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Journal of Clinical Microbiology, August 2007, p. 2726-2730, Vol. 45, No. 8
0095-1137/07/$08.00+0 doi:10.1128/JCM.00321-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Christian Lück, and
Enno Jacobs
Technical University Dresden, Medical Faculty Carl Gustav Carus, Institute of Medical Microbiology and Hygiene, Fetscherstrasse 74, D-01307 Dresden, Germany
Received 9 February 2007/ Returned for modification 22 March 2007/ Accepted 18 May 2007
To enhance the sensitivity of the available real-time PCR systems for the detection of Mycoplasma pneumoniae, we established a method to amplify copies of the repetitive element repMp1. In a study of respiratory tract samples, we found that, compared to the use of the conserved part of the P1 adhesin gene as a monocopy target, the use of the repMp1-PCR showed an increase in the detected genome equivalents by a factor of 22.
Published ahead of print on 30 May 2007.
Present address: Swiss Federal Institute of Technology Zürich, Institute of Food Science and Nutrition, Schmelzbergstrasse 7, CH-8092 Zürich, Switzerland.
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