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Updated: Aug 16, 2026

Cystic Fibrosis Aggregate Biofilm Model to Study Infection-relevant Gene Expression
Published on: April 18, 2025
[Nontuberculous mycobacteria in cystic fibrosis]
M Le Bourgeois1, I Sermet-Gaudelus, E Catherinot
1Service de pneumologie pédiatrique, hôpital Necker-Enfants-malades, Assistance-publique-Hôpitaux-de Paris, 75015 Paris, France. muriel.lebourgeois@nck.aphp.fr
Abstract:
Patients with cystic fibrosis are particularly at risk of infection with non-tuberculous mycobacteria (NTM). Prevalence of these infections increases with age to around 15 %. The main species involved are M. abscessus and M. avium, the latter not found in children under 15. Diagnosis relies on clinical, radiological and above all bacteriological criteria defined by the ATS. Identification of the causal species of NTM is essential and requires genetic techniques, some of which are currently evaluated. Treatment depends on the mycobacterial species. For M. avium, combined therapy with rifampicin, clarithromycin and ethambutol must be extended 12 months after negativation. M. abscessus infection is particularly resistant to therapy. Usual treatment is a one month course of intravenous imipenem or cefoxitin plus amikacin followed by oral clarithromycin plus ethambutol for at least 12 months after negativation. In case of local lesions, surgery is an option.
Insights
Cystic fibrosis patients face a higher risk of non-tuberculous mycobacteria (NTM) infections, primarily M. abscessus and M. avium. Effective treatment requires species-specific, prolonged antimicrobial therapy and sometimes surgery.
Area of Science:
- Pulmonary Medicine
- Infectious Diseases
- Microbiology
Context:
- Cystic fibrosis (CF) patients exhibit increased susceptibility to non-tuberculous mycobacteria (NTM) infections.
- Prevalence of NTM infections in CF patients approaches 15%, with Mycobacterium abscessus and Mycobacterium avium being the predominant species.
- Diagnosis relies on integrated clinical, radiological, and bacteriological criteria, necessitating precise species identification.
Purpose:
- To outline the diagnostic criteria and treatment strategies for NTM infections in cystic fibrosis patients.
- To highlight the challenges and specific approaches for managing M. abscessus and M. avium infections.
Summary:
- NTM infections are a significant concern in cystic fibrosis, with prevalence increasing with age.
- Accurate identification of NTM species, often requiring advanced genetic techniques, is crucial for guiding therapy.
- Treatment regimens are species-dependent, involving prolonged combination antimicrobial therapy (e.g., rifampicin, clarithromycin, ethambutol for M. avium; imipenem/amikacin followed by clarithromycin/ethambutol for M. abscessus), with surgery considered for localized lesions.
Impact:
- Informed clinical decision-making for NTM management in CF.
- Improved understanding of species-specific treatment protocols for better patient outcomes.
- Potential for enhanced diagnostic accuracy through evaluation of genetic identification techniques.
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