlated to fluorescent activity (r2 = 0.99) with a lower detection limit
of 8 x 10(3) CFU/ml and an upper detection limit of 8 x 10(5) CFU/ml. The
detection limits are not fixed and can be changed by varying the
immunomagnetic bead concentration. Several food and environmental samples
were tested to demonstrate the versatility of the assay.
Copyright © 1997, American Society for Microbiology
Immunomagnetic detection of Bacillus stearothermophilus spores in food and environmental samples
Department of Nutrition and Food Sciences, Utah State University, Logan 84322, USA.
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