Investigation of Conditions for Capture of Live <i>Legionella pneumophila</i> with Polyclonal and Recombinant Antibodies
Lucas Paladines,
Walid M. Hassen,
Juliana Chawich,
Stefan Dübel,
Simon Lévesque,
Jan J. Dubowski,
Eric H. Frost
Affiliations
Lucas Paladines
Laboratory for Nano-Technologies and Nano-Characterization (LN2)-CNRS UMI-3463, Interdisciplinary Institute for Technological Innovation (3IT), Université de Sherbrooke, 3000 Boul. de l’Université, Sherbrooke, QC J1K 0A5, Canada
Walid M. Hassen
Laboratory for Nano-Technologies and Nano-Characterization (LN2)-CNRS UMI-3463, Interdisciplinary Institute for Technological Innovation (3IT), Université de Sherbrooke, 3000 Boul. de l’Université, Sherbrooke, QC J1K 0A5, Canada
Juliana Chawich
Laboratory for Nano-Technologies and Nano-Characterization (LN2)-CNRS UMI-3463, Interdisciplinary Institute for Technological Innovation (3IT), Université de Sherbrooke, 3000 Boul. de l’Université, Sherbrooke, QC J1K 0A5, Canada
Stefan Dübel
Department of Biotechnology, Technische Universität Braunschweig, Spielmannstrasse 7, 38106 Braunschweig, Germany
Simon Lévesque
Department of Microbiology and Infectiology, Faculty of Medicine and Health Science, Université de Sherbrooke, 3001 12th Avenue North, Sherbrooke, QC J1H 5N4, Canada
Jan J. Dubowski
Laboratory for Nano-Technologies and Nano-Characterization (LN2)-CNRS UMI-3463, Interdisciplinary Institute for Technological Innovation (3IT), Université de Sherbrooke, 3000 Boul. de l’Université, Sherbrooke, QC J1K 0A5, Canada
Eric H. Frost
Laboratory for Nano-Technologies and Nano-Characterization (LN2)-CNRS UMI-3463, Interdisciplinary Institute for Technological Innovation (3IT), Université de Sherbrooke, 3000 Boul. de l’Université, Sherbrooke, QC J1K 0A5, Canada
Since Legionella pneumophila has caused punctual epidemics through various water systems, the need for a biosensor for fast and accurate detection of pathogenic bacteria in industrial and environmental water has increased. In this report, we evaluated conditions for the capture of live L. pneumophila on a surface by polyclonal antibodies (pAb) and recombinant antibodies (recAb) targeting the bacterial lipopolysaccharide. Using immunoassay and PCR quantification, we demonstrated that, when exposed to live L. pneumophila in PBS or in a mixture containing other non-target bacteria, recAb captured one third fewer L. pneumophila than pAb, but with a 40% lower standard deviation, even when using the same batch of pAb. The presence of other bacteria did not interfere with capture nor increase background by either Ab. Increased reproducibility, as manifested by low standard deviation, is a characteristic that is coveted for biosensing. Hence, the recAb provided a better choice for immune adhesion in biosensors even though it was slightly less sensitive than pAb. Polyclonal or recombinant antibodies can specifically capture large targets such as whole bacteria, and this opens the door to multiple biosensor approaches where any of the components of the bacteria can then be measured for detection or characterisation.