<?xml version="1.0"?>
<Articles JournalTitle="Journal of Medical Bacteriology">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Journal of Medical Bacteriology</JournalTitle>
      <Issn>2251-8649</Issn>
      <Volume>1</Volume>
      <Issue>1-2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>12</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Prevalence and Evaluation of Toxin Genes among Uropathogenic Escherichia coli Clinical Isolates by Duplex PCR</title>
    <FirstPage>17</FirstPage>
    <LastPage>22</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Javad</FirstName>
        <LastName>Saraylu</LastName>
        <affiliation locale="en_US">Department of Microbiology, Faculty of Basic Sciences, Minoodasht Branch, Islamic Azad University, Minoodasht, IR Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Jalil</FirstName>
        <LastName>Fallah-Mehrabadi</LastName>
        <affiliation locale="en_US">Department of Microbiology, Faculty of Basic Sciences, Minoodasht Branch, Islamic Azad University, Minoodasht, IR Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Abbas Ali</FirstName>
        <LastName>Imani-Fooladi</LastName>
        <affiliation locale="en_US">Applied Microbiology Research Center, Baqiyatallah University of Medical Sciences, Tehran, IR Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Aylar</FirstName>
        <LastName>Sabbaghi</LastName>
        <affiliation locale="en_US">R &amp; D Laboratory of Molecular Biology, Gene Fanavaran Company, Tehran, IR Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hedrosha</FirstName>
        <LastName>Molla-Aghamirzaei</LastName>
        <affiliation locale="en_US">R &amp; D Laboratory of Molecular Biology, Gene Fanavaran Company, Tehran, IR Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohsen</FirstName>
        <LastName>Hasankhani</LastName>
        <affiliation locale="en_US">Clinical Pathology Laboratory, Omid Hospital, Abhar, IR Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>12</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>12</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background:&#xA0; One of the most common infections in human is urinary tract infection &#xA0;(UTI) &#xA0;and &#xA0;Uropathogenic &#xA0;Escherichia &#xA0;coli &#xA0;is&#xA0; one &#xA0;of &#xA0;its &#xA0;major causative agents. UTI is extremely common among young women. Children under age 5 are also highly at risk. Considering the prevalence of this disease, it is necessary &#xA0;to design&#xA0; an appropriate &#xA0;diagnostic &#xA0;method &#xA0;for its effective diagnosis. &#xA0;The aim of present &#xA0;study was to identify&#xA0; the prevalence &#xA0;of two virulence genes (sat and vat) among Uropathogenic E. coli isolates.
Methods: Urine samples were taken from 350 patients with urinary tract infection. The samples were cultured on EMB agar and Blood agar. The suspected E. coli colonies were isolated and confirmed by biochemical tests. The genomic DNA was extracted from 297 isolated E. coli and target genes were amplified &#xA0;by PCR. The amplicons &#xA0;were sequenced &#xA0;and analyzed&#xA0; with ClustalW &#xA0;software. &#xA0;Moreover, &#xA0;data analysis&#xA0; was performed &#xA0;by using SPSS software.&#xA0; &#xA0;Subsequently,&#xA0; &#xA0;Duplex&#xA0; &#xA0;PCR&#xA0; &#xA0;was&#xA0;&#xA0; optimized&#xA0; &#xA0;for&#xA0;&#xA0; simultaneous detection of two genes.
Results: The prevalence of sat and vat genes were 75 (n: 225) and 36 (n: 106)percent, &#xA0;respectively. &#xA0;In addition, &#xA0;less &#xA0;than &#xA0;4% &#xA0;(n: 11) &#xA0;of&#xA0; clinical &#xA0;isolates comprised two genes.
Conclusion: According to the conducted research, molecular identification of Uropathogenic E .coli strains according to detection of sat gene is potentially an appropriate method and could be noted for diagnosis.</abstract>
    <web_url>https://jmb.tums.ac.ir/index.php/jmb/article/view/6</web_url>
    <pdf_url>https://jmb.tums.ac.ir/index.php/jmb/article/download/6/4</pdf_url>
  </Article>
</Articles>
