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Published on: March 17, 2014
Hypermutator Pseudomonas aeruginosa Exploits Multiple Genetic Pathways To Develop Multidrug Resistance during
C A Colque1,2, A G Albarracín Orio1,2,3, S Feliziani1,2
1Universidad Nacional de Córdoba, Facultad de Ciencias Químicas, Departamento de Química Biológica Ranwel Caputto, Córdoba, Argentina.
Abstract:
Pseudomonas aeruginosa exploits intrinsic and acquired resistance mechanisms to resist almost every antibiotic used in chemotherapy. Antimicrobial resistance in P. aeruginosa isolates recovered from cystic fibrosis (CF) patients is further enhanced by the occurrence of hypermutator strains, a hallmark of chronic infections in CF patients. However, the within-patient genetic diversity of P. aeruginosa populations related to antibiotic resistance remains unexplored. Here, we show the evolution of the mutational resistome profile of a P. aeruginosa hypermutator lineage by performing longitudinal and transversal analyses of isolates collected from a CF patient throughout 20 years of chronic infection. Our results show the accumulation of thousands of mutations, with an overall evolutionary history characterized by purifying selection. However, mutations in antibiotic resistance genes appear to have been positively selected, driven by antibiotic treatment. Antibiotic resistance increased as infection progressed toward the establishment of a population constituted by genotypically diversified coexisting sublineages, all of which converged to multidrug resistance. These sublineages emerged by parallel evolution through distinct evolutionary pathways, which affected genes of the same functional categories. Interestingly, ampC and ftsI, encoding the β-lactamase and penicillin-binding protein 3, respectively, were found to be among the most frequently mutated genes. In fact, both genes were targeted by multiple independent mutational events, which led to a wide diversity of coexisting alleles underlying β-lactam resistance. Our findings indicate that hypermutators, apart from boosting antibiotic resistance evolution by simultaneously targeting several genes, favor the emergence of adaptive innovative alleles by clustering beneficial/compensatory mutations in the same gene, hence expanding P. aeruginosa strategies for persistence.
Insights
Pseudomonas aeruginosa hypermutators in cystic fibrosis patients accumulate mutations, driving parallel evolution towards multidrug resistance. This study reveals how genetic diversity and parallel evolution enhance antibiotic resistance in chronic infections.
Area of Science:
- Microbiology
- Evolutionary Biology
- Genetics
Background:
- Pseudomonas aeruginosa exhibits significant antibiotic resistance, exacerbated by hypermutator strains in cystic fibrosis (CF) patients.
- Within-patient genetic diversity of P. aeruginosa concerning antibiotic resistance remains poorly understood.
Purpose of the Study:
- To investigate the evolution of the mutational resistome profile of P. aeruginosa in a CF patient over 20 years.
- To understand the role of hypermutation and genetic diversity in the development of multidrug resistance.
Main Methods:
- Longitudinal and transversal analyses of P. aeruginosa isolates collected from a single CF patient over two decades.
- Characterization of the mutational landscape and evolutionary trajectories of antibiotic resistance genes.
Main Results:
- Thousands of mutations accumulated, with purifying selection overall, but positive selection in antibiotic resistance genes driven by treatment.
- Genotypically diversified sublineages emerged through parallel evolution, converging on multidrug resistance.
- ampC and ftsI genes were frequently mutated, showing diverse alleles contributing to beta-lactam resistance.
Conclusions:
- Hypermutators accelerate antibiotic resistance evolution by targeting multiple genes and promoting adaptive mutations.
- Parallel evolution of distinct sublineages contributes to P. aeruginosa's multidrug resistance and persistence strategies in CF patients.
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