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    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Avicenna J Med Biotech</journal-id>
      <journal-id journal-id-type="publisher-id">arij002</journal-id>
      <journal-title-group>
        <journal-title>Avicenna Journal of Medical Biotechnology</journal-title>
      </journal-title-group>
      <issn pub-type="ppub">2008-2835</issn>
      <issn pub-type="epub">2008-4625</issn>
      <publisher>
        <publisher-name>Avicenna Research Institute</publisher-name>
      </publisher>
    </journal-meta>

    <article-meta>
      <article-id pub-id-type="publisher-id">ajmb60536</article-id>
      <article-id pub-id-type="doi"></article-id>
      <article-id pub-id-type="pmid"></article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
             <subject></subject> 
        </subj-group>
        <subj-group>
            <subject></subject>
        </subj-group> 
      </article-categories>
      <title-group>
        <article-title>Development of a High Sensitive Multiplex Lateral Flow Immunoassay (LFIA) System  for Rapid Detection of Methicillin-Resistant Staphylococcus Aureus (MRSA)</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Amini</surname><given-names>Masoomeh</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Pourmand </surname><given-names>Mohammad Reza</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Faridi-Majidi </surname><given-names>Reza</given-names></name></contrib></contrib-group>
      <pub-date pub-type="ppub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <pub-date pub-type="epub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <volume>15</volume>
      <issue>2</issue>
      <fpage>100</fpage>
      <lpage>107</lpage>
      <history>
        <date date-type="received">
          <day>11</day>
          <month>5</month>
          <year>2022</year>
        </date>
        <date date-type="accepted">
          <day>10</day>
          <month>2</month>
          <year>2023</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background: &lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methicillin-resistant &lt;em&gt;Staphylococcus aureus&lt;/em&gt; (MRSA) has become a worldwide concern as an epidemic bacterium and a cause of nosocomial and community-acquired infections. One of the major problems in the prevention and treatment of infections caused by MRSA strains is their multi-drug resistant trait, which causes the spread of infections and increases the mortality rate. Therefore, a rapid and accurate method is needed to identify MRSA strains, initiate appropriate antibiotic&amp;nbsp;therapy, and control its infection. The aim of this study was to develop a twin lateral flow immunoassay system to detect methicillin-resistant &lt;em&gt;Staphylococcus aureus &lt;/em&gt;(MRSA).&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; First, BSA blocked AuNPs-anti&lt;em&gt;-&lt;/em&gt;peptidoglycan antibody and AuNPs-anti-BSA antibody were used to detect &lt;em&gt;Staphylococcus aureus &lt;/em&gt;(&lt;em&gt;S. aureus&lt;/em&gt;). Then, AuNPs&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;-anti-PBP2a antibody was used to specifically detect &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;MRSA. Sensitivity, specificity and limit of detection of this twin immunoassay system were assessed using &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;MRSA, &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;methicillin susceptible &lt;em&gt;S. aureus &lt;/em&gt;and clinical samples. Results &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;were compared to those of cefoxitin disc diffusion (FOX30) and Polymerase Chain Reaction (PCR) as gold standards.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;The Limit of Detection&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; (LOD) of this twin system &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;were 10&lt;sup&gt;3&lt;/sup&gt; and 10&lt;sup&gt;4&lt;/sup&gt; CFU/&lt;em&gt;ml&lt;/em&gt; for the first and second strips, respectively. Sensitivity and specificity of this innovative assay in detecting MRSA were 92.30 and 97.36%, compared to &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;FOX30 and PCR, respectively. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p&gt;&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; High rates of sensitivity and specificity of this initiative system show its high potentials for rapid and accurate detection of MRSA.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

      </p>
      </abstract>
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