4.7 Article

Clinical and molecular characterization of Acinetobacter seifertii in Taiwan

Journal

JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Volume 76, Issue 2, Pages 312-321

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jac/dkaa432

Keywords

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Funding

  1. Taipei Veterans General Hospital [V106B-002, V107C-037, V108C-012, V109C-012, VTA106-T-5-3, VTA107-T-3-2, VTA108-T-2-3, VTA109-T-3-2]
  2. Tri-Service General Hospital [TSGH-C107-099, TSGH-C108-137, TSGH-C109-144, VTA108-T-2-2]
  3. National Defense Medical Center [MAB-107-095, MAB-108-038]
  4. Ministry of Science and Technology [MOST 105-2314-B-016-039-MY3, MOST 107-2314-B-075-066-MY3, MOST 107-2314-B-016-051-MY3, MOST 108-2314-B-016-029, MOST 108-2320-B-038-053]

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Acinetobacter seifertii, a new member of the Acinetobacter baumannii group, is a causative agent of severe infections in humans. This study investigated the clinical and molecular characteristics of A. seifertii in 80 adults with bloodstream infection over an 8 year period. The main source of A. seifertii BSI was the respiratory tract, with high mortality rates. Levofloxacin and carbapenems show potential as treatment options, while colistin resistance mechanisms were not associated with specific gene variations. Transmissibility of carbapenem resistance determinants was also observed in various species within the Acinetobacter group. Close monitoring of A. seifertii is warranted.
Objectives: Acinetobacter seifertii, a new member of the Acinetobacter baumannii group, has emerged as a cause of severe infections in humans. We investigated the clinical and molecular characteristics of A. seifertii. Patients and methods: This retrospective study enrolled 80 adults with A. seifertii bloodstream infection (BSI) at four medical centres over an 8 year period. Species identification was confirmed by MALDI-TOF MS, rpoB sequencing and WGS. Molecular typing was performed by MLST. Clinical information, antimicrobial susceptibility and the mechanisms of carbapenem and colistin resistance were analysed. Transmissibility of the carbapenem-resistance determinants was examined by conjugation experiments. Results: The main source of A. seifertii BSI was the respiratory tract (46.3%). The 28 day and in-hospital mortality rates of A. seifertii BSI were 18.8% and 30.0%, respectively. High APACHE II scores and immunosuppressant therapy were independent risk factors for 28 day mortality. The most common MLST type was ST553 (58.8%). Most A. seifertii isolates were susceptible to Levofloxacin (86.2%), and only 37.5% were susceptible to colistin. Carbapenem resistance was observed in 16.3% of isolates, mostly caused by the plasmid-borne ISAba1-bla(OXA-51) Like genetic structure. A. seifertii could transfer various carbapenem-resistance determinants to A. baumannii, Acinetobacter nosocomialis and other A. seifertii isolates. Variations of pmrCAB and lpxCAD genes were not associated with colistin resistance of A. seifertii. Conclusions: Levofloxacin and carbapenems, but not colistin, have the potential to be the drug of choice for A. seifertii infections. A. seifertii can transfer carbapenem-resistance determinants to other species of the A. baumannii group and warrants close monitoring.

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