Cefiderocol susceptibility of Achromobacter spp.: study of an accurately identified collection of 230 strains

Author:

Jean-Pierre Vincent,Sorlin Pauline,Pantel Alix,Chiron Raphaël,Lavigne Jean-Philippe,Jeannot Katy,Marchandin Hélène, ,Amara Marlène,Cadot Lucile,Dauwalder Olivier,Degand Nicolas,Demar Magalie,Dupin Clarisse,Fangous Marie-Sarah,Franczak Claire,Garnier Fabien,Guiet Pascal,Guinard Jérôme,Hombrouck-Alet Cécile,Kaoula Atika,Mariani-Kurkdjian Patricia,Nørskov-Lauritsen Niels,Schramm Frédéric,Tellini Charlotte,Texier Anthony,Violette Jérémie,Wilhelm Nathalie

Abstract

Abstract Background Achromobacter spp. are opportunistic pathogens, mostly infecting immunocompromised patients and patients with cystic fibrosis (CF) and considered as difficult-to-treat pathogens due to both intrinsic resistance and the possibility of acquired antimicrobial resistance. Species identification remains challenging leading to imprecise descriptions of resistance in each taxon. Cefiderocol is a broad-spectrum siderophore cephalosporin increasingly used in the management of Achromobacter infections for which susceptibility data remain scarce. We aimed to describe the susceptibility to cefiderocol of a collection of Achromobacter strains encompassing different species and isolation sources from CF or non-CF (NCF) patients. Methods We studied 230 Achromobacter strains (67 from CF, 163 from NCF patients) identified by nrdA gene-based analysis, with available susceptibility data for piperacillin–tazobactam, meropenem and trimethoprim–sulfamethoxazole. Minimal inhibitory concentrations (MICs) of cefiderocol were determined using the broth microdilution reference method according to EUCAST guidelines. Results Strains belonged to 15 species. A. xylosoxidans represented the main species (71.3%). MICs ranged from ≤ 0.015 to 16 mg/L with MIC50/90 of ≤ 0.015/0.5 mg/L overall and 0.125/2 mg/L against 27 (11.7%) meropenem-non-susceptible strains. Cefiderocol MICs were not related to CF/NCF origin or species although A. xylosoxidans MICs were statistically lower than those of other species considered as a whole. Considering the EUCAST non-species related breakpoint (2 mg/L), 228 strains (99.1%) were susceptible to cefiderocol. The two cefiderocol-resistant strains (A. xylosoxidans from CF patients) represented 3.7% of meropenem-non-susceptible strains and 12.5% of MDR strains. Conclusions Cefiderocol exhibited excellent in vitro activity against a large collection of accurately identified Achromobacter strains, irrespective of species and origin.

Publisher

Springer Science and Business Media LLC

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