<?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>10.61186/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>1397</year>
	<month>4</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2018</year>
	<month>7</month>
	<day>1</day>
</pubdate>
<volume>12</volume>
<number>4</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>fa</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Dissemination of Class 1 Integron among Different Multidrug Resistant Pseudomonas aeruginosa Strains </title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa>تحقيقي</content_type_fa>
	<content_type>Original Paper</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div&gt;&lt;strong&gt;ABSTRACT &lt;/strong&gt;&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Background and objectives:&lt;/strong&gt; The present study was conducted to detect class 1 integrons and evaluate antibiotic susceptibility patterns among clinical isolates of &lt;em&gt;P. aeruginosa&lt;/em&gt;.&lt;br&gt;
&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;strong&gt;Methods:&lt;/strong&gt; Sixty clinical samples from blood, tracheal wounds, burns and urinary tract infections were collected from three general hospitals in Tehran, Iran. Culture of specimens was performed on common bacteriological culture media. Bacteria were &amp;nbsp;identified based on mobility, pigment production, growth at 42 &lt;sup&gt;o&lt;/sup&gt;C, and oxidase and catalase tests. Overall, 21 &lt;em&gt;P.&amp;nbsp; aeruginosa&lt;/em&gt; strains were isolated&lt;span dir=&quot;RTL&quot;&gt;.&lt;/span&gt; Antimicrobial susceptibility of was evaluated via the disk diffusion method (Kirby-Bauer) according to the CLSI guidelines. Presence of the &lt;em&gt;intI1&lt;/em&gt;, &lt;em&gt;sul1&lt;/em&gt;, &lt;em&gt;aadA2 &lt;/em&gt;and &lt;em&gt;aadB&lt;/em&gt; gene cassettes was investigated using PCR. The collected&amp;nbsp;data were analyzed using SPSS&amp;nbsp;software (version 21).&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Results:&lt;/strong&gt; The most effective antimicrobial agents against &lt;em&gt;P. aeruginosa&lt;/em&gt; isolates were tetracycline and gentamicin. All &lt;em&gt;P. aeruginosa &lt;/em&gt;isolates were multidrug re&amp;shy;sistant. Moreover, the &lt;em&gt;intI1&lt;/em&gt;, &lt;em&gt;sul1&lt;/em&gt;, &lt;em&gt;aadA2&lt;/em&gt; and &lt;em&gt;aadB&lt;/em&gt; genes were found in 90.5%, 90.5%, 47.6% and 19% of the &lt;em&gt;P. aeruginosa&lt;/em&gt; isolates, respectively.&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Conclusion:&lt;/strong&gt; The results indicate that the presence of &lt;em&gt;aadB, aadA2&lt;/em&gt; and &lt;em&gt;sul1&lt;/em&gt; gene cassetes may play an important role in the dissemination of antimicrobial resistance determinants.&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Keywords:&lt;/strong&gt; &lt;em&gt;Pseu&amp;shy;domonas aeruginosa&lt;/em&gt;, integron, multidrug resistance.

&lt;div&gt;&lt;strong&gt;ABSTRACT &lt;/strong&gt;&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Background and objectives:&lt;/strong&gt; The present study was conducted to detect class 1 integrons and evaluate antibiotic susceptibility patterns among clinical isolates of &lt;em&gt;P. aeruginosa&lt;/em&gt;.&lt;br&gt;
&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;strong&gt;Methods:&lt;/strong&gt; Sixty clinical samples from blood, tracheal wounds, burns and urinary tract infections were collected from three general hospitals in Tehran, Iran. Culture of specimens was performed on common bacteriological culture media. Bacteria were &amp;nbsp;identified based on mobility, pigment production, growth at 42 &lt;sup&gt;o&lt;/sup&gt;C, and oxidase and catalase tests. Overall, 21 &lt;em&gt;P.&amp;nbsp; aeruginosa&lt;/em&gt; strains were isolated&lt;span dir=&quot;RTL&quot;&gt;.&lt;/span&gt; Antimicrobial susceptibility of was evaluated via the disk diffusion method (Kirby-Bauer) according to the CLSI guidelines. Presence of the &lt;em&gt;intI1&lt;/em&gt;, &lt;em&gt;sul1&lt;/em&gt;, &lt;em&gt;aadA2 &lt;/em&gt;and &lt;em&gt;aadB&lt;/em&gt; gene cassettes was investigated using PCR. The collected&amp;nbsp;data were analyzed using SPSS&amp;nbsp;software (version 21).&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Results:&lt;/strong&gt; The most effective antimicrobial agents against &lt;em&gt;P. aeruginosa&lt;/em&gt; isolates were tetracycline and gentamicin. All &lt;em&gt;P. aeruginosa &lt;/em&gt;isolates were multidrug re&amp;shy;sistant. Moreover, the &lt;em&gt;intI1&lt;/em&gt;, &lt;em&gt;sul1&lt;/em&gt;, &lt;em&gt;aadA2&lt;/em&gt; and &lt;em&gt;aadB&lt;/em&gt; genes were found in 90.5%, 90.5%, 47.6% and 19% of the &lt;em&gt;P. aeruginosa&lt;/em&gt; isolates, respectively.&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Conclusion:&lt;/strong&gt; The results indicate that the presence of &lt;em&gt;aadB, aadA2&lt;/em&gt; and &lt;em&gt;sul1&lt;/em&gt; gene cassetes may play an important role in the dissemination of antimicrobial resistance determinants.&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Keywords:&lt;/strong&gt; &lt;em&gt;Pseu&amp;shy;domonas aeruginosa&lt;/em&gt;, integron, multidrug resistance.

