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. 2022 Nov 15;66(11):e0064822.
doi: 10.1128/aac.00648-22. Epub 2022 Oct 26.

Emergence of KPC-31, a KPC-3 Variant Associated with Ceftazidime-Avibactam Resistance, in an Extensively Drug-Resistant ST235 Pseudomonas aeruginosa Clinical Isolate

Affiliations

Emergence of KPC-31, a KPC-3 Variant Associated with Ceftazidime-Avibactam Resistance, in an Extensively Drug-Resistant ST235 Pseudomonas aeruginosa Clinical Isolate

Diego Faccone et al. Antimicrob Agents Chemother. .

Abstract

A ceftazidime-avibactam-resistant KPC-producing Pseudomonas aeruginosa strain was isolated in Argentina from a tracheal aspirate. The patient was treated with ceftazidime-avibactam in combination with other agents for 130 days. Whole-genome sequencing of P. aeruginosa identified a D179Y substitution in the Ω loop of KPC-3, corresponding to KPC-31, integrated at the chromosome. The strain belonged to the sequence type 235/O11 (ST235/O11) high-risk clone. Evaluation of carbapenemase detection assays most used by clinical laboratories failed to identify the isolate as a KPC producer.

Keywords: KPC; Pseudomonas aeruginosa; ceftazidime-avibactam resistance; extensively drug-resistant ST235.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

FIG 1
FIG 1
Chromosomal location of blaKPC-31 in P. aeruginosa M27432. Comparison with plasmid pGM116-005_01 from K. pneumoniae DFSAN054110 and the chromosome of P. aeruginosa AR_0357 suggests a plasmidic origin of an ~19-kb fragment containing blaKPC-31. The light blue regions between DNA sequences indicate nucleotide identity >99 by BLASTn. Arrows indicate predicted open reading frames (ORFs). Red arrows represent blaKPC gene variants.

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