Affiliation:
1. Sections of Clinical Microbiology
2. Institute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany
3. Molecular Pathology, Cleveland Clinic Foundation, Cleveland, Ohio
Abstract
ABSTRACT
The efficiencies of five commercially available nucleic acid extraction methods were evaluated for the recovery of a standardized inoculum of
Legionella pneumophila
in respiratory specimens (sputum and bronchoalveolar lavage [BAL] specimens). The concentrations of
Legionella
DNA recovered from sputa with the automated MagNA Pure (526,200 CFU/ml) and NucliSens (171,800 CFU/ml) extractors were greater than those recovered with the manual methods (i.e., Roche High Pure kit [133,900 CFU/ml], QIAamp DNA Mini kit [46,380 CFU/ml], and ViralXpress kit [13,635 CFU/ml]). The rank order was the same for extracts from BAL specimens, except that for this specimen type the QIAamp DNA Mini kit recovered more than the Roche High Pure kit.
Publisher
American Society for Microbiology
Reference23 articles.
1. Comparison of a New Quantitative
ompA
-Based Real-Time PCR TaqMan Assay for Detection of
Chlamydia pneumoniae
DNA in Respiratory Specimens with Four Conventional PCR Assays
2. Clarke, S. C. 2002. Nucleotide sequence-based typing of bacteria and the impact of automation. Bioessays24:858-862.
3. Heginbothom, M. L., J. T. Magee, and P. G. Flanagan. 2003. Evaluation of the Idaho Technology LightCycler PCR for the direct detection of Mycobacterium tuberculosis in respiratory specimens. Int. J. Tuberc. Lung Dis.7:78-83.
4. Rapid Diagnosis of Extrapulmonary Tuberculosis by PCR: Impact of Sample Preparation and DNA Extraction
5. Iinuma, Y., K. Senda, N. Fujihara, T. Saito, S. Takakura, M. Shimojima, T. Kudo, and S. Ichiyama. 2003. Comparison of the BDProbeTec ET system with the Cobas Amplicor PCR for direct detection of Mycobacterium tuberculosis in respiratory samples. Eur. J. Clin. Microbiol. Infect. Dis.22:368-371.
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