Molecular epidemiology and genetic determinants of β-lactam resistance in Pseudomonas aeruginosa isolates from patients with cystic fibrosis in Stockholm, Sweden
Year: 2026
Type: article
Abstract: Objectives Pseudomonas aeruginosa (PA), an opportunistic Gram-negative pathogen, is a leading cause of severe pulmonary infections in individuals with cystic fibrosis (CF). A significant proportion of patients become chronically infected, with negative consequences on respiratory function. Repeated or long-time suppressive antimicrobial treatment is often necessary, promoting development of antimicrobial resistance. Certain clones are particularly successful because of enhanced transmissibility and resistance development. We aimed to characterize the molecular epidemiology and genomic basis of β-lactam resistance in PA isolates from patients with CF in Sweden. Methods We performed whole genome sequencing and genomic characterization of 26 PA isolates collected from patients with CF at Karolinska University Hospital, Sweden. Results We identified the epidemic CF clone AUST-03 (ST242) and observed a high prevalence of multidrug- and extensively drug-resistant strains. Chromosomal mutations drove β-lactam resistance, with OprD porin loss (20 of 26, 77%) causing carbapenem resistance and potential production of extended-spectrum AmpC (9 of 26, 35%) conferring cephalosporin resistance, aligned with phenotypic susceptibility testing. Mutations in penicillin-binding protein 3 and bla AmpC repressors were prevalent. Notably, cefiderocol-resistant CF isolates had putative loss-of-function mutations in some iron metabolism–associated genes not found in cefiderocol-susceptible isolates, suggesting their role in resistance. Conclusions The results highlight the burden of antimicrobial resistance in CF-associated PA, distinct genetic determinants of resistance and the spread of epidemic clone AUST-03 in Swedish patients with CF. These insights can inform antimicrobial therapy and infection control measures.
Authors: Elin Loo, Chaitanya Tellapragada, Mohammad Razavi, Christian G. Giske
Institutions: Karolinska University Hospital, Karolinska Institutet
Language: English
Subfield: Molecular Medicine
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $3,780
Funder: Hjärt-Lungfonden
Award: G2801125203
OpenAlex ID: W7151249029
