TY - JOUR
T1 - Achromobacter spp. genetic adaptation in cystic fibrosis
AU - Gabrielaite, Migle
AU - Nielsen, Finn C
AU - Johansen, Helle K
AU - Marvig, Rasmus L
PY - 2021/7
Y1 - 2021/7
N2 - 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.
AB - 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.
KW - Achromobacter/drug effects
KW - Adaptation, Physiological/genetics
KW - Cystic Fibrosis/microbiology
KW - Denmark
KW - Disease Progression
KW - Drug Resistance, Multiple, Bacterial/genetics
KW - Energy Metabolism/genetics
KW - Genome, Bacterial/genetics
KW - Genome-Wide Association Study
KW - Gram-Negative Bacterial Infections/drug therapy
KW - Host-Pathogen Interactions
KW - Humans
KW - Respiratory Tract Infections/drug therapy
KW - GWAS
KW - Microbial genomics
KW - Host-pathogen interaction
KW - Genomic adaptation
KW - Cystic fibrosis airway infection
KW - Within-host evolution
KW - Achromobacter
UR - http://www.scopus.com/inward/record.url?scp=85111251915&partnerID=8YFLogxK
U2 - 10.1099/MGEN.0.000582
DO - 10.1099/MGEN.0.000582
M3 - Journal article
C2 - 34232117
SN - 2057-5858
VL - 7
JO - Microbial genomics
JF - Microbial genomics
IS - 7
M1 - 000582
ER -