| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2091133 | Journal of Microbiological Methods | 2007 | 8 Pages |
In the present study, immunomagnetic separation of Legionella pneumophila from mock bronchoalveolar lavage (BAL) fluid samples, which were artificially spiked with L. pneumophila, and culture positive patient BAL fluid samples, was achieved using BioMags (superparamagnetic particles) loaded with purified rabbit immunoglobulin G specific for L. pneumophila. Bacteria binding onto BioMag-immunomatrix were directly stained with a L. pneumophila species-specific DFA reagent and examined under a fluorescence microscope. BioMag-based immunomagnetic separation (BIMS) followed by DFA staining (BIMS–DFA) could correctly identify all the 20 (100%) BAL samples which were spiked with low numbers (2 × 102 CFU) of L. pneumophila. Cultures could be recovered from 15 (75%) of these 20 spiked BAL samples, 5 (25%) of the samples failed to yield positive cultures. Both culture and BIMS–DFA methods showed 100% positive results when spiked BAL samples containing high bacterial load (104 CFU) were tested. The findings with true patient culture positive BAL specimens which were examined retrospectively indicated that BIMS–DFA is significantly more sensitive for detecting L. pneumophila than conventional cytospin method of DFA staining (cytospin–DFA). Out of the 25 culture positive BAL specimens tested, 7 (28%) proved negative by cytospin–DFA whereas BIMS–DFA correctly detected all the 25 (100%) specimens. It is suggested that the BIMS–DFA procedure increases the sensitivity of DFA testing for L. pneumophila in large volume samples such as BAL fluids.
