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    <title>Messer, S.</title>
    <link>http://repub.eur.nl/res/aut/7133/</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>
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    <item>
      <title>Food-initiated outbreak of methicillin-resistant Staphylococcus aureus analyzed by pheno- and genotyping (Article)</title>
      <link>http://repub.eur.nl/res/pub/8537/</link>
      <pubDate>1995-01-01T00:00:00Z</pubDate>
      <description>An outbreak of methicillin-resistant Staphylococcus aureus (MRSA)
          involving 27 patients and 14 health-care workers (HCW) was studied. The
          outbreak started in the hematology unit of the University Hospital
          Rotterdam, Dijkzigt, The Netherlands, and spread to the surgical unit.
          Twenty-one patients (77.8%) developed clinical disease, and five died.
          Subsequently, MRSA was detected in food and in the throat of one of the
          HCW who prepared food for hematology patients. Food contaminated by an HCW
          most likely caused the first case of MRSA septicemia. This route of
          transmission has not been described before. The outbreak strain was
          probably transmitted to the surgical unit by a colonized nurse, where it
          caused an explosive outbreak. Airborne probably transmitted to the
          surgical unit by a colonized nurse, where it caused an explosive outbreak.
          Airborne MRSA transmission played an important role in disseminating the
          organism. The outbreak was controlled within 6 months by intensifying
          surveillance, temporarily closing the affected wards, treating carriers,
          and instituting an MRSA ward outside the hospital. Phage typing, insertion
          sequence probing, protein A gene typing, and DNA fingerprinting by PCR
          revealed that all outbreak-related isolates were identical. By
          pulsed-field gel electrophoresis, all but one of the outbreak-related
          isolates were determined to be identical. Protein A gene typing identified
          numerous (11) repeat units in all outbreak-related isolates, which
          supports the suggestion that the outbreak strain may have been more
          virulent and more transmissible than other MRSA strains. Pheno- and
          genotyping studies underlined the value of DNA fingerprinting methods for
          investigation of MRSA epidemiology. Optimal discriminatory power was
          achieved by combining the results of four genotyping methods.</description>
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