Progressive in vivo development of resistance to cefiderocol in Pseudomonas aeruginosa.

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info:eu-repo/semantics/altIdentifier/doi/10.1007/s10096-022-04526-0

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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_5982A68F66EF2

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Pseudomonas pyocyanea

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M. Sadek et al., « Progressive in vivo development of resistance to cefiderocol in Pseudomonas aeruginosa. », Serveur académique Lausannois, ID : 10.1007/s10096-022-04526-0


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We report in vivo development of cefiderocol (FDC) resistance among four sequential Pseudomonas aeruginosa clinical isolates ST244 recovered from a single patient, without exposure to FDC, which raises concern about the effectiveness of this novel drug. The first recovered P. aeruginosa isolate (P-01) was susceptible to FDC (2 μg/mL), albeit this MIC value was higher than that of a wild-type P. aeruginosa (0.12-0.25 μg/ml). The subsequent isolated strains (P-02, P-03, P-04) displayed increasing levels of FDC MICs (8, 16, and 64 μg/ml, respectively). Those isolates also showed variable and gradual increasing levels of resistance to most β-lactams tested in this study. Surprisingly, no acquired β-lactamase was identified in any of those isolates. Whole-genome sequence analysis suggested that this resistance was driven by multifactorial mechanisms including mutational changes in iron transporter proteins associated with FDC uptake, ampC gene overproduction, and mexAB-oprM overexpression. These findings highlight that a susceptibility testing to FDC must be performed prior to any prescription.

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