Prevalence, clonal diversity, and antimicrobial resistance of hypervirulent Klebsiella pneumoniae and Klebsiella variicola clinical isolates in northern Japan.


Journal

Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 16 06 2023
revised: 27 07 2023
accepted: 10 08 2023
medline: 4 12 2023
pubmed: 22 8 2023
entrez: 21 8 2023
Statut: ppublish

Résumé

Hypervirulent Klebsiella pneumoniae (hvKp) and Klebsiella variicola (hvKv) cause hospital/community-acquired infections, often associated with antimicrobial resistance (AMR). This study aimed to investigate the molecular epidemiology of hvKp and hvKv in northern Japan. A total of 500 K. pneumoniae and 421 K. variicola clinical isolates collected from August to December 2021 were studied. Prevalence of virulence factor-encoding genes, wzi sequence and associated K/KL type, sequence type (ST), and beta-lactamases and their types were characterized. Any virulence gene (rmpA, rmpA2, peg-344, iucA, iutA, and iroB) and/or magA was detected in 25% (n = 125) of K. pneumoniae and 1% (n = 5) of K. variicola. Among these hvKp/hvKv, 22 wzi types (18 and 4 types, respectively) and 24 STs (20 and 4 STs, respectively) were identified. Sequence types of hvKp were classified into some clonal groups (CGs), among which CG35, including six STs, was the most common (n = 59; 47%), followed by CG23, and CG65. ST268 (CG35) associated with wzi95-K20 or wzi720 was the dominant lineage (n = 43, 34%), while K1:ST23/ST249 and K2:ST65/ST86 accounted for 26% and 13% of hvKp, respectively. Extended-spectrum beta-lactamase (ESBL) genes (blaCTX-M-2, blaCTX-M-3, blaCTX-M-15, and blaCTX-M-27) were detected in only ST23 and CG35 (ST268 and ST412) hvKp. No isolate was resistant to carbapenems, without detection of the ESBL gene in K. variicola. Phylogenetically, wzi was differentiated into two main clusters of K. pneumoniae and K. variicola. A major clonal group CG347 was identified in K. variicola. Clonal structures were revealed for hvKp and hvKv clinical isolates with their AMR status in northern Japan.

Identifiants

pubmed: 37604276
pii: S2213-7165(23)00135-2
doi: 10.1016/j.jgar.2023.08.009
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Bacterial Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

11-18

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Auteurs

Norifumi Matsuda (N)

Department of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Meiji Soe Aung (MS)

Department of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan. Electronic address: meijisoeaung@sapmed.ac.jp.

Noriko Urushibara (N)

Department of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Mitsuyo Kawaguchiya (M)

Department of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Nobuhide Ohashi (N)

Department of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Kenji Taniguchi (K)

Sapporo Clinical Laboratory, Inc., Sapporo, Hokkaido, Japan.

Kenji Kudo (K)

Sapporo Clinical Laboratory, Inc., Sapporo, Hokkaido, Japan.

Masahiko Ito (M)

Sapporo Clinical Laboratory, Inc., Sapporo, Hokkaido, Japan.

Nobumichi Kobayashi (N)

Department of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

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Classifications MeSH