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Journal of Clinical Microbiology, May 1995, 1247-1252, Vol 33, No. 5
D Jonas, A Rosenbaum, S Weyrich and S Bhakdi
A nonradioactive method is described that detects 10 to 100 legionellae in
1 ml of bronchoalveolar lavage fluid. DNA is purified by a proteinase
K-phenol protocol or with a commercial DNA preparation kit and amplified by
PCR with amplimers specific for the 16S rRNA gene of Legionella
pneumophila. The upstream primer is 5' biotinylated. The amplification
product is immobilized on streptavidin-coated microtiter plates. Because of
the high binding capacity, no removal of nonincorporated biotin from the
PCR product is required. After alkaline denaturation, the single-stranded
PCR product is hybridized with a 5' digoxigenin-labeled probing oligomer.
The amplification product is then detected by using peroxidase-labeled
anti-digoxigenin antibodies in a luminescence or colorimetric reaction. The
assay detects as few as 10 legionellae in 1-ml bronchoalveolar lavage fluid
specimens. It is specific for medically relevant Legionella species,
including Legionella pneumophila, L. bozemanii, and L. longbeachae. Of over
250 clinical specimens examined, 8 were positive for legionellae by both
culture and the PCR assay. Six further specimens were culture negative but
PCR positive for legionellae; of these, five specimens were from patients
receiving high-dose erythromycin therapy for suspected or previously
diagnosed legionella pneumonia. None of the remaining 240 specimens that
were culture negative for legionellae yielded a positive PCR test, although
a total of over 30 different bacterial species were cultured from these
specimens. The PCR assay therefore appears to exhibit high sensitivity and
specificity and thus could prove suitable for use in the routine
microbiological diagnostic laboratory.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Enzyme-linked immunoassay for detection of PCR-amplified DNA of legionellae in bronchoalveolar fluid
Institute of Medical Microbiology and Hygiene, University of Mainz, Germany.
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