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  2. Genomic insights and phenotypic characterization of three multidrug resistant Cupriavidus strains from the cystic fibrosis lung

Genomic insights and phenotypic characterization of three multidrug resistant Cupriavidus strains from the cystic fibrosis lung

  • J Appl Microbiol. 2025 May 2;136(5):lxaf093. doi: 10.1093/jambio/lxaf093.
Sean D Kelly 1 James Butler 1 Heather Green 2 Andrew M Jones 2 Dervla T D Kenna 3 Sumita Pai 4 Katie J Muddiman 1 Trudie A McComb 1 Briana M Barrand 1 Vicky Bennett 5 Gyorgy Fejer 1 Mathew Upton 1
Affiliations

Affiliations

  • 1 School of Biomedical Sciences, Faculty of Health, University of Plymouth, Drake Circus, Plymouth, Devon PL4 8AA, United Kingdom.
  • 2 Manchester Adult Cystic Fibrosis Centre, Wythenshawe Hospital, Southmoor Road, Wythenshawe, Manchester, Greater Manchester M23 9LT, United Kingdom.
  • 3 Public Health Microbiology Division, Specialised Microbiology and Laboratories Directorate, UK Health Security Agency, Colindale Avenue, London, Greater London NW9 5EQ, United Kingdom.
  • 4 Royal Papworth Hospital NHS Foundation Trust, Papworth Road, Cambridge, Cambridgeshire CB2 0AY, United Kingdom.
  • 5 Department of Life Sciences, University of Bath, Claverton Down, Bath, Somerset BA2 7AY, United Kingdom.
Abstract

Aims: We aimed to investigate phenotypic and genomic traits of three Cupriavidus spp. isolates recovered from people with cystic fibrosis (PWCF). These bacteria are recognized as emerging pathogens in PWCF.

Methods and results: Using short and long Sequencing reads, we assembled three hybrid complete genomes for the genus Cupriavidus, adding to the 45 published currently, describing multipartite genomes and plasmids. The isolates likely represent three different species, and they carry a cumulative total of 30 Antibiotic resistance genes with high homology to well-characterized resistance determinants from Other bacteria. Multidrug resistance to Antibiotics used in CF management was observed in all three isolates. However, two treatments were active across all isolates: cefotaxime and piperacillin/tazobactam. Biofilm formation was only seen at physiological temperatures (37°C) and lost at 20°C and all isolates had low lethality in Galleria mellonella larvae. Isolates demonstrated variable motility, with one non-motile isolate carrying a disrupted flhD transcriptional regulator, abolishing flagella expression.

Conclusions: Our Cupriavidus spp. isolates showed considerable genomic and phenotypic variability that may impact their virulence and treatment in PWCF, where multidrug resistance will negate treatments and biofilm formation and motility play key roles in Infection establishment, as seen in CF pathogens like Pseudomonas aeruginosa. More detailed investigation of clinical Cupriavidus isolates is needed for full understanding of the risk they pose to PWCF.

Keywords

biofilm; cupriavidus; cystic fibrosis; hybrid genome assembly; motility; multi-drug resistance.

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