Literature DB >> 26968884

Whole-genome typing and characterization of blaVIM19-harbouring ST383 Klebsiella pneumoniae by PFGE, whole-genome mapping and WGS.

Julia S Sabirova1, Basil Britto Xavier1, Jasmine Coppens1, Olympia Zarkotou2, Christine Lammens1, Lore Janssens1, Ronald Burggrave3, Trevor Wagner3, Herman Goossens1, Surbhi Malhotra-Kumar4.   

Abstract

OBJECTIVES: We utilized whole-genome mapping (WGM) and WGS to characterize 12 clinical carbapenem-resistant Klebsiella pneumoniae strains (TGH1-TGH12).
METHODS: All strains were screened for carbapenemase genes by PCR, and typed by MLST, PFGE (XbaI) and WGM (AflII) (OpGen, USA). WGS (Illumina) was performed on TGH8 and TGH10. Reads were de novo assembled and annotated [SPAdes, Rapid Annotation Subsystem Technology (RAST)]. Contigs were aligned directly, and after in silico AflII restriction, with corresponding WGMs (MapSolver, OpGen; BioNumerics, Applied Maths).
RESULTS: All 12 strains were ST383. Of the 12 strains, 11 were carbapenem resistant, 7 harboured blaKPC-2 and 11 harboured blaVIM-19. Varying the parameters for assigning WGM clusters showed that these were comparable to STs and to the eight PFGE types or subtypes (difference of three or more bands). A 95% similarity coefficient assigned all 12 WGMs to a single cluster, whereas a 99% similarity coefficient (or ≥10 unmatched-fragment difference) assigned the 12 WGMs to eight (sub)clusters. Based on a difference of three or more bands between PFGE profiles, the Simpson's diversity indices (SDIs) of WGM (0.94, Jackknife pseudo-values CI: 0.883-0.996) and PFGE (0.93, Jackknife pseudo-values CI: 0.828-1.000) were similar (P = 0.649). However, the discriminatory power of WGM was significantly higher (SDI: 0.94, Jackknife pseudo-values CI: 0.883-0.996) than that of PFGE profiles typed on a difference of seven or more bands (SDI: 0.53, Jackknife pseudo-values CI: 0.212-0.849) (P = 0.007).
CONCLUSIONS: This study demonstrates the application of WGM to understanding the epidemiology of hospital-associated K. pneumoniae. Utilizing a combination of WGM and WGS, we also present here the first longitudinal genomic characterization of the highly dynamic carbapenem-resistant ST383 K. pneumoniae clone that is rapidly gaining importance in Europe.
© The Author 2016. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

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Year:  2016        PMID: 26968884     DOI: 10.1093/jac/dkw003

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  3 in total

1.  Evidence of Sharing of Klebsiella pneumoniae Strains between Healthy Companion Animals and Cohabiting Humans.

Authors:  Cátia Marques; Adriana Belas; Catarina Aboim; Patrícia Cavaco-Silva; Graça Trigueiro; Luís Telo Gama; Constança Pomba
Journal:  J Clin Microbiol       Date:  2019-05-24       Impact factor: 5.948

2.  Remarkable Genome Stability among emm1 Group A Streptococcus in Belgium over 19 Years.

Authors:  Jasmine Coppens; Basil Britto Xavier; Katherine Loens; Christine Lammens; Margareta Ieven; Veerle Matheeussen; Herman Goossens; Surbhi Malhotra-Kumar
Journal:  Genome Biol Evol       Date:  2019-05-01       Impact factor: 3.416

3.  Whole-Genome Comparative Analysis of Two Carbapenem-Resistant ST-258 Klebsiella pneumoniae Strains Isolated during a North-Eastern Ohio Outbreak: Differences within the High Heterogeneity Zones.

Authors:  María Soledad Ramirez; Gang Xie; German M Traglia; Shannon L Johnson; Karen W Davenport; David van Duin; Azam Ramazani; Federico Perez; Michael R Jacobs; David J Sherratt; Robert A Bonomo; Patrick S G Chain; Marcelo E Tolmasky
Journal:  Genome Biol Evol       Date:  2016-07-03       Impact factor: 3.416

  3 in total

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