Rapid Detection of Pseudomonas aeruginosa Biofilms via Enzymatic Liquefaction of Respiratory Samples

ACS Sens. 2020 Dec 24;5(12):3956-3963. doi: 10.1021/acssensors.0c01618. Epub 2020 Nov 24.

Abstract

Respiratory infections caused by multi-drug-resistant Pseudomonas aeruginosa often yield poor outcomes if not detected right away. However, detecting this pathogen in respiratory samples with a rapid diagnostic test is challenging because the protective biofilms created by the pathogen are themselves surrounded by a high-viscosity sputum matrix. Here, we introduce a method for liquefying respiratory samples and disrupting bacterial biofilms on the spot within a minute. It relies on the generation of oxygen bubbles by bacterial catalase through the addition of hydrogen peroxide. When coupled with a mobile biosensor made of paper, the resulting diagnostic kit was able to detect P. aeruginosa infections in sputa from patients with excellent sensitivity and specificity within 8 min. The quick turnaround time along with few infrastructure requirements make this method ideal for the rapid screening of P. aeruginosa infections at the point of care.

Keywords: bacteria; biosensor; catalase; colorimetric; immunosensor; pathogen; smartphone; sputum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteria
  • Biofilms*
  • Humans
  • Pseudomonas aeruginosa*
  • Sensitivity and Specificity
  • Sputum