&lt;div&gt;&lt;strong&gt;ABSTRACT &lt;/strong&gt;&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Background and objectives:&lt;/strong&gt; The present study was conducted to detect class 1 integrons and evaluate antibiotic susceptibility patterns among clinical isolates of &lt;em&gt;P. aeruginosa&lt;/em&gt;.&lt;br&gt;
&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;strong&gt;Methods:&lt;/strong&gt; Sixty clinical samples from blood, tracheal wounds, burns and urinary tract infections were collected from three general hospitals in Tehran, Iran. Culture of specimens was performed on common bacteriological culture media. Bacteria were &amp;nbsp;identified based on mobility, pigment production, growth at 42 &lt;sup&gt;o&lt;/sup&gt;C, and oxidase and catalase tests. Overall, 21 &lt;em&gt;P.&amp;nbsp; aeruginosa&lt;/em&gt; strains were isolated&lt;span dir=&quot;RTL&quot;&gt;.&lt;/span&gt; Antimicrobial susceptibility of was evaluated via the disk diffusion method (Kirby-Bauer) according to the CLSI guidelines. Presence of the &lt;em&gt;intI1&lt;/em&gt;, &lt;em&gt;sul1&lt;/em&gt;, &lt;em&gt;aadA2 &lt;/em&gt;and &lt;em&gt;aadB&lt;/em&gt; gene cassettes was investigated using PCR. The collected&amp;nbsp;data were analyzed using SPSS&amp;nbsp;software (version 21).&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Results:&lt;/strong&gt; The most effective antimicrobial agents against &lt;em&gt;P. aeruginosa&lt;/em&gt; isolates were tetracycline and gentamicin. All &lt;em&gt;P. aeruginosa &lt;/em&gt;isolates were multidrug re&amp;shy;sistant. Moreover, the &lt;em&gt;intI1&lt;/em&gt;, &lt;em&gt;sul1&lt;/em&gt;, &lt;em&gt;aadA2&lt;/em&gt; and &lt;em&gt;aadB&lt;/em&gt; genes were found in 90.5%, 90.5%, 47.6% and 19% of the &lt;em&gt;P. aeruginosa&lt;/em&gt; isolates, respectively.&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Conclusion:&lt;/strong&gt; The results indicate that the presence of &lt;em&gt;aadB, aadA2&lt;/em&gt; and &lt;em&gt;sul1&lt;/em&gt; gene cassetes may play an important role in the dissemination of antimicrobial resistance determinants.&lt;br&gt;
&lt;strong&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Keywords:&lt;/strong&gt; &lt;em&gt;Pseu&amp;shy;domonas aeruginosa&lt;/em&gt;, integron, multidrug resistance.&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword> Pseu‌domonas aeruginosa, integron, multidrug resistance.</keyword>
	<start_page>36</start_page>
	<end_page>42</end_page>
	<web_url>http://mlj.goums.ac.ir/browse.php?a_code=A-10-1-527&amp;slc_lang=fa&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Zahra</first_name>
	<middle_name></middle_name>
	<last_name>Salimizadeh</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></email>
	<code>100319475328460014506</code>
	<orcid>100319475328460014506</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Microbiology, Faculty of Bioscience, Islamic Azad University, North Tehran Branch, Tehran, Iran </affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Seyed Masoud </first_name>
	<middle_name></middle_name>
	<last_name>Hashemi Karouei </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></email>
	<code>100319475328460014507</code>
	<orcid>100319475328460014507</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of biology, Babol Branch Islamic Azad University, Babol, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Farzaneh</first_name>
	<middle_name></middle_name>
	<last_name>Hosseini</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>farzaneh953@yahoo.com</email>
	<code>100319475328460014508</code>
	<orcid>100319475328460014508</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Microbiology, Faculty of Bioscience, Islamic Azad University, North Tehran Branch, Tehran, Iran </affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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