Lab Med Qual Assur 2024; 46(3): 163-166
Published online September 30, 2024
https://doi.org/10.15263/jlmqa.2024.46.3.163
Copyright © Korean Association of External Quality Assessment Service.
Young Ah Kim , Choong Soon Lee , and Kyoung Ja Jang
Department of Laboratory Medicine, National Health Insurance Service Ilsan Hospital, Goyang, Korea
Correspondence to:Young Ah Kim
Department of Laboratory Medicine, National Health Insurance Service Ilsan Hospital, 100 Ilsan-ro, Ilsandong-gu, Goyang 10444, Korea
Tel +82-31-900-0908
E-mail yakim@nhimc.or.kr
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background: The emergence of tigecycline-resistant Acinetobacter baumannii has been reported, and the need for tigecycline susceptibility testing in this strain is increasing. However, neither the Clinical & Laboratory Standards Institute, nor the European Commission on Antimicrobial Susceptibility Testing have provided definitive criteria for tigecycline susceptibility testing of A. baumannii. In this study, the disk diffusion method and the minimal inhibitory concentration (MIC) method were compared to verify conventionally used Food and Drug Administration-identified interpretive criteria to detect tigecycline resistance of A. baumannii.
Methods: Forty-four strains of A. baumannii with tigecycline resistance were collected through the Kor-GLASS (Korean Global Antimicrobial Resistance Surveillance System) study in 2022 using the disk diffusion test (DDT). This strain was retested with the MIC method using a Sensititre Gram Negative GN6F AST plate (Thermo Fisher Scientific, USA) to confirm tigecycline resistance. The confirmed strain was subjected to whole genome analysis to elucidate the tigecycline resistance mechanism.
Results: Only one of the 44 isolates identified as resistant to tigecycline by the DDT showed resistance with the MIC method, thus the concordance rate of the two methods was 2.3% (1/44). Sequence type 195 strain, carrying blaOXA23 was identified. This strain had no resistance genes of the tetracycline family but had resistance genes to other antimicrobial families.
Conclusions: Discrepancy of the tigecycline susceptibility test of A. baumannii was identified. To detect tigecycline resistance of A. baumannii, more reliable methods are required.
Keywords: Acinetobacter baumannii, Tigecycline, Susceptibility, Minimal inhibitory concentration method, Disk diffusion test
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