Evaluation of different primers for DNA fingerprinting of Legionella pneumophila serogroup 1 strains by the polymerase chain reaction

Wiese, Jutta, Helbig, J.H., Lück, C., Meyer, H.-G.W, Jansen, B. and Dunkelberg, H. (2004) Evaluation of different primers for DNA fingerprinting of Legionella pneumophila serogroup 1 strains by the polymerase chain reaction International Journal of Medical Microbiology, 294 (6). pp. 401-406. DOI 10.1016/j.ijmm.2004.07.006.

[img] Text
991_Wiese_2004_EvaluationOfDifferentPrimersFor_Artzeit_pubid6064.pdf - Published Version
Restricted to Registered users only

Download (232Kb) | Contact

Supplementary data:


A DNA fingerprinting method for the characterization of Legionella pneumophila serogroup I strains was established. This method was based on the DNA extraction using Chelex 100 and subsequent PCR analysis using primers under conditions of low stringency. Sixteen single primers were tested for the typing of the 10 epidemiologically unrelated reference strains of L. pneumophila serogroup I as well as patient isolates and environmental strains isolated from the water system of a hospital where patients with legionellosis were treated. In addition, a combination of two primers (Lpm-1 and Lpm-2) originally established for the specific detection of Legionella strains was tested. The PCR results were compared with two further subtyping methods, i.e. monoclonal antibody analysis and pulsed-field gel electrophoresis. The type strains Philadelphia 1, Knoxville 1, Allentown 1, Benidorm 0303E, Bellingham 1, and France 5811 could be distinguished clearly in experiments using all of the primers. Depending on the primer used, Heysham 1 and Oxford 4032E showed different DNA profiles. The strains Olda and Camperdown I were nearly indistinguishable. In contrast, the analysis by PFGE and MAb subtyping revealed distinct types for all 10 reference strains. The discrimination of the patient isolates from two suspected cases of nosocomial legionellosis and environmental isolates was not possible with the 16 single primers used in the study. However, the PCR assay with the combination of Lpm-1 and Lpm-2 as well as the PFGE and MAb analysis were able to differentiate distinct types. The use of the sequence-specific primers under low-stringency annealing conditions allowed both simultaneous gene detection as well as epidemiological typing of Legionella strains.

Document Type: Article
Additional Information: WOS:000225465200006
Research affiliation: OceanRep > GEOMAR > FB3 Marine Ecology > FB3-MI Marine Microbiology
Refereed: Yes
DOI etc.: 10.1016/j.ijmm.2004.07.006
ISSN: 1438-4221
Date Deposited: 11 Feb 2010 10:03
Last Modified: 23 May 2017 10:19
URI: http://eprints.uni-kiel.de/id/eprint/3311

Actions (login required)

View Item View Item

Document Downloads

More statistics for this item...