<?xml version="1.0"?>
<Articles JournalTitle="Journal of Arthropod-Borne Diseases">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Journal of Arthropod-Borne Diseases</JournalTitle>
      <Issn>2322-1984</Issn>
      <Volume>12</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2018</Year>
        <Month>08</Month>
        <Day>07</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Cross-Genera PCR Amplification of DNA from Apicomplexan Parasites</title>
    <FirstPage>321</FirstPage>
    <LastPage>324</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Philippe Gil de</FirstName>
        <LastName>Mendon&#xE7;a</LastName>
        <affiliation locale="en_US">Institute of Comparative Tropical Medicine and Parasitology, Ludwig Maximilian University, Munich, Germany</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>08</Month>
        <Day>07</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>08</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: The discovery of an unexpected genetic sequence raised doubts about the specificity of a primer pair targeting Babesia spp. and Theileria spp. This study aimed to check the specificity of this primer pair.
Methods: Conventional end-point PCR and real-time PCR protocols using primers targeting the 18S rRNA gene V4 hypervariable region of Babesia spp. and Theileria spp. were tested for potential cross-genera amplification using DNA from a palette of parasitic protists and pathogenic bacteria as a template. These investigations took place at the Ludwig Maximilian University of Munich (Germany) in 2010 as part of the EDEN project.
Results: Successful amplification was obtained with DNA from five apicomplexan genera: Babesia, Theileria, Hepa&#xAD;tozoon, Toxoplasma, and Hammondia. No amplicons were obtained when DNA from Leishmania infantum or bacte&#xAD;ria within the genera Borrelia, Leptospira or Anaplasma was used as a template.
Conclusion: This cross-genera amplification ability is useful for the quick exclusion of many parasite species from PCR negative diagnostic samples. Accurate species identification from PCR positive samples requires genetic se&#xAD;quencing of the amplicon.</abstract>
    <web_url>https://jad.tums.ac.ir/index.php/jad/article/view/956</web_url>
    <pdf_url>https://jad.tums.ac.ir/index.php/jad/article/download/956/413</pdf_url>
  </Article>
</Articles>
