<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Public Health">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>37</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2008</Year>
        <Month>09</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Single Strand Conformation Polymorphism analysis of PCR-amplified rDNA to differentiate medically important Aspergillus Species</title>
    <FirstPage>52</FirstPage>
    <LastPage>59</LastPage>
    <AuthorList>
      <Author>
        <FirstName>K</FirstName>
        <LastName>Diba</LastName>
        <affiliation locale="en_US">Dept. of  Parasitology and Mycology, School of Public Health and Institute of Public Health Research</affiliation>
      </Author>
      <Author>
        <FirstName>SH</FirstName>
        <LastName>Mirhendi</LastName>
        <affiliation locale="en_US">Dept. of  Parasitology and Mycology, School of Public Health and Institute of Public Health Research</affiliation>
      </Author>
      <Author>
        <FirstName>P</FirstName>
        <LastName>Kordbacheh</LastName>
        <affiliation locale="en_US">Dept. of  Parasitology and Mycology, School of Public Health and Institute of Public Health Research</affiliation>
      </Author>
      <Author>
        <FirstName>N</FirstName>
        <LastName>Jalalizand</LastName>
        <affiliation locale="en_US">Laboratory of Molecular Biology, Esfehan Research Center of Public Health, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Aspergillus species are associated with allergic bronchopulmonary disease, mycotic keratitis, otomycosis, na&#xAD;sal sinusitis and invasive infection. In this study, we developed a PCR-Single Strand Confomational Polymorphism method to identify the most common Aspergillus species and we showed some advantages of this method comparing a PCR-Restric&#xAD;tion Fragment Length Polymorphism with our designed restriction enzyme. 
Methods: We selected ITS2, as a short fragment within the rDNA region (length size: 330 bp) to be amplified as small size PCR product. We mixed 5 ml of the PCR product with an equal volume of loading buffer and followed by incubation for 5 min at 95&#xBA; C and quenching in an ice bath. The mixture was applied to a 6%-12% Gradient Poly acryl amide gel to run in a verti&#xAD;cal electrophoresis, then gel was stained with ethidium bromide and silver nitrate which followed by an ethidium bro&#xAD;mide staining. 
Results: Our results of restriction digestion showed a fine identification of 7 tested Aspergillus species dur&#xAD;ing 5-6 hours af&#xAD;ter an overnight mycelial growth. As our results some of tested Aspergillus species: A. nidulans, A. fisheri, A. quad&#xAD;ricincta, (A. fumigatus and A. niger) as a group and (A. flavus, A. tereus and A. ochraceus) as another group, can be dis&#xAD;criminated. More&#xAD;over SSCP analysis enabled us to identify above Aspergillus species within 8-12 h after an over night growth without us&#xAD;ing an expensive restriction enzyme.
Conclusion: It is concluded that Single Strand Conformational Polymorphism is a simple and rapid method for identifica&#xAD;tion of some medically important Aspergillus.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/2034</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/2034/2015</pdf_url>
  </Article>
</Articles>
