Annals of Clinical Microbiology and Antimicrobials (Nov 2024)

Transmission cluster of cefiderocol-non-susceptible carbapenem-resistant Acinetobacter baumannii in cefiderocol-naïve individuals

  • Claudia Alteri,
  • Antonio Teri,
  • Maria Francesca Liporace,
  • Antonio Muscatello,
  • Leonardo Terranova,
  • Margherita Carnevale Schianca,
  • Federica Salari,
  • Beatrice Silvia Orena,
  • Flaminia Gentiloni Silverj,
  • Mara Bernazzani,
  • Simona Biscarini,
  • Giulia Renisi,
  • Lisa Cariani,
  • Caterina Matinato,
  • Ciro Canetta,
  • Alessandra Bandera,
  • Annapaola Callegaro

DOI
https://doi.org/10.1186/s12941-024-00763-7
Journal volume & issue
Vol. 23, no. 1
pp. 1 – 6

Abstract

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Abstract Background During prolonged FDC therapy, the emergence of FDC non-susceptibility in CRAB has been reported. Here, we report a transmission cluster of FDC-non-susceptible CRAB in four patients, all naïve to FDC treatment, characterized by a premature stop codon and amino acid deletion in the PirA protein. Methods CRAB strains obtained from patients admitted in a single medicine ward of the IRCCS Fondazione Ospedale Maggiore Policlinico between March and July 2024 were analyzed by WGS and antimicrobial susceptibility testing. Phylogenetic analysis was used to assess their genetic relatedness. Results Between March and July 2024, an outbreak of 33 CRAB was observed among hospitalized patients in a single ward at IRCCS. Genomic analysis, available in 29 cases, revealed that 24 isolates belonged to ST208/1806, 4 to ST369, and one to ST195/1816 (according to the Oxford scheme). FDC susceptibility was affected only in the four ST369 isolates (Kirby-Bauer disk diffusion diameter: 13 mm; UMIC® method MIC: 4 mg/L), all characterized by a premature stop codon followed by a 52 amino acid deletion located between the amino acids 377 and 428 of the siderophore-drug receptor PirA. No other relevant mutations were detected in the iron-uptake genes. Core-genome ML tree including ST369 reference strains revealed that the four ST369 isolates were highly related and formed a distinct cluster (SNP distance: 3 [IQR: 1–6]). Of note, the four isolates were collected from four FDC-naïve individuals, two experiencing a CRAB-mediated infection. Conclusions Our findings alert about the circulation of clones carrying modified siderophore-drug receptors without evidence of previous FDC treatment and support the importance of testing FDC susceptibility appropriately before its administration.

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