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    <title>Saha, S.K.</title>
    <link>http://repub.eur.nl/res/aut/3941/</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>Molecular typing of Salmonella typhi strains from Dhaka (Bangladesh) and development of DNA probes identifying plasmid-encoded multidrug-resistant isolates (Article)</title>
      <link>http://repub.eur.nl/res/pub/8616/</link>
      <pubDate>1996-01-01T00:00:00Z</pubDate>
      <description>Seventy-eight Salmonella typhi strains isolated in 1994 and 1995 from
          patients living in Dhaka, Bangladesh, were subjected to phage typing,
          ribotyping, IS200 fingerprinting, and PCR fingerprinting. The collection
          displayed a high degree of genetic homogeneity, because restricted numbers
          of phage types and DNA fingerprints were observed. A significant number of
          the S. typhi strains (67%) were demonstrated to be multiple drug resistant
          (MDR). The vast majority of the MDR strains were resistant to
          chloramphenicol, ampicillin, trimethoprim, streptomycin, sulfamethoxazole,
          and tetracycline (R type CATmSSuT), a resistance phenotype that has also
          frequently been observed in India. Only two strains displayed a distinct
          MDR phenotype, R type AT-mSSuT. Pulsed-field gel electrophoresis
          demonstrated the presence of large plasmids exclusively in the MDR strains
          of both R types. The plasmids present in the S. typhi strains of R type
          CATmSSuT could be conjugated to Escherichia coli and resulted in the
          complete transfer of the MDR phenotype. PCR fingerprinting allowed
          discrimination of MDR and susceptible strains. The DNA fragments enabling
          discrimination of MDR and susceptible S. typhi strains by PCR were useful
          genetic markers for identifying MDR encoded by large plasmids of the H1
          incompatibility group.</description>
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