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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">ajmb60517</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>Evaluation of PLGA-Encapsulated Recombinant GroEL of S. typhi immune  Responses Against Enterohaemorrhagic and Enteropathogenic Escherichia coli</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Parvane </surname><given-names>Milad</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Nazarian</surname><given-names>Shahram</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Kordbacheh</surname><given-names>Emad</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Fathi</surname><given-names>Javad</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Minae </surname><given-names>Mohamad Ebrahim</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Ramezani </surname><given-names>Mohammad 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>14</volume>
      <issue>4</issue>
      <fpage>294</fpage>
      <lpage>302</lpage>
      <history>
        <date date-type="received">
          <day>18</day>
          <month>9</month>
          <year>2021</year>
        </date>
        <date date-type="accepted">
          <day>16</day>
          <month>7</month>
          <year>2022</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;font-size:9.5pt&quot;&gt;Background:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; Heat Shock Proteins (HSPs) elicit humoral and cellular immune responses. Due to their high sequence homology, they can be developed as a new immunogen for cross prophylactic and vaccination effects against infectious agents such as Enteropathogenic and Enterohemorrhagic &lt;em&gt;Escherichia coli&lt;/em&gt; (EPEC and EHEC). This study aimed to evaluate the immunogenicity and cross-protective efficacy of rGroEL of &lt;em&gt;&lt;span style=&quot;background-color:white&quot;&gt;Salmonella typhi&lt;/span&gt;&lt;/em&gt; (&lt;em&gt;S. typhi&lt;/em&gt;) encapsulated in poly lactic-co-glycolic acid (PLGA) nanoparticles against EPEC and EHEC.&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;span style=&quot;font-size:9.5pt&quot;&gt;Methods:&lt;/span&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;Recombinant GroEL was expressed in &lt;em&gt;Escherichia coli&lt;/em&gt; (&lt;em&gt;E. coli&lt;/em&gt;) and purified using Ni-NTA affinity chromatography. The protein was encapsulated in PLGA by the double emulsion method, and the nanoparticles were characterized physicochemically. BALB/c mice were immunized, and the efficacy of the protein to elicit immune responses was assessed. &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;span style=&quot;font-size:9.5pt&quot;&gt;Results:&lt;/span&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;Over-expression in &lt;em&gt;E. coli&lt;/em&gt; led to corresponding 64.5 &lt;em&gt;kDa&lt;/em&gt; protein bands in Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE). Non-ag-gregated nanoparticles had a spherical shape with a mean diameter of 194.3&amp;plusmn;3 &lt;em&gt;nm&lt;/em&gt; and encapsulation efficiency of 89.5&amp;plusmn;2.5%. Antibody isotyping revealed that GroEL immunization induced both IgG1 and IgG2a antibodies. Moreover, immunization of the mice with recombinant GroEL protein conferred 80 and 60% protection against lethal infections by EPEC and EHEC, respectively. Furthermore, organ burden studies revealed a significant reduction in infection in the immunized mice compared to the non-immunized ones. Passive immunization with anti-GroEL sera also protected 50% of the mice against the lethal doses of EHEC and EPEC strains. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;font-size:9.5pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The findings indicated that immunization of the mice with recombinant GroEL of &lt;em&gt;S. typhi&lt;/em&gt; elicited cross-protection against other bacterial infections. This represented the immense potential of GroEL to be developed as a single vaccine against multiple pathogens&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

      </p>
      </abstract>
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