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<Articles JournalTitle="Iranian Journal of Microbiology">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>6</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2014</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Multiplex real-time PCR assay for detection and differentiation of Bordetella pertussis and Bordetella parapertussis</title>
    <FirstPage>140</FirstPage>
    <LastPage>148</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Valentina</FirstName>
        <LastName>Kolodkina</LastName>
        <affiliation locale="en_US">Republican Research &amp; Practical Centre for Epidemiology and Microbiology, Minsk, Belarus.</affiliation>
      </Author>
      <Author>
        <FirstName>Vladimir</FirstName>
        <LastName>Martinov</LastName>
        <affiliation locale="en_US">Republican Research &amp; Practical Centre for Epidemiology and Microbiology, Minsk, Belarus.</affiliation>
      </Author>
      <Author>
        <FirstName>Andrey</FirstName>
        <LastName>Babenko</LastName>
        <affiliation locale="en_US">N. N. Aleksandrov Republican Scientific and Practical Centre of Oncology and Medical Radiology, Minsk, Belarus.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>16</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objective: Rapid diagnosis of pertussis is important for the timely isolation of the infection source and early prevention measures among the contact persons, especially among non-vaccinated infants for whom pertussis is life- threatening.
Materials and Methods: Targets IS481, IS1001, BP0026 and human GAPDH gene were used to develop a multiplex real- time PCR assay based on the TaqMan technology for detection and identification of Bordetella pertussis and Bordetella parapertussis in clinical samples. A total of 121 human clinical specimens obtained within 2012-2013 were used to evaluate the multiplex real-time PCR assay. Clinical specimens were also tested for culture and conventional PCR. Sensitivity and specificity for culture, conventional PCR, and multiplex real-time PCR were measured in comparison with a clinical standard for B. pertussis infection.
Results: The lower limit of detection (LLOD) of the multiplex assay was similar to the LLOD of each target in an individual assay format, which was approximately 1 genomic equivalent per reaction for IS481, IS1001 and 10 genomic equivalents per reaction for BP0026 target. When the B. pertussis assays were compared with a clinical standard for B. pertussis infection, sensitivity was 5, 59 and 89% the specificity was 100, 100 and 100% for culture, conventional PCR, and multiplex real-time PCR, respectively.
Conclusions: Developed multiplex real-time PCR offers a fast tool with high sensitivity and specificity for the diagnosis of B. pertussis and B. parapertussis infections which is suitable for implementation in a routine laboratory diagnostics.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/429</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/429/206</pdf_url>
  </Article>
</Articles>
