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.

PubMed

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.

Related Concept Videos

Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
214
Cystic Fibrosis: Management01:24

Cystic Fibrosis: Management

Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
154
Serum Laboratory Studies, Stool Test, Breath Test01:30

Serum Laboratory Studies, Stool Test, Breath Test

Gastrointestinal (GI) diagnostic studies are pivotal in confirming, ruling out, diagnosing, or staging various diseases, including cancers. Following diagnosis, allocating time for discussions with the patient and providing informational resources is crucial. Diagnostic assessments of the GI tract often occur in outpatient settings like endoscopy suites or GI labs. Preparation for these tests may include dietary restrictions, fasting, liquid bowel preparations, laxatives, enemas, and the...
334
Sputum Studies I: Gram Stain, cytology, and Acid-fast smear and culture01:26

Sputum Studies I: Gram Stain, cytology, and Acid-fast smear and culture

Sputum studies are a critical part of diagnosing and treating numerous respiratory conditions. These studies involve obtaining sputum samples for analysis to identify pathogenic organisms and assess the presence of abnormal cells indicative of malignant conditions. This lesson will delve into three fundamental sputum studies: Gram Stain, Cytology, and Acid-fast Smear and Culture.
Gram Stain
The Gram Stain is an integral part of sputum studies. It involves the staining of sputum, which permits...
189