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Clinical and Diagnostic Laboratory Immunology, 01 1994, 44-50, Vol 1, No. 1
LC Lim, YF Liu, K Schell, SD Lovrich, SM Callister and RF Schell
Borreliacidal antibody has been shown to be important for the serodiagnosis
of Lyme disease and determination of immune status. Our results show that
borreliacidal antibody can be rapidly and accurately detected by flow
cytometry. Acridine orange was added to normal and immune sera containing
Borrelia burgdorferi organisms in the presence and absence of complement
prior to data acquisition by flow cytometry. The flow cytometric parameters
of side scatter and detection of acridine orange fluorescence were used to
determine events per minute (number of labeled spirochetes), percent shift
in fluorescence (number of dead spirochetes), and mean channel fluorescence
(intensity of fluorescence-labeled spirochetes) of acridine orange-labeled
spirochetes. Borreliacidal antibody was detected as early as 4 h, with
optimal detection 16 to 24 h after incubation of B. burgdorferi organisms
with immune serum and complement. Our results also showed that complement
was necessary for detection of borreliacidal antibody. Flow cytometry with
acridine orange-labeled spirochetes provides a rapid means for detection of
borreliacidal antibody.
Copyright © 1994 by the American Society for Microbiology. All rights reserved.
Detection of borreliacidal antibody by using acridine orange and flow cytometry
Wisconsin State Laboratory of Hygiene, University of Wisconsin, Madison 53706, USA.
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