A Diagnostic Chip for the Colorimetric Detection of Legionella pneumophila in Less than 3 h at the Point of Need

Author:

Tsougeni Katerina1,Kanioura Anastasia1,Kastania Athina S.12ORCID,Ellinas Kosmas1ORCID,Stellas Antonios3,Constantoudis Vassilios23,Moschonas Galatios4,Andritsos Nikolaos D.4ORCID,Velonakis Manolis4,Petrou Panagiota S.12ORCID,Kakabakos Sotirios E.12ORCID,Gogolides Evangelos12ORCID,Tserepi Angeliki12

Affiliation:

1. Nanoplasmas P.C., “Lefkippos” Technology Park, Patriarchou Gregoriou E’ & 27 Neapoleos Str., P.O. Box 60037, Ag. Paraskevi, 153 41 Athens, Greece

2. National Centre for Scientific Research “Demokritos”, Patriarchou Gregoriou E’ & 27 Neapoleos Str., Ag. Paraskevi, 153 41 Athens, Greece

3. Nanometrisis P.C., “Lefkippos” Technology Park, Patriarchou Gregoriou E’ & 27 Neapoleos Str., P.O. Box 60037, Ag. Paraskevi, 153 41 Athens, Greece

4. Eurofins Athens Analysis Laboratories, 29 Nafpliou Str., Metamorfosi, 144 52 Athens, Greece

Abstract

Legionella pneumophila has been pinpointed by the World Health Organization as the highest health burden of all waterborne pathogens in the European Union and is responsible for many disease outbreaks around the globe. Today, standard analysis methods (based on bacteria culturing onto agar plates) need several days (~12) in specialized analytical laboratories to yield results, not allowing for timely actions to prevent outbreaks. Over the last decades, great efforts have been made to develop more efficient waterborne pathogen diagnostics and faster analysis methods, requiring further advancement of microfluidics and sensors for simple, rapid, accurate, inexpensive, real-time, and on-site methods. Herein, a lab-on-a-chip device integrating sample preparation by accommodating bacteria capture, lysis, and DNA isothermal amplification with fast (less than 3 h) and highly sensitive, colorimetric end-point detection of L. pneumophila in water samples is presented, for use at the point of need. The method is based on the selective capture of viable bacteria on on-chip-immobilized and -lyophilized antibodies, lysis, the loop-mediated amplification (LAMP) of DNA, and end-point detection by a color change, observable by the naked eye and semiquantified by computational image analysis. Competitive advantages are demonstrated, such as low reagent consumption, portability and disposability, color change, storage at RT, and compliance with current legislation.

Funder

European Regional Development Fund of the European Union and Greek national funds

Stavros Niarchos Foundation

Publisher

MDPI AG

Reference57 articles.

1. (2019, September 01). Available online: http://www.who.int/mediacentre/factsheets/fs285/en/.

2. Legionella thermalis sp. nov., isolated from hot spring water in Tokyo, Japan;Ishizaki;Microbiol. Immunol.,2016

3. Bai, L., Yang, W., and Li, Y. (2023). Clinical and Laboratory Diagnosis of Legionella pneumonia. Diagnostics, 13.

4. Resuscitation of viable but nonculturable Legionella pneumophila Philadelphia JR32 by Acanthamoeba castellanii;Steinert;Appl. Environ. Microbiol.,1997

5. (2024, March 27). Available online: https://www.ecdc.europa.eu/en/legionnaires-disease/facts.

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