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Applied and Environmental Microbiology, November 1998, p. 4234-4237, Vol. 64, No. 11
Institute for Hygiene and Infectious Diseases
of Animals, Justus-Liebig University, Giessen, Germany
Received 8 April 1998/Accepted 12 August 1998
For PCR detection of Coxiella burnetii in various
clinical specimens we developed a sample preparation method in which
silica binding of DNA was used. This method was found to be fast,
easily performed with large numbers of samples, and equally sensitive for all of the specimens tested (livers, spleens, placentas, heart valves, milk, blood). The DNA preparation method described here can
also be used as an initial step in any PCR-based examination of
specimens. The procedure was tested with more than 600 milk samples,
which were taken from 21 cows that were seropositive for C. burnetii and reportedly had fertility problems (and therefore were suspected of shedding the agent through milk intermittently or
continuously). Of the 21 cows tested, 6 were shedding C. burnetii through milk. Altogether, C. burnetii DNA
was detected in 6% of the samples. There was no correlation between
the shedding pattern and the serological results.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
PCR Detection of Coxiella burnetii from
Different Clinical Specimens, Especially Bovine Milk, on the Basis
of DNA Preparation with a Silica Matrix
*
Corresponding author. Mailing address: Institute for
Hygiene and Infectious Diseases of Animals, Frankfurter Str. 89, D-35392 Giessen, Germany. Phone: (49) 641 99 38308. Fax: (49) 641 99 38309. E-mail:
Hermann.Willems{at}vetmed.uni-giessen.de.
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