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Mutators in cystic fibrosis chronic lung infection: Prevalence, mechanisms, and consequences for antimicrobial
1Instituto Universitario de Investigación en Ciencias de la Salud, Palma de Mallorca, Spain. antonio.oliver@ssib.es
Abstract:
Hypermutable (or mutator) microorganisms are those that have an increased spontaneous mutation rate due to defects in DNA repair or error avoidance systems. Over last decade, several studies have provided strong evidence of a relevant role of mutators in the evolution of natural bacterial populations, with a special emphasis in the field of infectious diseases. Among them, chronic respiratory infection by Pseudomonas aeruginosa in cystic fibrosis (CF) patients was the first natural environment revealing a high prevalence and important role of mutators. High frequencies of mutators have also been noted for other pathogens in the CF setting, particularly Staphylococcus aureus and Haemophilus influenzae. In addition to a strong statistical link between hypermutation and antibiotic resistance (i.e., mutators are more frequently resistant against antibiotics) obtained from the analysis of collections of clinical isolates from CF patients, several in vitro and in vivo experiments have further highlighted the dramatic consequences of hypermutation, especially when acting on microorganisms that are genetically equipped to acquire efficient resistance to most antibiotics by mutations in chromosomal genes such as P. aeruginosa. Recent studies additionally showed that mutators accelerate genetic adaptation of P. aeruginosa to the airways of CF patients and that patients infected by mutator strains have a poorer lung function. Further prospective clinical studies are nevertheless needed for a deep evaluation of the impact of mutators in disease progression and outcome. Future research should particularly focus on the investigation of the optimal therapeutical strategies to prevent the emergence of mutator strains in the lungs of CF patients and to avoid multiple-antimicrobial resistance development if they have already been selected.
Insights
Hypermutator microorganisms accelerate antibiotic resistance and adaptation in cystic fibrosis (CF) patients. Understanding mutator strains is crucial for developing effective treatments to combat infectious diseases in CF.
Area of Science:
- Microbiology
- Evolutionary Biology
- Infectious Diseases
Background:
- Hypermutable microorganisms exhibit elevated spontaneous mutation rates due to impaired DNA repair.
- Mutator strains play a significant role in the evolution of bacterial populations, particularly in infectious diseases.
- Chronic Pseudomonas aeruginosa infections in cystic fibrosis (CF) patients are a key environment where mutators are prevalent.
Purpose of the Study:
- To investigate the role and impact of hypermutator microorganisms in the context of infectious diseases, especially within the CF setting.
- To explore the link between hypermutation and the development of antibiotic resistance.
- To understand how mutator strains contribute to pathogen adaptation and disease progression in CF patients.
Main Methods:
- Analysis of clinical isolates from CF patients to determine the prevalence and characteristics of mutator strains.
- In vitro and in vivo experiments to assess the consequences of hypermutation on antibiotic resistance and adaptation.
- Review of recent studies examining the impact of mutator strains on P. aeruginosa adaptation to the CF airways.
Main Results:
- A strong statistical association exists between hypermutation and increased antibiotic resistance in CF patient isolates.
- Mutator strains, particularly P. aeruginosa, demonstrate accelerated genetic adaptation to the CF lung environment.
- Patients infected with mutator strains of P. aeruginosa exhibit poorer lung function.
Conclusions:
- Hypermutation significantly contributes to the evolution of antibiotic resistance and pathogen adaptation in CF infections.
- Mutator strains are linked to worse clinical outcomes in CF patients.
- Further research is needed to evaluate the clinical impact of mutators and to develop strategies to prevent their emergence and mitigate antimicrobial resistance.
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