4.4 Article

Dynamics and molecular features of OXA-48-like-producing Klebsiella pneumoniae lineages in a Tunisian hospital

Journal

JOURNAL OF GLOBAL ANTIMICROBIAL RESISTANCE
Volume 20, Issue -, Pages 87-93

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jgar.2019.07.005

Keywords

Klebsiella pneumoniae; OXA-48; OXA-204; Sequence type; Tunisia

Funding

  1. French Agency for Food, Environmental and Occupational Health Safety (ANSES)
  2. Ministere de l'Enseignement Superieur et de la Recherche Scientifique in Tunisia

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Objectives: The aim of this study was to elucidate the molecular features of genes, plasmids and clones of OXA-48-like producing Klebsiella pneumoniae isolates recovered in Sahloul Hospital (Sousse, Tunisia) in the period 2012-2014. Methods: In vitro antimicrobial susceptibility testing, S1 nuclease pulsed-field gel electrophoresis (S1-PFGE), Southern blotting and PCR-based replicon typing (PBRT) were performed. Extended-spectrum beta-lactamase (ESBL) and carbapenemases genes were detected by PCR and sequencing. The clonality of isolates was assessed by PFGE and multilocus sequence typing (MLST). Results: Klebsiella pneumoniae accounted for 26.8% (1095/4083) of clinical Enterobacterales isolates identified during 2012-2014, of which 21.9% (240/1095) were resistant to carbapenems, mostly harbouring bla(OXA-48-like) genes (196/240; 81.7%). Plasmid analysis showed that bla(OXA-204) and bla(OXA-48) were mostly carried by IncA/C and IncL plasmids, respectively. The current data highlight the dominance of two ST101 and ST147 lineages spreading OXA-48 and OXA-204, respectively, through successive clonal spreads at this hospital. In addition, a large diversity of other K. pneumoniae lineages was also identified, such as ST15, ST36 and ST525 spreading OXA-48 as well as ST340, ST2032, ST301, ST199 and ST1561 spreading OXA-48 or OXA-204, constituting a reservoir of possible dominant clones in the future. Conclusion: This study reports the full molecular characterisation of carbapenem resistance in K. pneumoniae and the predominance of a few clones responsible for the dissemination of OXA-48 and OXA-204 enzymes in a Tunisian hospital. (C) 2019 International Society for Antimicrobial Chemotherapy. Published by Elsevier Ltd.

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