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Journal of Clinical Microbiology, 10 1995, 2675-2678, Vol 33, No. 10
KB Register, MR Ackermann and DW Dyer
Current methods for the isolation and identification of Bordetella
bronchiseptica from clinical samples are time-consuming and are based, in
part, on subjective observations. We describe the use of a
Bordetella-specific DNA probe in a nonradioactive colony lift-
hybridization assay for the identification of B. bronchiseptica. Eleven of
82 clinical specimens were found to contain B. bronchiseptica by this
method, while only 5 of these were reported to contain the organism when
the specimens were analyzed by traditional methods. The chromosomal
fragment containing a sequence complementary to the probe appeared to be
conserved in B. bronchiseptica isolates from swine from a variety of
sources. The assay is more rapid than culture and biochemical testing since
it can be performed directly on primary culture plates, even when they are
heavily contaminated with other bacterial species. Only minimal training is
required to accomplish the assay successfully, and the results are easy to
interpret.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Nonradioactive colony lift-hybridization assay for detection of Bordetella bronchiseptica infection in swine
Swine Respiratory Diseases Project, National Animal Disease Center, U.S. Department of Agriculture, Ames, Iowa 50010, USA.
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