Antibiotics (Nov 2022)

Characterisation of Non-Carbapenemase-Producing Carbapenem-Resistant <i>Klebsiella pneumoniae</i> Based on Their Clinical and Molecular Profile in Malaysia

  • Yee Qing Lee,
  • Sasheela Sri La Sri Ponnampalavanar,
  • Chun Wie Chong,
  • Rina Karunakaran,
  • Kumutha Malar Vellasamy,
  • Kartini Abdul Jabar,
  • Zhi Xian Kong,
  • Min Yi Lau,
  • Cindy Shuan Ju Teh

DOI
https://doi.org/10.3390/antibiotics11111670
Journal volume & issue
Vol. 11, no. 11
p. 1670

Abstract

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Non-carbapenemase-producing carbapenem-resistant Klebsiella pneumoniae (NC-CRKP) confers carbapenem resistance through a combination of chromosomal mutations and acquired non-carbapenemase resistance mechanisms. In this study, we aimed to evaluate the clinical and molecular profiles of NC-CRKP isolated from patients in a tertiary teaching hospital in Malaysia from January 2013 to October 2019. During the study period, 54 NC-CRKP-infected/colonised patients’ isolates were obtained. Clinical parameters were assessed in 52 patients. The all-cause in-hospital mortality rate among NC-CRKP patients was 46.2% (24/52). Twenty-three (44.2%) patients were infected, while others were colonised. Based on the Charlson Comorbidity Index (CCI) score, 92.3% (48/52) of the infected/colonised patients had a score of ≥ 1. Resistance genes found among the 54 NC-CRKP isolates were blaTEM, blaSHV, blaCTX-M, blaOXA, and blaDHA. Porin loss was detected in 25/54 (46.3%) strains. None of the isolated strains conferred carbapenem resistance through the efflux pumps system. In conclusion, only 25/54 (46.3%) NC-CRKP conferred carbapenem resistance through a combination of porin loss and the acquisition of non-carbapenemase resistance mechanisms. The carbapenem resistance mechanisms for the remaining strains (53.7%) should be further investigated as rapid identification and distinction of the NC-CRKP mechanisms enable optimal treatment and infection control efforts.

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