4.7 Article

Selective Detection of Legionella pneumophila Serogroup 1 and 5 with a Digital Photocorrosion Biosensor Using Antimicrobial Peptide-Antibody Sandwich Strategy

Journal

BIOSENSORS-BASEL
Volume 12, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/bios12020105

Keywords

cysteine-modified warnericin RK; antimicrobial peptides; anti-Legionella pneumophila polyclonal antibody; digital photocorrosion biosensor; GaAs; AlGaAs nanoheterostructures

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC) Strategic Partnership Grant [SPG-2016-494057]
  2. NSERC Discovery Grant [RGPIN-2020-05558]

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This study demonstrates the enhanced detection of Legionella pneumophila using a modified digital photocorrosion biosensor functionalized with cysteine-modified warnericin antimicrobial peptides and anti-L. pneumophila polyclonal antibodies. The combination of peptides and antibodies allows for highly specific and sensitive detection of L. pneumophila.
Rapid detection of Legionella pneumophila (L. pneumophila) is important for monitoring the presence of these bacteria in water sources and preventing the transmission of the Legionnaires' disease. We report improved biosensing of L. pneumophila with a digital photocorrosion (DIP) biosensor functionalized with an innovative structure of cysteine-modified warnericin antimicrobial peptides for capturing bacteria that are subsequently decorated with anti-L. pneumophila polyclonal antibodies (pAbs). The application of peptides for the operation of a biosensing device was enabled by the higher bacterial-capture efficiency of peptides compared to other traditional ligands, such as those based on antibodies or aptamers. At the same time, the significantly stronger affinity of pAbs decorating the L. pneumophila serogroup-1 (SG-1) compared to serogroup-5 (SG-5) allowed for the selective detection of L. pneumophila SG-1 at 50 CFU/mL. The results suggest that the attractive sensitivity of the investigated sandwich method is related to the flow of an extra electric charge between the pAb and a charge-sensing DIP biosensor. The method has the potential to offer highly specific and sensitive detection of L. pneumophila as well as other pathogenic bacteria and viruses.

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