Molecular epidemiology of Aspergillus collected from cystic fibrosis patients

Raquel Sabino1, Jose A G Ferreira2, Richard B Moss3

  • 1National Institute of Health Dr. Ricardo Jorge-Infectious Diseases Department, Lisbon, Portugal; Department of Medicine, Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA, United States; California Institute for Medical Research, San Jose, CA, United States.

Abstract

Insights

Aspergillus fumigatus is the predominant species causing respiratory infections in cystic fibrosis (CF) patients. This study highlights its unique suitability for chronic colonization in CF airways, guiding future therapeutic strategies.

Area of Science:

  • Medical Mycology
  • Infectious Diseases
  • Pulmonology

Background:

  • Aspergillus respiratory infections are frequent in cystic fibrosis (CF).
  • These infections lead to pulmonary function decline and allergic conditions.
  • Understanding Aspergillus species prevalence is crucial for CF patient management.

Purpose of the Study:

  • To prospectively identify Aspergillus species colonizing the airways of cystic fibrosis patients.
  • To investigate the species diversity and prevalence of Aspergillus in CF respiratory infections.
  • To determine if cryptic Aspergillus species are prevalent in CF patients.

Main Methods:

  • Molecular identification of Aspergillus isolates using Internal Transcribed Spacer Region (ITS), β-tubulin, and calmodulin gene sequencing.
  • Analysis of 53 Aspergillus isolates obtained from cystic fibrosis patients.
  • Species-level identification of all isolates.

Main Results:

  • Aspergillus fumigatus sensu stricto was the most prevalent species (51 isolates).
  • Limited presence of other species, including Aspergillus terreus and Aspergillus niger.
  • No cryptic species of Aspergillus were detected in this cohort.

Conclusions:

  • Aspergillus fumigatus sensu stricto demonstrates a specific association with cystic fibrosis airways.
  • The unique characteristics of A. fumigatus likely facilitate its chronic residence in the CF lung.
  • Findings may inform targeted epidemiological and therapeutic strategies for Aspergillus-related CF complications.

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,...
1.1K
Fungal Phylum Ascomycota01:28

Fungal Phylum Ascomycota

Phylum Ascomycota, a major division within the subkingdom Dikarya, comprises a diverse range of fungal species, including both unicellular yeasts and filamentous molds such as Aspergillus and Penicillium. These fungi thrive in a variety of habitats, from aquatic ecosystems to terrestrial environments, playing crucial ecological and economic roles.Morphology and ReproductionThe defining characteristic of Ascomycetes, commonly referred to as sac fungi, is the ascus—a sac-like structure that...
2.5K
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...
656