<?xml version="1.0" encoding="UTF-8" ?>

    <journal>
    <language>en</language>
    <journal_id_issn>2008-2835</journal_id_issn>
    <journal_id_issn_online>2008-4625</journal_id_issn_online>
    <journal_id_pii></journal_id_pii>
    <journal_id_doi></journal_id_doi>
    <journal_id_isnet></journal_id_isnet>
    <journal_id_iranmedex>276</journal_id_iranmedex>
    <journal_id_magiran>5669</journal_id_magiran>
    <journal_id_sid>11181</journal_id_sid>
    <pubdate>
	    <type>gregorian</type>
	    <year>>2022</year>
	    <month>>July-September</month>
	    <day></day>
    </pubdate>
    <volume>14</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_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed></article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>A New Specific DNA Target Sequence for Identification of Staphylococcus epidermidis using Modified Comparative Genomic Analysis</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&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; &lt;em&gt;Staphylococcus epidermidis (S. epidermidis) &lt;/em&gt;is the most frequently isolated pathogen from prostheses infections in the body. &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Therefore, improving its diagnostic methods, including rapid Nucleic Acid Amplification Tests (NAAT), seems necessary. &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Since the first step in designing a NAAT is to find a specific sequence and all DNA targets that have been introduced so far are not completely specific, we introduced a new 100% specific DNA target sequence to identify &lt;em&gt;S. epidermidis &lt;/em&gt;in this study.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p&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; Modified comparative genomic analysis was used to find the best specific target sequence to detect &lt;em&gt;S. epidermidis&lt;/em&gt;. A PCR method was designed for the evaluation of this target. To determine the detection limit and analytical specificity, pure genomic DNA of 18 bacteria include 12 standard strains (one &lt;em&gt;S. epidermidis&lt;/em&gt; and 11 non-&lt;em&gt;S. epidermidis&lt;/em&gt;) and six clinical isolates (five &lt;em&gt;S. epidermidis&lt;/em&gt; and one non-&lt;em&gt;S. epidermidis&lt;/em&gt;) were used.&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; The 400 &lt;em&gt;bp&lt;/em&gt; sequence of &lt;em&gt;S. epidermidis&lt;/em&gt; ATCC 14990 was identified as the most specific sequence (Se400), having a 100% sequence similarity to &lt;em&gt;S. epidermidis&lt;/em&gt; genomes but not with other bacteria. The detection limit of Se400-PCR was 10 &lt;em&gt;fg&lt;/em&gt;, equal to about 4 copies of &lt;em&gt;S. epidermidis&lt;/em&gt; genomic &lt;em&gt;DNA/&amp;mu;l&lt;/em&gt;. All pure DNA templates from &lt;em&gt;S. epidermidis&lt;/em&gt; generated a detectable amplicon by 264 &lt;em&gt;bp&lt;/em&gt; length, but the PCR test was negative for the non-&lt;em&gt;S. epidermidis&lt;/em&gt; group.&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;Conclusion:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The Se400 sequence can be considered as a specific target for detecting &lt;em&gt;S. epidermidis, &lt;/em&gt;based on our findings.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Comparative genomic analysis, Detection, Pathogen, Polymerase chain reaction , Se400, Staphylococcus epidermidis</keyword>
	<start_page>216</start_page>
	<end_page>222</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60507</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60507.pdf</pdf_url>
	<author_list><author><first_name>Reza</first_name><middle_name></middle_name><last_name>Khoshbakht</last_name><suffix></suffix><affiliation>Student Research Committee, Mashhad University of Medical Sciences, Mashahd, Iran</affiliation><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>91887</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Hosna</first_name><middle_name></middle_name><last_name>Zare</last_name><suffix></suffix><affiliation>Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation><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>91888</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Reza</first_name><middle_name></middle_name><last_name>Kamali Kakhki</last_name><suffix></suffix><affiliation>Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation><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>91889</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Alireza</first_name><middle_name></middle_name><last_name>Neshani</last_name><suffix></suffix><affiliation>Department of Laboratory Sciences, School of Paramedical Sciences, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation><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>31529</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Maryam</first_name><middle_name></middle_name><last_name>Arfaatabar</last_name><suffix></suffix><affiliation>Department of Medical Laboratory Sciences, Kashan Branch, Islamic Azad University, Kashan, Iran</affiliation><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>91890</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

