NDM-5-producing Klebsiella pneumoniae ST258 in a university hospital in Argentina.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
23 Sep 2024
Historique:
received: 28 05 2024
accepted: 09 09 2024
medline: 23 9 2024
pubmed: 23 9 2024
entrez: 23 9 2024
Statut: aheadofprint

Résumé

A drastic increase in carbapenem resistance among Klebsiella pneumoniae isolates occurred during the period 2019-22. Three epidemiological changes could be evidenced: (i) NDM became the predominant carbapenemase; (ii) NDM-5 replaced NDM-1; and (iii) the emergence of NDM-producing K. pneumoniae ST258 (NDM-KpST258). Carbapenem-resistant K. pneumoniae isolates from patients on the ICU of a university hospital of Buenos Aires were studied during the period 2019-22. Identification was performed by MS and susceptibility by the Phoenix system (broth microdilution for colistin). Carbapenemase production was detected phenotypically. Molecular studies included PCR with specific primers and WGS (in some isolates). NDM-producing K. pneumoniae was statistically associated with the use of ceftazidime/avibactam between 2019 and April 2021, whereas in the period from May 2021 to December 2022, it seemed to be related to the presence of NDM-5-KpST258. A gradual increase in the number of urease-negative NDM-Kp-ST258 during 2019-22 was observed. The plasmid origin of NDM-5 was supported by its presence on the IncFII incompatibility group plasmid. Our study describes the first outbreak of NDM5-KpST258 at an ICU in Argentina, remarkably associated with considerable changes in the carbapenemase epidemiology. The intrinsic characteristics of ST258 may contribute to increased spread of NDM in hospital settings, resembling KPC-2 dissemination.

Sections du résumé

BACKGROUND BACKGROUND
A drastic increase in carbapenem resistance among Klebsiella pneumoniae isolates occurred during the period 2019-22. Three epidemiological changes could be evidenced: (i) NDM became the predominant carbapenemase; (ii) NDM-5 replaced NDM-1; and (iii) the emergence of NDM-producing K. pneumoniae ST258 (NDM-KpST258).
MATERIALS AND METHODS METHODS
Carbapenem-resistant K. pneumoniae isolates from patients on the ICU of a university hospital of Buenos Aires were studied during the period 2019-22. Identification was performed by MS and susceptibility by the Phoenix system (broth microdilution for colistin). Carbapenemase production was detected phenotypically. Molecular studies included PCR with specific primers and WGS (in some isolates).
RESULTS RESULTS
NDM-producing K. pneumoniae was statistically associated with the use of ceftazidime/avibactam between 2019 and April 2021, whereas in the period from May 2021 to December 2022, it seemed to be related to the presence of NDM-5-KpST258. A gradual increase in the number of urease-negative NDM-Kp-ST258 during 2019-22 was observed. The plasmid origin of NDM-5 was supported by its presence on the IncFII incompatibility group plasmid.
CONCLUSIONS CONCLUSIONS
Our study describes the first outbreak of NDM5-KpST258 at an ICU in Argentina, remarkably associated with considerable changes in the carbapenemase epidemiology. The intrinsic characteristics of ST258 may contribute to increased spread of NDM in hospital settings, resembling KPC-2 dissemination.

Identifiants

pubmed: 39310949
pii: 7765179
doi: 10.1093/jac/dkae337
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : UBACYT
ID : 20020220300060BA

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Carla Alvarez (C)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Marcela Nastro (M)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Beatriz Goyheneche (B)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Nicolás Potente (N)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Martin Ledesma (M)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Carlos Vay (C)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Thierry Naas (T)

Team ReSIST, UMR1184, INSERM, Université Paris-Saclay, CEA, School of Medicine, LabEx LERMIT, Le Kremlin-Bicêtre, France.
Bacteriology-Hygiene unit, Bicêtre Hospital, APHP Paris-Saclay, Le Kremlin-Bicêtre, France.
French National Reference Center for Antibiotic Resistance: Carbapenemase-producing Enterobacterales, Le Kremlin-Bicêtre, France.

Mónica Foccoli (M)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Stella de Gregorio (S)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Angela Famiglietti (A)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Laura Dabos (L)

Centro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid (UPM)-Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA/CSIC), Pozuelo de Alarcón (Madrid), Campus de Montegancedo UPM, Madrid 28223, Spain.

Carlos Hernán Rodriguez (CH)

Universidad de Buenos Aires, Departamento de Bioquímica Clínica, Avenida Córdoba 2351, Buenos Aires City 1120, Argentina.

Classifications MeSH