Abstract

ABSTRACTCystic fibrosis (CF) is a genetic disorder characterized by progressive lung function decline. CF patients are at an increased risk of respiratory infections, including those by the environmental bacterium Burkholderia pseudomallei, the causative agent of melioidosis. Here, we compared the genomes of B. pseudomallei isolates collected between ~4 and 55 months apart from seven chronically infected CF patients. Overall, the B. pseudomallei strains showed evolutionary patterns similar to those of other chronic infections, including emergence of antibiotic resistance, genome reduction, and deleterious mutations in genes involved in virulence, metabolism, environmental survival, and cell wall components. We documented the first reported B. pseudomallei hypermutators, which were likely caused by defective MutS. Further, our study identified both known and novel molecular mechanisms conferring resistance to three of the five clinically important antibiotics for melioidosis treatment. Our report highlights the exquisite adaptability of microorganisms to long-term persistence in their environment and the ongoing challenges of antibiotic treatment in eradicating pathogens in the CF lung. Convergent evolution with other CF pathogens hints at a degree of predictability in bacterial evolution in the CF lung and potential targeted eradication of chronic CF infections in the future.

Highlights

  • Cystic fibrosis (CF) is a genetic disorder characterized by progressive lung function decline

  • We show that the pathways by which B. pseudomallei adapts to the CF lung are similar to those seen in better-studied CF pathogens such as Pseudomonas aeruginosa, Staphylococcus aureus, and Burkholderia cepacia complex species

  • The pathophysiology of the CF lung greatly increases the risk of opportunistic bacterial infections, those caused by Pseudomonas aeruginosa, Haemophilus influenzae, Staphylococcus aureus, and various nonfermenting Gram-negative bacteria, including members of the Burkholderia cepacia complex (Bcc) [2]

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Summary

Introduction

Cystic fibrosis (CF) is a genetic disorder characterized by progressive lung function decline. We performed whole-genome sequencing (WGS) and comparative genomic analysis of sequential B. pseudomallei isolates from chronically infected CF patients to document within-host evolution.

Results
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