Achromobacter spp. genetic adaptation in cystic fibrosis

Microb Genom. 2021 Jul;7(7):000582. doi: 10.1099/mgen.0.000582.

Abstract

Achromobacter spp. are emerging pathogens in patients with cystic fibrosis (CF) and Achromobacter spp. caused infections are associated with more severe disease outcomes and high intrinsic antibiotic resistance. While conventional CF pathogens are studied extensively, little is known about the genetic determinants leading to antibiotic resistance and the genetic adaptation in Achromobacter spp. infections. Here, we analysed 101 Achromobacter spp. genomes from 51 patients with CF isolated during the course of up to 20 years of infection to identify within-host adaptation, mutational signatures and genetic variation associated with increased antibiotic resistance. We found that the same regulatory and inorganic ion transport genes were frequently mutated in persisting clone types within and between Achromobacter species, indicating convergent genetic adaptation. Genome-wide association study of six antibiotic resistance phenotypes revealed the enrichment of associated genes involved in inorganic ion transport, transcription gene enrichment in β-lactams, and energy production and translation gene enrichment in the trimethoprim/sulfonamide group. Overall, we provide insights into the pathogenomics of Achromobacter spp. infections in patients with CF airways. Since emerging pathogens are increasingly recognized as an important healthcare issue, our findings on evolution of antibiotic resistance and genetic adaptation can facilitate better understanding of disease progression and how mutational changes have implications for patients with CF.

Keywords: Achromobacter; GWAS; cystic fibrosis airway infection; genomic adaptation; host-pathogen interaction; microbial genomics; within-host evolution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Achromobacter / drug effects
  • Achromobacter / genetics*
  • Achromobacter / isolation & purification
  • Adaptation, Physiological / genetics*
  • Cystic Fibrosis / microbiology*
  • Denmark
  • Disease Progression
  • Drug Resistance, Multiple, Bacterial / genetics*
  • Energy Metabolism / genetics
  • Genome, Bacterial / genetics
  • Genome-Wide Association Study
  • Gram-Negative Bacterial Infections / drug therapy
  • Gram-Negative Bacterial Infections / microbiology*
  • Host-Pathogen Interactions
  • Humans
  • Respiratory Tract Infections / drug therapy
  • Respiratory Tract Infections / microbiology*