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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">ajmb221</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>Interferences in the Optimization of the MTT Assay for Viability Estimation of  Proteus mirabilis</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Grela</surname><given-names>Ewa</given-names></name></contrib><aff>Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Ząbek</surname><given-names>Adam</given-names></name></contrib><aff>Department of Pathology, Khatam Al Anbia Hospital, Tehran, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Grabowiecka</surname><given-names>Agnieszka</given-names></name></contrib><aff>Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran</aff></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>7</volume>
      <issue>4</issue>
      <fpage>159</fpage>
      <lpage>165</lpage>
      <history>
        <date date-type="received">
          <day>23</day>
          <month>2</month>
          <year>2015</year>
        </date>
        <date date-type="accepted">
          <day>1</day>
          <month>6</month>
          <year>2015</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p&gt;Background: The chromogenic assay based on MTT bioreduction was adapted to &lt;em&gt;Proteus mirabilis viability&lt;/em&gt; estimations. We primarily intended to use the assay for the evaluation of novel antimicrobial compounds, including structures with possible permeabilizing activity. Therefore, the influence of basic permeabilizing agents like Triton X-100 and EDTA upon the MTT assay was studied.&lt;br /&gt;
Methods: 3-(4,5-Dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) was used as a substrate for the whole-cell dehydrogenase activity estimations. The amount of formazan product was evaluated in the end-point reactions terminated with acidic isopropanol or in the continuous reactions run in the presence of low detergent concentrations.&lt;br /&gt;
Results: The generally established procedure of the end product dissolution with acidic isopropanol caused absorbance instability which strongly affected the results accuracy. The disadvantage was especially pronounced when the assay was conducted in Mueller-Hinton Broth. PBS with 0.01% Triton X-100 used as the reaction medium allowed to omit the formazan dissolution step and follow the microbial MTT reduction in a continuous mode. It was observed that in Proteus mirabilis with a compromised outer membrane the assay score was artificially increased above the untreated control.&lt;br /&gt;
Conclusion: The dependence of the assay results on the cell integrity might be a major drawback of the MTT assay application for the evaluation of novel antimicrobials against Gram-negative microorganisms. On the other hand, the MTT reduction could be conveniently used to assay the permeabilization degree in biotechnological protocols.&lt;/p&gt;

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      </abstract>
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