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OXA-48-Like-Producing Klebsiella pneumoniae in Southern Spain in 2014-2015
Jesús Machuca1,2,3, Lorena López-Cerero4,2,3,5, Felipe Fernández-Cuenca1,2,3
1Unidad de Enfermedades Infecciosas, Microbiología y Medicina Preventiva, Hospital Universitario Virgen Macarena, Seville, Spain.
Abstract:
The aim of this study was to characterize the population structure of 56 OXA-48-like-producing Klebsiella pneumoniae isolates, as well as extended-spectrum β-lactamase (ESBL) and carbapenemase genes, recovered in 2014 and 2015 from 16 hospitals in southern Spain. XbaI pulsed-field gel electrophoresis and multilocus sequence typing were performed to assess clonal relatedness. Representative isolates belonging to OXA-48-like-producing and CTX-M-15-coproducing pulsotypes were selected for characterization of blaOXA-48-like- and blaCTX-M-15-carrying plasmids by PCR-based replicon typing, IncF subtyping, whole-genome sequencing analysis, and typing of Tn1999 structures. Forty-three OXA-48-producing isolates (77%) were recovered from clinical samples and 13 from rectal swabs. All isolates showed ertapenem MIC values of ≥1 mg/liter, although 70% remained susceptible to imipenem and meropenem. Forty-nine isolates (88%) produced OXA-48, 5 produced OXA-245, and 2 produced OXA-181. Twenty-eight different pulsotypes (5 detected in more than 1 hospital) and 16 sequence types (STs) were found. The most prevalent clones were ST15 (29 isolates [52%]) and ST11 (7 isolates [13%]). Forty-five (80%) isolates were also blaCTX-M-15 carriers. The blaCTX-M-15 gene was mostly (82%) located on IncR plasmids, although ST15 and ST11 isolates also carried this gene on IncF plasmids. The composite transposon variant Tn1999.2-like was the most frequent. Among ST15 and ST11 isolates, different transposon variants were observed. The blaOXA-48 gene was mainly located on IncL plasmids, although IncM plasmids were also observed. The spread of OXA-48-like-producing K. pneumoniae in southern Spain is mainly due to ST15 and ST11 clones. Variation within clonal lineages could indicate different acquisition events for both ESBL and carbapenemase traits.
Insights
The spread of OXA-48-like carbapenemase-producing Klebsiella pneumoniae in Spain is primarily driven by ST15 and ST11 clones. These clones carry both carbapenemase and extended-spectrum beta-lactamase genes on various plasmids.
Area of Science:
- Microbiology
- Genetics
- Epidemiology
Background:
- Carbapenemase-producing Enterobacteriaceae (CPE) pose a significant global health threat.
- OXA-48-like carbapenemases are increasingly reported in Klebsiella pneumoniae.
- Understanding the population structure and genetic elements is crucial for controlling CPE spread.
Purpose of the Study:
- To characterize the population structure of OXA-48-like-producing Klebsiella pneumoniae isolates from southern Spain.
- To identify the co-occurrence of extended-spectrum beta-lactamase (ESBL) and carbapenemase genes.
- To analyze the genetic elements, including plasmids and transposons, carrying these resistance genes.
Main Methods:
- Pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) for population structure analysis.
- Whole-genome sequencing (WGS) for detailed genetic characterization.
- Plasmid analysis including PCR-based replicon typing and IncF subtyping.
- Typing of Tn1999 transposon structures.
Main Results:
- Fifty-six OXA-48-like-producing K. pneumoniae isolates were analyzed from 16 hospitals.
- ST15 (52%) and ST11 (13%) were the most prevalent clones, responsible for the spread.
- 80% of isolates also carried the blaCTX-M-15 gene (ESBL).
- blaOXA-48-like genes were mainly on IncL plasmids, while blaCTX-M-15 was often on IncR and IncF plasmids.
- Tn1999.2-like was the most frequent transposon variant.
Conclusions:
- The spread of OXA-48-like-producing K. pneumoniae in southern Spain is predominantly driven by ST15 and ST11 clones.
- These successful clones harbor both carbapenemase and ESBL genes, facilitating co-selection and spread.
- Variations within these clonal lineages suggest multiple acquisition events for resistance genes.
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