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    <title>Velden, J. van der</title>
    <link>http://repub.eur.nl/res/aut/23888/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Validation of binary typing for Staphylococcus aureus strains (Article)</title>
      <link>http://repub.eur.nl/res/pub/9015/</link>
      <pubDate>1999-01-01T00:00:00Z</pubDate>
      <description>Most of the DNA-based methods for genetic typing of Staphylococcus aureus
          strains generate complex banding patterns. Therefore, we have developed a
          binary typing procedure involving strain-differentiating DNA probes which
          were generated on the basis of randomly amplified polymorphic DNA (RAPD)
          analysis. We present and validate the usefulness of 15 DNA probes,
          according to generally accepted performance criteria for molecular typing
          systems. RAPD analysis with multiple primers was performed on 376 S.
          aureus strains of which 97% were methicillin resistant (MRSA). Among the
          1,128 RAPD patterns generated, 66 were selected which identified 124
          unique DNA fragments. From these amplicons, only 12% turned out to be
          useful for isolate-specific binary typing. The nature of the
          RAPD-generated DNA fragments was investigated by partial DNA sequence
          analysis. Several homologies with known S. aureus sequences and with genes
          from other species were discovered; however, 87% of the probe sequences
          are of previously unknown origin. The locations of most of the DNA probes
          on the chromosome of S. aureus NCTC 8325 were determined by hybridization.
          Seven fragments were randomly dispersed along the genome, five were
          clustered within the 2500- to 2600-kb position of the genome, and the
          remaining four did not recognize complementary sequences in S. aureus NCTC
          8325. A total of 103 S. aureus strains (69% MRSA) were used for the
          validation of the binary typing technique. The 15 DNA probes provided
          stable epidemiological markers, both in vitro (type consistency after
          serial passages on culture media) and in vivo (comparison of sequential
          isolates recovered from cases of persistent colonization). The
          discriminatory power of binary typing (D = 0.998) exceeded that of
          pulsed-field gel electrophoresis (D = 0.966) and RAPD analysis (D =
          0.949). Reproducibility, measured by analyzing multiple strains belonging
          to a multitude of different epidemiological clusters, was comparable to
          that of other genotyping techniques used. Contribution of the DNA probes
          to the discriminatory power of the system was analyzed by comparison of
          dendrograms. This study demonstrates that binary typing is a robust tool
          for the genetic typing of S. aureus isolates.</description>
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