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Multidrug-resistant Klebsiella pneumoniae clinical isolates producing NDM- and OXA-type carbapenemase in Nepal.
Takei, Satomi; Tabe, Yoko; Miida, Takashi; Hishinuma, Tomomi; Khasawneh, Abdullah; Kirikae, Teruo; Sherchand, Jeevan B; Tada, Tatsuya.
Affiliation
  • Takei S; Department of Clinical Laboratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Tabe Y; Department of Clinical Laboratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Miida T; Department of Clinical Laboratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Hishinuma T; Department of Microbiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Khasawneh A; Department of Clinical Laboratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Kirikae T; Department of Microbiome Research, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Sherchand JB; Department of Medical Microbiology, Tribhuvan University, Maharajgunj, Kathmandu, Nepal.
  • Tada T; Department of Microbiology, Juntendo University Graduate School of Medicine, Tokyo, Japan. Electronic address: t-tada@juntendo.ac.jp.
J Glob Antimicrob Resist ; 37: 233-243, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38759919
ABSTRACT

OBJECTIVES:

The emergence of multidrug-resistant Klebsiella pneumoniae has become a serious problem in medical settings worldwide.

METHODS:

A total of 46 isolates of multidrug-resistant K. pneumoniae were obtained from 2 hospitals in Nepal from October 2018 to April 2019.

RESULTS:

Most of these isolates were highly resistant to carbapenems, aminoglycosides, and fluoroquinolones with the minimum inhibitory concentrations (MICs) of more than 64 µg/mL. These isolates harboured carbapenemase-encoding genes, including blaNDM-1, blaNDM-5, blaOXA-181 and blaOXA-232, and 16S rRNA methyltransferase-encoding genes, including armA, rmtB, rmtC, and rmtF. Multilocus sequence typing revealed that 44 of 46 isolates were high-risk clones such as ST11 (2%), ST14 (4%), ST15 (11%), ST37 (2%), ST101 (2%), ST147 (28%), ST231 (13%), ST340 (4%), and ST395 (28%). In particular, ST395 isolates, which spread across medical settings in Nepal, co-harboured blaNDM-5 and rmtB on IncFII plasmids and co-harboured blaOXA-181/-232 and rmtF on ColKP3 plasmids. Several isolates harboured blaOXA-181 or blaNDM-5 on their chromosomes and multi-copies of blaNDM-1 or genes encoding 16S rRNA methyltransferases on their plasmids.

CONCLUSIONS:

The presented study demonstrates that the high-risk clones of multidrug-resistant K. pneumoniae spread in a clonal manner across hospitals in Nepal.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Proteins / Beta-Lactamases / Klebsiella Infections / Microbial Sensitivity Tests / Drug Resistance, Multiple, Bacterial / Multilocus Sequence Typing / Klebsiella pneumoniae / Anti-Bacterial Agents Limits: Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: J Glob Antimicrob Resist Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Proteins / Beta-Lactamases / Klebsiella Infections / Microbial Sensitivity Tests / Drug Resistance, Multiple, Bacterial / Multilocus Sequence Typing / Klebsiella pneumoniae / Anti-Bacterial Agents Limits: Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: J Glob Antimicrob Resist Year: 2024 Document type: Article Affiliation country: