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Visualization of Pseudomonas aeruginosa within the Sputum of Cystic Fibrosis Patients
Published on: July 16, 2020
Detection of pathogenic bacteria and biomarkers in lung specimens from cystic fibrosis patients
James J Tolle1, Samadhan Jadhao2,3, Brijesh Patel1
1Department of Medicine, Division of Allergy, Pulmonary & Critical Care Medicine, Nashville, TN, United States of America.
Abstract:
Diagnosing lung infections is often challenging because of the lack of a high-quality specimen from the diseased lung. Since persons with cystic fibrosis are subject to chronic lung infection, there is frequently a need for a lung specimen. In this small, proof of principle study, we determined that PneumoniaCheckTM, a non-invasive device that captures coughed droplets from the lung on a filter, might help meet this need. We obtained 10 PneumoniaCheckTMcoughed specimens and 2 sputum specimens from adult CF patients hospitalized with an exacerbation of their illness. We detected amylase (upper respiratory tract) with an enzymatic assay, surfactant A (lower respiratory tract) with an immunoassay, pathogenic bacteria by PCR, and markers of inflammation by a Luminex multiplex immunoassay. The amylase and surfactant A levels suggested that 9/10 coughed specimens were from lower respiratory tract with minimal upper respiratory contamination. The PCR assays detected pathogenic bacteria in 7 of 9 specimens and multiplex Luminex assay detected a variety of cytokines or chemokines. These data indicate that the PneumoniaCheckTMcoughed specimens can capture good quality lower respiratory tract specimens that have the potential to help in diagnosis, management and understanding of CF exacerbations and other lung disease.
Insights
PneumoniaCheck™, a non-invasive device, collects lung droplets for diagnosing infections. This study shows it captures high-quality lower respiratory specimens from cystic fibrosis patients, aiding in diagnosis and management.
Area of Science:
- Pulmonary Medicine
- Medical Diagnostics
- Microbiology
Background:
- Diagnosing lung infections is difficult due to poor specimen quality.
- Cystic fibrosis (CF) patients frequently require lung specimens for chronic infections.
Purpose of the Study:
- To evaluate PneumoniaCheck™, a non-invasive device, for collecting lung specimens.
- To assess the quality and diagnostic potential of coughed droplets from CF patients.
Main Methods:
- Collected 10 PneumoniaCheck™ coughed specimens and 2 sputum specimens from hospitalized adult CF patients.
- Analyzed specimens for upper and lower respiratory tract markers (amylase, surfactant A).
- Detected pathogenic bacteria using PCR and inflammatory markers with Luminex multiplex immunoassay.
Main Results:
- 9/10 PneumoniaCheck™ specimens showed lower respiratory origin with minimal upper tract contamination.
- Pathogenic bacteria were identified in 7/9 specimens via PCR.
- Luminex assay detected various cytokines and chemokines, indicating inflammation.
Conclusions:
- PneumoniaCheck™ successfully captures high-quality lower respiratory tract specimens.
- These specimens hold potential for diagnosing and managing CF exacerbations and other lung diseases.
- This non-invasive method may improve lung infection diagnostics.
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