First report of a carbapenemase OXA-48-producing Hafnia alvei clinical isolate
- PMID: 37424558
- PMCID: PMC10323787
- DOI: 10.1099/acmi.0.000498.v3
First report of a carbapenemase OXA-48-producing Hafnia alvei clinical isolate
Abstract
Introduction: Carbapenems are usually used in the treatment of infections caused by cephalosporin-resistant Enterobacterales ; however, the increase in carbapenem-resistant Enterobacterales (CRE) has become one of the most important problems in public health. Hafnia alvei is associated with intestinal and extraintestinal infections, especially in patients with any chronic disease or some type of immunosupression. H. alvei is resistant to first-generation aminopenicillins and cephalosporins owing to the β-lactamase (Amp C) in their chromosome; the only carbapenem-resistant Hafnia strain described until now was due to a lack of the OmpK36 protein that plays an important role in permeability to carbapenems.
Case presentation: We present the case of a 65-year-old male diagnosed with acute lithiasic cholecystitis. Culture of the biliary prosthesis yielded a OXA-48-producing H. alvei that was identified by MALDI-TOF (matrix-assisted laser desorption/ionization-time of flight) MS. Carbapenemase production was detected by immunochromatography and confirmed by sequencing.
Conclusion: To our knowledge, this is the first report of OXA-48-producing H. alvei probably obtained by horizontal transfer from Enterobacter cloacae OXA-48 isolated in previous samples.
Keywords: Hafnia alvei; OXA-48; carbapenem; carbapenemase.
© 2023 The Authors.
Conflict of interest statement
The authors declare that there are no conflicts of interest.
Figures
References
-
- Katchanov J, Asar L, Klupp E-M, Both A, Rothe C, et al. Carbapenem-resistant Gram-negative pathogens in a German university medical center: Prevalence, clinical implications and the role of novel β-lactam/β-lactamase inhibitor combinations. PLoS One. 2018;13:e0195757. doi: 10.1371/journal.pone.0195757. - DOI - PMC - PubMed
Publication types
LinkOut - more resources
Full Text Sources