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Histological Quantification to Determine Lung Fungal Burden in Experimental Aspergillosis
Published on: March 9, 2018
Aspergillus infections in cystic fibrosis
Jill King1, Shan F Brunel1, Adilia Warris1
1Institute of Medical Sciences, Aberdeen Fungal Group, University of Aberdeen, UK.
Abstract:
Patients with cystic fibrosis (CF) suffer from chronic lung infection and airway inflammation. Respiratory failure secondary to chronic or recurrent infection remains the commonest cause of death and accounts for over 90% of mortality. Bacteria as Staphylococcus aureus, Pseudomonas aeruginosa and Burkholderia cepacia complex have been regarded the main CF pathogens and their role in progressive lung decline has been studied extensively. Little attention has been paid to the role of Aspergillus spp. and other filamentous fungi in the pathogenesis of non-ABPA (allergic bronchopulmonary aspergillosis) respiratory disease in CF, despite their frequent recovery in respiratory samples. It has become more apparent however, that Aspergillus spp. may play an important role in chronic lung disease in CF. Research delineating the underlying mechanisms of Aspergillus persistence and infection in the CF lung and its link to lung deterioration is lacking. This review summarizes the Aspergillus disease phenotypes observed in CF, discusses the role of CFTR (cystic fibrosis transmembrane conductance regulator)-protein in innate immune responses and new treatment modalities.
Insights
Aspergillus fungi, often overlooked in cystic fibrosis (CF), may significantly contribute to lung disease progression. Further research is needed to understand fungal persistence and its impact on CF lung health.
Area of Science:
- Pulmonology
- Infectious Diseases
- Medical Mycology
Background:
- Cystic Fibrosis (CF) patients experience chronic lung infections and inflammation, with respiratory failure being the primary cause of mortality.
- Bacterial pathogens like Staphylococcus aureus and Pseudomonas aeruginosa are well-studied in CF, but the role of fungi, particularly Aspergillus spp., is less understood.
- Filamentous fungi, including Aspergillus spp., are frequently detected in CF respiratory samples, suggesting a potential role in non-allergic bronchopulmonary aspergillosis (non-ABPA) respiratory disease.
Purpose of the Study:
- To review the disease phenotypes associated with Aspergillus spp. in CF patients.
- To explore the mechanisms of Aspergillus persistence and infection in the CF lung.
- To discuss the role of the cystic fibrosis transmembrane conductance regulator (CFTR) protein in innate immunity and potential new treatment strategies.
Main Methods:
- Literature review summarizing current knowledge on Aspergillus spp. in CF.
- Discussion of Aspergillus disease phenotypes and their impact on CF lung health.
- Analysis of the CFTR protein's function in innate immune responses to fungal pathogens.
Main Results:
- Aspergillus spp. are frequently recovered from CF respiratory samples and may play a significant role in chronic lung disease.
- There is a lack of research on the mechanisms of Aspergillus persistence and its link to lung deterioration in CF.
- The CFTR protein's role in innate immunity against fungal infections requires further elucidation.
Conclusions:
- Aspergillus spp. represent a potentially significant, yet understudied, contributor to chronic lung disease in cystic fibrosis.
- Understanding the interaction between Aspergillus spp., CFTR function, and the immune system is crucial for developing effective therapeutic strategies.
- Further research into fungal pathogenesis in CF is warranted to improve patient outcomes and reduce mortality.
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