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Core/Whole Genome Multilocus Sequence Typing and Core Genome SNP-Based Typing of OXA-48-Producing Klebsiella pneumoniae Clinical Isolates From Spain

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  • Additional Information
    • Contributors:
      Hospital de la Santa Creu i Sant Pau; University of Groningen Groningen; ESCMID Basel; Westfälische Wilhelms-Universität Münster = University of Münster (WWU); Biodiversité et Epidémiologie des Bactéries pathogènes - Biodiversity and Epidemiology of Bacterial Pathogens; Institut Pasteur Paris (IP); This work was partly supported by Interreg IVa, EurSafety Health-net (III-1-02D73), and EurHealth-1Health projects, which are part of a Dutch-German cross-border network supported by the European Commission; the Dutch Ministry of Health, Welfare and Sport (VWS); the Ministry of Economy, Innovation, Digitalisation and Energy of the German Federal State of North Rhine-Westphalia; and the German Federal State of Lower Saxony. BIGSdb-Kp receives institutional funding from Institut Pasteur.
    • Publication Information:
      HAL CCSD
      Frontiers Media
    • Publication Date:
      2020
    • Collection:
      Institut Pasteur: HAL
    • Abstract:
      International audience ; Whole-genome sequencing (WGS)-based typing methods have emerged as promising and highly discriminative epidemiological tools. In this study, we combined gene-by-gene allele calling and core genome single nucleotide polymorphism (cgSNP) approaches to investigate the genetic relatedness of a well-characterized collection of OXA-48-producing Klebsiella pneumoniae isolates. We included isolates from the predominant sequence type ST405 (n = 31) OXA-48-producing K. pneumoniae clone and isolates from ST101 (n = 3), ST14 (n = 1), ST17 (n = 1), and ST1233 (n = 1), obtained from eight Catalan hospitals. Core-genome multilocus sequence typing (cgMLST) schemes from Institut Pasteur's BIGSdb-Kp (634 genes) and SeqSphere+ (2,365 genes), and a SeqSphere+ whole-genome MLST (wgMLST) scheme (4,891 genes) were used. Allele differences or allelic mismatches and the genetic distance, as the proportion of allele differences, were used to interpret the results from a gene-by-gene approach, whereas the number of SNPs was used for the cgSNP analysis. We observed between 0-10 and 0-14 allele differences among the predominant ST405 using cgMLST and wgMLST from SeqSphere+, respectively, and <2 allelic mismatches when using Institut Pasteur's BIGSdb-Kp cgMLST scheme. For ST101, we observed 14 and 54 allele differences when using cgMLST and wgMLST SeqSphere+, respectively, and 2-5 allelic mismatches for BIGSdb-Kp cgMLST. A low genetic distance (<0.0035, a previously established threshold for epidemiological link) was generally in concordance with a low number of allele differences (<8) when using the SeqSphere+ cgMLST scheme. The cgSNP analysis showed 6-29 SNPs in isolates with identical allelic SeqSphere+ cgMLST profiles and 16-61 cgSNPs among ST405 isolates. Furthermore, comparison of WGS-based typing results with previously obtained MLST and pulsed-field gel electrophoresis (PFGE) data showed some differences, demonstrating the different molecular principles underlying these techniques. In conclusion, the ...
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/32082262; pasteur-03329667; https://pasteur.hal.science/pasteur-03329667; https://pasteur.hal.science/pasteur-03329667/document; https://pasteur.hal.science/pasteur-03329667/file/fmicb-10-02961.pdf; PUBMED: 32082262; PUBMEDCENTRAL: PMC7005014
    • Accession Number:
      10.3389/fmicb.2019.02961
    • Online Access:
      https://doi.org/10.3389/fmicb.2019.02961
      https://pasteur.hal.science/pasteur-03329667
      https://pasteur.hal.science/pasteur-03329667/document
      https://pasteur.hal.science/pasteur-03329667/file/fmicb-10-02961.pdf
    • Rights:
      http://creativecommons.org/licenses/by/ ; info:eu-repo/semantics/OpenAccess
    • Accession Number:
      edsbas.A8DBEED6