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Author Spotlight: Advancing Antibiotic Resistance Research Using an Efflux-Deficient Bacterial Strain and a Single-Copy Gene Expression System
Published on: January 5, 2024
Chromosomal co-carriage of blaOXA-23 and blaOXA-500 in a carbapenem-resistant Acinetobacter pittii isolate
Md Shohel Rana1, Je Chul Lee2, Shukho Kim3
1Department of Microbiology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.
Abstract:
Carbapenem resistance in non-baumannii Acinetobacter has been increasingly reported worldwide. This study investigated the genetic basis of carbapenem resistance in Acinetobacter pittii isolate KBN12P06770 carrying blaOXA-23 and blaOXA-500 using whole-genome sequencing. Two carbapenemase genes were located on the chromosome. Two copies of blaOXA-23 located on Tn2006 were identified. Additional chromosomally encoded antimicrobial resistance genes, including blaADC-18 and ant(3")-IIc, as well as efflux pump genes (adeIJK, adeFGH, abeM, and abaQ), were identified, with the exception of plasmid-borne ant(2")-Ia. qPCR analysis revealed that the blaOXA-23 was more highly expressed than blaOXA-500. Notably, blaOXA-23 featured the Ser225Pro substitution, first characterized in this study, which may enhance β-lactamase activity based on structural modeling. Furthermore, multilocus sequence typing (MLST) assigned KBN12P06770 to ST1611 within clonal complex 63 (CC63), with close clustering to ST2737 indicating recent divergence. The comprehensive genomic analysis of A. pittii isolate KBN12P06770 highlights the complex genetic architecture underlying carbapenem resistance.

