4.4 Article

Clonal change of carbapenem-resistant Acinetobacter baumannii isolates in a Korean hospital

Journal

INFECTION GENETICS AND EVOLUTION
Volume 93, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.meegid.2021.104935

Keywords

A; baumannii; Carbapenems; Sequence type; Antimicrobial resistance; Resistant gene

Funding

  1. Korea Centers for Disease Control and Prevention [2019-ER5501-01]
  2. Korea Health Promotion Institute [2019-ER5501-01] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The study investigated 96 CRAB isolates from a Korean hospital between 2016 and 2018, identifying clonal complex 208 as predominant. ST208 isolates showed higher resistance rates to minocycline, while ST369 isolates exhibited lower resistance rates to aminoglycosides and trimethoprim/sulfamethoxazole. Additionally, the study revealed evolutionary changes in CRAB isolates related to the emergence of new sequence types and selection of resistant genes.
The expansion of specific carbapenem-resistant Acinetobacter baumannii (CRAB) clones is a global concern due to its therapeutic difficulty and epidemicity. To understand the prevalence of CRAB isolates in a Korean hospital, we investigated the epidemiological characteristics of 96 CRAB isolates between 2016 and 2018, including the sequence types (STs), antimicrobial susceptibility, and genetic background of resistance to carbapenems and aminoglycosides. Six STs were identified using the Oxford multilocus sequence typing scheme; ST191 (n = 8), ST208 (n = 12), ST229 (n = 11), and ST369 (n = 21) were previously identified clones in the study hospital, whereas gpi variants of ST208, ST451 (n = 34) and ST784 (n = 10), were emerging clones. ST208 isolates exhibited higher resistance rates to minocycline than other ST isolates, whereas ST369 isolates exhibited lower resistance rates to aminoglycosides and trimethoprim/sulfamethoxazole than other ST isolates. All CRAB isolates previously isolated in the study hospital carried ISAbaI-blaOXA-23 for carbapenem resistance, but 10 ST229 isolates carried only ISAbaI-blaOXA-51. The carriage of armA was lower in ST369 isolates (38%) than in other ST isolates (>= 83%). The frequency and diversity of aminoglycoside-modifying enzyme genes were decreased among the CRAB isolates between 2016 and 2018 compared with CRAB isolates between 2013 and 2015 at the study hospital. In conclusion, clonal complex 208 CRAB isolates are predominant in the study hospital. This study demonstrates the evolutionary change of CRAB isolates in the study hospital in relation to the emergence of new STs and selection of resistant genes.

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