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High interlaboratory reproducibility of DNA sequence-based typing of bacteria in a multicenter study

  • M. Aires-De-Sousa
  • , K. Boye
  • , H. De Lencastre
  • , A. Deplano
  • , M. C. Enright
  • , J. Etienne
  • , A. Friedrich
  • , D. Harmsen*
  • , A. Holmes
  • , X. W. Huijsdens
  • , Angela Kearns
  • , A. Mellmann
  • , H. Meugnier
  • , J. K. Rasheed
  • , E. Spalburg
  • , B. Strommenger
  • , M. J. Struelens
  • , F. C. Tenover
  • , J. Thomas
  • , U. Vogel
  • H. Westh, J. Xu, W. Witte
*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    193 Citations (Scopus)

    Abstract

    Current DNA amplification-based typing methods for bacterial pathogens often lack interlaboratory reproducibility. In this international study, DNA sequence-based typing of the Staphylococcus aureus protein A gene (spa, 110 to 422 bp) showed 100% intra- and interlaboratory reproducibility without extensive harmonization of protocols for 30 blind-coded S. aureus DNA samples sent to 10 laboratories. Specialized software for automated sequence analysis ensured a common typing nomenclature.

    Original languageEnglish
    Pages (from-to)619-621
    Number of pages3
    JournalJournal of Clinical Microbiology
    Volume44
    Issue number2
    DOIs
    Publication statusPublished - Feb 2006

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