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Rapid and quantitative detection of Legionella pneumophila applying immunomagnetic separation and flow cytometry
Author(s) -
Füchslin Hans Peter,
Kötzsch Stefan,
Keserue HansAnton,
Egli Thomas
Publication year - 2010
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.20858
Subject(s) - legionella , legionella pneumophila , flow cytometry , immunomagnetic separation , microbiology and biotechnology , detection limit , chromatography , biology , bacteria , chemistry , genetics
Abstract Legionella is a pathogenic bacterium that establishes and proliferates well in water storage and distribution systems. Worldwide it is responsible for numerous outbreaks of legionellosis, which can be fatal. Despite recent advances in molecular and immunological methods, the official, internationally accepted detection method for Legionella spp. in water samples (ISO 11371) is still based on cultivation. This method has major disadvantages such as a long assay time of 10 days and the detection of cultivable cells only. Therefore, we developed a cultivation‐independent, quantitative, and fast detection method for Legionella pneumophila in water samples. It consists of four steps, starting with (1) a concentrating step, in which cells present in one litre of water are concentrated into 5 ml by filtration (pore size 0.45 μm), (2) then cells are resuspended with sterile filtered buffer and double‐stained with FITC‐ and Alexa‐conjugated Legionella ‐specific antibodies, (3) subsequently, the cells are immunomagnetically caught, and (4) finally, fluorescently labeled Legionella cells were flow cytometrically detected and quantified. The efficiency of each step was tested separately. The whole method allows detection of L. pneumophila in 180 min with a detection limit of around 500 cells/l and a recovery of Legionella cells of 52.1 % out of spiked tap water. Fluorescence microscopy and flow cytometric cell‐counting correlated well. © 2010 International Society for Advancement of Cytometry