<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Medical Laboratory Journal</title>
<title_fa>Medical Laboratory Journal</title_fa>
<short_title>mljgoums</short_title>
<subject>Medical Sciences</subject>
<web_url>http://mlj.goums.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn></journal_id_issn>
<journal_id_issn_online>2538-4449</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.66224/mlj</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1405</year>
	<month>4</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2026</year>
	<month>7</month>
	<day>1</day>
</pubdate>
<volume>20</volume>
<number>3</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Optimum culture conditions for achieving enhanced biofilm formation 
and high-level icaA transcription in Staphylococcus aureus</title>
	<subject_fa>ميکروب شناسي</subject_fa>
	<subject>Microbiology</subject>
	<content_type_fa>Research Article</content_type_fa>
	<content_type>Research Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;&lt;span style=&quot;font-size:12px;&quot;&gt;&lt;span style=&quot;font-family:Times New Roman;&quot;&gt;&lt;b&gt;Background:&lt;/b&gt; Biofilm formation in &lt;i&gt;Staphylococcus aureus&lt;/i&gt; (&lt;i&gt;S. aureus&lt;/i&gt;), mediated by the &lt;i&gt;ica&lt;/i&gt; operon, is a key virulence factor. This study examined how different glucose-supplemented broth culture media influence biofilm production and &lt;i&gt;ica&lt;/i&gt; gene expression in &lt;i&gt;S. aureus&lt;/i&gt;.&lt;br&gt;
&lt;b&gt;Methods:&lt;/b&gt; The phenotypic ability to adhere to a polystyrene surface and produce a slime layer was evaluated using the microtiter plate test (MtP) and Congo red tube test, respectively. Using PCR, the presence of the intercellular adhesion (&lt;i&gt;ica&lt;/i&gt;) locus in &lt;i&gt;S. aureus&lt;/i&gt; strains was confirmed. Subsequently, quantitative real-time RT-PCR was performed to investigate &lt;i&gt;icaA&lt;/i&gt; transcription in various media, including tryptic soy broth (TSB), brain-heart infusion broth (BHIB), nutrient broth (NB), and Mueller-Hinton broth (MHB), containing 0, 0.25, 0.5, 1, and 2% glucose.&lt;br&gt;
&lt;b&gt;Results:&lt;/b&gt; Our results showed that although all studied strains adhered to the wells of polystyrene microtiter plates, the optimal rate of biofilm formation was observed in TSB medium containing 1% glucose. However, biofilm formation was not significantly different in NB, MHB, and BHIB media. Supplementation of all media with 1% glucose resulted in the highest biofilm production, and &lt;i&gt;icaA&lt;/i&gt; transcription increased in all media after glucose addition up to 1%.&lt;br&gt;
&lt;b&gt;Conclusion&lt;/b&gt;: The results of the present study indicated that TSB medium supplemented with 1% glucose was the most appropriate medium for evaluating biofilm formation by &lt;i&gt;S. aureus&lt;/i&gt; isolates.&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Biofilm, Staphylococcus aureus, Culture Media, Glucose, Quantitative Real Time PCR</keyword>
	<start_page>0</start_page>
	<end_page>0</end_page>
	<web_url>http://mlj.goums.ac.ir/browse.php?a_code=A-10-1738-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Aram </first_name>
	<middle_name></middle_name>
	<last_name>Sharifi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>a.sharifi@uok.ac.ir</email>
	<code>100319475328460032943</code>
	<orcid>100319475328460032943</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Animal Science, Faculty of Agriculture, University of Kurdistan, Sanandaj, Kurdistan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Abdolmajid </first_name>
	<middle_name></middle_name>
	<last_name>Mohammadzadeh</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>mohammadzadeh@basu.ac.ir</email>
	<code>100319475328460032944</code>
	<orcid>100319475328460032944</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Bu-Ali Sina University, Hamedan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Pezhman </first_name>
	<middle_name></middle_name>
	<last_name>Mahmoodi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>mahmoodi_pezhman@yahoo.com</email>
	<code>100319475328460032945</code>
	<orcid>100319475328460032945</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Bu-Ali Sina University, Hamedan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Taghi  </first_name>
	<middle_name></middle_name>
	<last_name>Zahraei Salehi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>tsalehi@ut.ac.ir</email>
	<code>100319475328460032946</code>
	<orcid>100319475328460032946</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
